Highly validated and characterized monoclonal/polyclonal
antibodies and recombinant
proteins
The majority of AAA Biotech’s antibodies are highly validated and can be use in multiple
applications such as ELISA, FC,
ICC, IF, IHC, IP, WB, etc. We have antibodies available for rare species, in multiple conjugated
forms or recombinant
antibodies.
As for our high quality proteins, the majority have 90% purity, detected by SDS-PAGE while some are
available in
different tags such as Flag, GST, His, MBP, etc. We also carry high quality native and biologically
active proteins.
AAA Biotech is constantly working to expand our capacity to provide recombinant proteins and
antibodies to most
target proteins.
SELECT `p`.*, `pd`.*, IFNULL(pdns.ncbi_summary, "N/A") as ncbi_summary_pdns, IFNULL(pdns.sp_comments, "N/A") as sp_comments_pdns, IFNULL(pdns.ncbi_research_articles, "N/A") as ncbi_research_articles_pdns, IFNULL(pe.products_description_extra, "N/A") as products_description_extra
FROM (`products`, `products` as `p`)
LEFT OUTER JOIN `products_description` as `pd` ON `p`.`products_id` = `pd`.`products_id`
LEFT OUTER JOIN `products_description_ncbi_sp` as `pdns` ON `p`.`products_id` = `pdns`.`products_id`
LEFT OUTER JOIN `products_extra` as `pe` ON `p`.`products_id` = `pe`.`products_id`
WHERE `p`.`products_id` = '29913'
AND `pd`.`language_id` = 1
LIMIT 1
Query
Database
1.82 ms
select p.*, pd.*,
ifnull(pdns.ncbi_summary, 'N/A') as ncbi_summary_pdns,
ifnull(pdns.sp_comments, 'N/A') as sp_comments_pdns,
ifnull(pdns.ncbi_research_articles, 'N/A') as ncbi_research_articles_pdns,
ifnull(pe.products_description_extra, 'N/A') as products_description_extra
from products p
LEFT OUTER JOIN products_description pd on p.products_id = pd.products_id
LEFT OUTER JOIN products_description_ncbi_sp pdns on p.products_id = pdns.products_id
LEFT OUTER JOIN products_extra pe on p.products_id = pe.products_id
where p.products_id = '29913' and pd.language_id = 1
Query
Database
1.32 ms
SELECT `options_values_price` as `price`, `products_options_values_name` as `package`
FROM `products_attributes`
JOIN `products_options_values` ON `products_options_values`.`products_options_values_id` = `products_attributes`.`options_values_id`
WHERE `products_attributes`.`products_id` = '29913'
Database (4 total Queries, 4 of them unique across 2 Connections)
Time
Query String
2.13 ms
SELECT `p`.*, `pd`.*, IFNULL(pdns.ncbi_summary, "N/A") as ncbi_summary_pdns, IFNULL(pdns.sp_comments, "N/A") as sp_comments_pdns, IFNULL(pdns.ncbi_research_articles, "N/A") as ncbi_research_articles_pdns, IFNULL(pe.products_description_extra, "N/A") as products_description_extra
FROM (`products`, `products` as `p`)
LEFT OUTER JOIN `products_description` as `pd` ON `p`.`products_id` = `pd`.`products_id`
LEFT OUTER JOIN `products_description_ncbi_sp` as `pdns` ON `p`.`products_id` = `pdns`.`products_id`
LEFT OUTER JOIN `products_extra` as `pe` ON `p`.`products_id` = `pe`.`products_id`
WHERE `p`.`products_id` = '29913'
AND `pd`.`language_id` = 1
LIMIT 1
select p.*, pd.*,
ifnull(pdns.ncbi_summary, 'N/A') as ncbi_summary_pdns,
ifnull(pdns.sp_comments, 'N/A') as sp_comments_pdns,
ifnull(pdns.ncbi_research_articles, 'N/A') as ncbi_research_articles_pdns,
ifnull(pe.products_description_extra, 'N/A') as products_description_extra
from products p
LEFT OUTER JOIN products_description pd on p.products_id = pd.products_id
LEFT OUTER JOIN products_description_ncbi_sp pdns on p.products_id = pdns.products_id
LEFT OUTER JOIN products_extra pe on p.products_id = pe.products_id
where p.products_id = '29913' and pd.language_id = 1
SELECT `options_values_price` as `price`, `products_options_values_name` as `package`
FROM `products_attributes`
JOIN `products_options_values` ON `products_options_values`.`products_options_values_id` = `products_attributes`.`options_values_id`
WHERE `products_attributes`.`products_id` = '29913'
⇄⧉testing_protocols => string (1843) "FCM (Flow Cytometry)||Flow cytometric analysis of Hela cells with BMI1 antib...
$value['testing_protocols']
FCM (Flow Cytometry)||Flow cytometric analysis of Hela cells with BMI1 antibody at 1/100 dilution (blue) compared with an unlabelled control (cells without incubation with primary antibody; red). Goat anti mouse IgG (FITC) was used as the secondary antibody.||AAA29913_FCM8.jpg!!ICC (Immunocytochemistry)||ICC staining Bmi1 in Hela cells (red). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA29913_ICC7.jpg!!ICC (Immunocytochemistry)||ICC staining Bmi1 in Lovo cells (red). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA29913_ICC6.jpg!!ICC (Immunocytochemistry)||ICC staining Bmi1 in A549 cells (red). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA29913_ICC5.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded human breast cancer tissue using anti-BMI1 antibody. Counter stained with hematoxylin.||AAA29913_IHC4.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded human colon cancer tissue using anti-Bmi1 antibody. Counter stained with hematoxylin.||AAA29913_IHC3.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded human tonsil tissue using anti-Bmi1 antibody. Counter stained with hematoxylin.||AAA29913_IHC2.jpg!!WB (Western Blot)||Western blot analysis of Bmi1 on different lysates using anti-Bmi1 antibody at 1/1, 000 dilution. Positive control: Lane 1: 293T Lane 2: Jurkat Lane 3: Hela Lane 4: MCF-7 Lane 5: HepG2 Lane 6: NIH/3T3 Lane 7: PC12 Lane 8: Mouse kidney Lane 9: Human kidney Lane 10: K562 Lane 11: Human brain||AAA29913_WB.jpg
⇄etc_term1 => string (63) "Immunogen||Recombinant protein within human Bmi1 full sequence."
⇄⧉products_name_syn => string (653) "B lymphoma Mo MLV insertion region (mouse) antibody; B lymphoma Mo MLV inser...
$value['products_name_syn']
B lymphoma Mo MLV insertion region (mouse) antibody; B lymphoma Mo MLV insertion region 1 homolog antibody; Bmi 1 antibody; BMI1 antibody; BMI1 polycomb ring finger oncogene antibody; BMI1_HUMAN antibody; Flvi 2/bmi 1 antibody; FLVI2/BMI1 antibody; MGC12685 antibody; Murine leukemia viral (bmi 1) oncogene homolog antibody; Oncogene BMI 1 antibody; PCGF 4 antibody; PCGF4 antibody; Polycomb complex protein BMI 1 antibody; Polycomb complex protein BMI-1 antibody; Polycomb group protein Bmi1 antibody; Polycomb group ring finger 4 antibody; Polycomb group RING finger protein 4 antibody; RING finger protein 51 antibody; RNF 51 antibody; RNF51 antibody
⇄products_gene_name => string (4) "BMI1"
$value['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value['products_gene_name_syn']
⇄⧉products_description => string (348) "The Bmi-1 was identified initially as an oncogene that cooperates with c-myc...
$value['products_description']
The Bmi-1 was identified initially as an oncogene that cooperates with c-myc in the generation of B-cell lymphoma. It contributes to the maintenance of cell identity, stem cell self-renewal, cell cycle regulation, and oncogenesis by maintaining the silenced state of genes that promote cell lineage specification, cell death, and cell-cycle arrest.
⇄products_references => string (3) "N/A"
$value['products_references']
⇄products_related_diseases => string (3) "N/A"
$value['products_related_diseases']
⇄products_categories => string (16) "Total protein Ab"
$value['products_categories']
⇄products_search_terms => string (3) "N/A"
$value['products_search_terms']
⇄ncbi_full_name => string (30) "polycomb complex protein BMI-1"
$value['ncbi_full_name']
⇄ncbi_full_name_syn => string (41) "BMI1 proto-oncogene, polycomb ring finger"
⇄⧉ncbi_protein_info => string (255) "polycomb complex protein BMI-1; flvi-2/bmi-1; ring finger protein 51; polyco...
$value['ncbi_protein_info']
polycomb complex protein BMI-1; flvi-2/bmi-1; ring finger protein 51; polycomb group protein Bmi1; BMI1 polycomb ring finger oncogene; polycomb group RING finger protein 4; BMI1 polycomb ring finger proto-oncogene; B lymphoma Mo-MLV insertion region 1 hom
Cellular Senescence Pathway||905991!!Cellular Responses To Stress Pathway||645258!!MicroRNAs In Cancer Pathway||852705!!MicroRNAs In Cancer Pathway||852928!!Oxidative Stress Induced Senescence Pathway||905993!!Senescence And Autophagy Pathway||198780!!Transcriptional Misregulation In Cancer Pathway||523016!!Transcriptional Misregulation In Cancer Pathway||522987!!Validated Targets Of C-MYC Transcriptional Activation Pathway||169351
⇄sp_protein_name => string (30) "Polycomb complex protein BMI-1"
$value['sp_protein_name']
⇄sp_protein_name_syn => string (60) "Polycomb group RING finger protein 4; RING finger protein 51"
⇄⧉testing_protocols => string (1843) "FCM (Flow Cytometry)||Flow cytometric analysis of Hela cells with BMI1 antib...
$value->a['testing_protocols']
FCM (Flow Cytometry)||Flow cytometric analysis of Hela cells with BMI1 antibody at 1/100 dilution (blue) compared with an unlabelled control (cells without incubation with primary antibody; red). Goat anti mouse IgG (FITC) was used as the secondary antibody.||AAA29913_FCM8.jpg!!ICC (Immunocytochemistry)||ICC staining Bmi1 in Hela cells (red). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA29913_ICC7.jpg!!ICC (Immunocytochemistry)||ICC staining Bmi1 in Lovo cells (red). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA29913_ICC6.jpg!!ICC (Immunocytochemistry)||ICC staining Bmi1 in A549 cells (red). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA29913_ICC5.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded human breast cancer tissue using anti-BMI1 antibody. Counter stained with hematoxylin.||AAA29913_IHC4.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded human colon cancer tissue using anti-Bmi1 antibody. Counter stained with hematoxylin.||AAA29913_IHC3.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded human tonsil tissue using anti-Bmi1 antibody. Counter stained with hematoxylin.||AAA29913_IHC2.jpg!!WB (Western Blot)||Western blot analysis of Bmi1 on different lysates using anti-Bmi1 antibody at 1/1, 000 dilution. Positive control: Lane 1: 293T Lane 2: Jurkat Lane 3: Hela Lane 4: MCF-7 Lane 5: HepG2 Lane 6: NIH/3T3 Lane 7: PC12 Lane 8: Mouse kidney Lane 9: Human kidney Lane 10: K562 Lane 11: Human brain||AAA29913_WB.jpg
⇄etc_term1 => string (63) "Immunogen||Recombinant protein within human Bmi1 full sequence."
⇄⧉products_name_syn => string (653) "B lymphoma Mo MLV insertion region (mouse) antibody; B lymphoma Mo MLV inser...
$value->a['products_name_syn']
B lymphoma Mo MLV insertion region (mouse) antibody; B lymphoma Mo MLV insertion region 1 homolog antibody; Bmi 1 antibody; BMI1 antibody; BMI1 polycomb ring finger oncogene antibody; BMI1_HUMAN antibody; Flvi 2/bmi 1 antibody; FLVI2/BMI1 antibody; MGC12685 antibody; Murine leukemia viral (bmi 1) oncogene homolog antibody; Oncogene BMI 1 antibody; PCGF 4 antibody; PCGF4 antibody; Polycomb complex protein BMI 1 antibody; Polycomb complex protein BMI-1 antibody; Polycomb group protein Bmi1 antibody; Polycomb group ring finger 4 antibody; Polycomb group RING finger protein 4 antibody; RING finger protein 51 antibody; RNF 51 antibody; RNF51 antibody
⇄products_gene_name => string (4) "BMI1"
$value->a['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value->a['products_gene_name_syn']
⇄⧉products_description => string (348) "The Bmi-1 was identified initially as an oncogene that cooperates with c-myc...
$value->a['products_description']
The Bmi-1 was identified initially as an oncogene that cooperates with c-myc in the generation of B-cell lymphoma. It contributes to the maintenance of cell identity, stem cell self-renewal, cell cycle regulation, and oncogenesis by maintaining the silenced state of genes that promote cell lineage specification, cell death, and cell-cycle arrest.
⇄products_references => string (3) "N/A"
$value->a['products_references']
⇄products_related_diseases => string (3) "N/A"
$value->a['products_related_diseases']
⇄products_categories => string (16) "Total protein Ab"
$value->a['products_categories']
⇄products_search_terms => string (3) "N/A"
$value->a['products_search_terms']
⇄ncbi_full_name => string (30) "polycomb complex protein BMI-1"
$value->a['ncbi_full_name']
⇄ncbi_full_name_syn => string (41) "BMI1 proto-oncogene, polycomb ring finger"
⇄⧉ncbi_protein_info => string (255) "polycomb complex protein BMI-1; flvi-2/bmi-1; ring finger protein 51; polyco...
$value->a['ncbi_protein_info']
polycomb complex protein BMI-1; flvi-2/bmi-1; ring finger protein 51; polycomb group protein Bmi1; BMI1 polycomb ring finger oncogene; polycomb group RING finger protein 4; BMI1 polycomb ring finger proto-oncogene; B lymphoma Mo-MLV insertion region 1 hom
Cellular Senescence Pathway||905991!!Cellular Responses To Stress Pathway||645258!!MicroRNAs In Cancer Pathway||852705!!MicroRNAs In Cancer Pathway||852928!!Oxidative Stress Induced Senescence Pathway||905993!!Senescence And Autophagy Pathway||198780!!Transcriptional Misregulation In Cancer Pathway||523016!!Transcriptional Misregulation In Cancer Pathway||522987!!Validated Targets Of C-MYC Transcriptional Activation Pathway||169351
⇄sp_protein_name => string (30) "Polycomb complex protein BMI-1"
$value->a['sp_protein_name']
⇄sp_protein_name_syn => string (60) "Polycomb group RING finger protein 4; RING finger protein 51"
⇄⧉testing_protocols => string (1843) "FCM (Flow Cytometry)||Flow cytometric analysis of Hela cells with BMI1 antib...
$value->d['testing_protocols']
FCM (Flow Cytometry)||Flow cytometric analysis of Hela cells with BMI1 antibody at 1/100 dilution (blue) compared with an unlabelled control (cells without incubation with primary antibody; red). Goat anti mouse IgG (FITC) was used as the secondary antibody.||AAA29913_FCM8.jpg!!ICC (Immunocytochemistry)||ICC staining Bmi1 in Hela cells (red). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA29913_ICC7.jpg!!ICC (Immunocytochemistry)||ICC staining Bmi1 in Lovo cells (red). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA29913_ICC6.jpg!!ICC (Immunocytochemistry)||ICC staining Bmi1 in A549 cells (red). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA29913_ICC5.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded human breast cancer tissue using anti-BMI1 antibody. Counter stained with hematoxylin.||AAA29913_IHC4.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded human colon cancer tissue using anti-Bmi1 antibody. Counter stained with hematoxylin.||AAA29913_IHC3.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded human tonsil tissue using anti-Bmi1 antibody. Counter stained with hematoxylin.||AAA29913_IHC2.jpg!!WB (Western Blot)||Western blot analysis of Bmi1 on different lysates using anti-Bmi1 antibody at 1/1, 000 dilution. Positive control: Lane 1: 293T Lane 2: Jurkat Lane 3: Hela Lane 4: MCF-7 Lane 5: HepG2 Lane 6: NIH/3T3 Lane 7: PC12 Lane 8: Mouse kidney Lane 9: Human kidney Lane 10: K562 Lane 11: Human brain||AAA29913_WB.jpg
⇄etc_term1 => string (63) "Immunogen||Recombinant protein within human Bmi1 full sequence."
⇄⧉products_name_syn => string (653) "B lymphoma Mo MLV insertion region (mouse) antibody; B lymphoma Mo MLV inser...
$value->d['products_name_syn']
B lymphoma Mo MLV insertion region (mouse) antibody; B lymphoma Mo MLV insertion region 1 homolog antibody; Bmi 1 antibody; BMI1 antibody; BMI1 polycomb ring finger oncogene antibody; BMI1_HUMAN antibody; Flvi 2/bmi 1 antibody; FLVI2/BMI1 antibody; MGC12685 antibody; Murine leukemia viral (bmi 1) oncogene homolog antibody; Oncogene BMI 1 antibody; PCGF 4 antibody; PCGF4 antibody; Polycomb complex protein BMI 1 antibody; Polycomb complex protein BMI-1 antibody; Polycomb group protein Bmi1 antibody; Polycomb group ring finger 4 antibody; Polycomb group RING finger protein 4 antibody; RING finger protein 51 antibody; RNF 51 antibody; RNF51 antibody
⇄products_gene_name => string (4) "BMI1"
$value->d['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value->d['products_gene_name_syn']
⇄⧉products_description => string (348) "The Bmi-1 was identified initially as an oncogene that cooperates with c-myc...
$value->d['products_description']
The Bmi-1 was identified initially as an oncogene that cooperates with c-myc in the generation of B-cell lymphoma. It contributes to the maintenance of cell identity, stem cell self-renewal, cell cycle regulation, and oncogenesis by maintaining the silenced state of genes that promote cell lineage specification, cell death, and cell-cycle arrest.
⇄products_references => string (3) "N/A"
$value->d['products_references']
⇄products_related_diseases => string (3) "N/A"
$value->d['products_related_diseases']
⇄products_categories => string (16) "Total protein Ab"
$value->d['products_categories']
⇄products_search_terms => string (3) "N/A"
$value->d['products_search_terms']
⇄ncbi_full_name => string (30) "polycomb complex protein BMI-1"
$value->d['ncbi_full_name']
⇄ncbi_full_name_syn => string (41) "BMI1 proto-oncogene, polycomb ring finger"
⇄⧉ncbi_protein_info => string (255) "polycomb complex protein BMI-1; flvi-2/bmi-1; ring finger protein 51; polyco...
$value->d['ncbi_protein_info']
polycomb complex protein BMI-1; flvi-2/bmi-1; ring finger protein 51; polycomb group protein Bmi1; BMI1 polycomb ring finger oncogene; polycomb group RING finger protein 4; BMI1 polycomb ring finger proto-oncogene; B lymphoma Mo-MLV insertion region 1 hom
Cellular Senescence Pathway||905991!!Cellular Responses To Stress Pathway||645258!!MicroRNAs In Cancer Pathway||852705!!MicroRNAs In Cancer Pathway||852928!!Oxidative Stress Induced Senescence Pathway||905993!!Senescence And Autophagy Pathway||198780!!Transcriptional Misregulation In Cancer Pathway||523016!!Transcriptional Misregulation In Cancer Pathway||522987!!Validated Targets Of C-MYC Transcriptional Activation Pathway||169351
⇄sp_protein_name => string (30) "Polycomb complex protein BMI-1"
$value->d['sp_protein_name']
⇄sp_protein_name_syn => string (60) "Polycomb group RING finger protein 4; RING finger protein 51"
⇄⧉testing_protocols => string (1843) "FCM (Flow Cytometry)||Flow cytometric analysis of Hela cells with BMI1 antib...
$value[0]['_source']['testing_protocols']
FCM (Flow Cytometry)||Flow cytometric analysis of Hela cells with BMI1 antibody at 1/100 dilution (blue) compared with an unlabelled control (cells without incubation with primary antibody; red). Goat anti mouse IgG (FITC) was used as the secondary antibody.||AAA29913_FCM8.jpg!!ICC (Immunocytochemistry)||ICC staining Bmi1 in Hela cells (red). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA29913_ICC7.jpg!!ICC (Immunocytochemistry)||ICC staining Bmi1 in Lovo cells (red). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA29913_ICC6.jpg!!ICC (Immunocytochemistry)||ICC staining Bmi1 in A549 cells (red). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA29913_ICC5.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded human breast cancer tissue using anti-BMI1 antibody. Counter stained with hematoxylin.||AAA29913_IHC4.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded human colon cancer tissue using anti-Bmi1 antibody. Counter stained with hematoxylin.||AAA29913_IHC3.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded human tonsil tissue using anti-Bmi1 antibody. Counter stained with hematoxylin.||AAA29913_IHC2.jpg!!WB (Western Blot)||Western blot analysis of Bmi1 on different lysates using anti-Bmi1 antibody at 1/1, 000 dilution. Positive control: Lane 1: 293T Lane 2: Jurkat Lane 3: Hela Lane 4: MCF-7 Lane 5: HepG2 Lane 6: NIH/3T3 Lane 7: PC12 Lane 8: Mouse kidney Lane 9: Human kidney Lane 10: K562 Lane 11: Human brain||AAA29913_WB.jpg
⇄etc_term1 => string (63) "Immunogen||Recombinant protein within human Bmi1 full sequence."
⇄⧉products_name_syn => string (653) "B lymphoma Mo MLV insertion region (mouse) antibody; B lymphoma Mo MLV inser...
$value[0]['_source']['products_name_syn']
B lymphoma Mo MLV insertion region (mouse) antibody; B lymphoma Mo MLV insertion region 1 homolog antibody; Bmi 1 antibody; BMI1 antibody; BMI1 polycomb ring finger oncogene antibody; BMI1_HUMAN antibody; Flvi 2/bmi 1 antibody; FLVI2/BMI1 antibody; MGC12685 antibody; Murine leukemia viral (bmi 1) oncogene homolog antibody; Oncogene BMI 1 antibody; PCGF 4 antibody; PCGF4 antibody; Polycomb complex protein BMI 1 antibody; Polycomb complex protein BMI-1 antibody; Polycomb group protein Bmi1 antibody; Polycomb group ring finger 4 antibody; Polycomb group RING finger protein 4 antibody; RING finger protein 51 antibody; RNF 51 antibody; RNF51 antibody
⇄products_gene_name => string (4) "BMI1"
$value[0]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[0]['_source']['products_gene_name_syn']
⇄⧉products_description => string (348) "The Bmi-1 was identified initially as an oncogene that cooperates with c-myc...
$value[0]['_source']['products_description']
The Bmi-1 was identified initially as an oncogene that cooperates with c-myc in the generation of B-cell lymphoma. It contributes to the maintenance of cell identity, stem cell self-renewal, cell cycle regulation, and oncogenesis by maintaining the silenced state of genes that promote cell lineage specification, cell death, and cell-cycle arrest.
⇄products_references => string (3) "N/A"
$value[0]['_source']['products_references']
⇄products_related_diseases => string (3) "N/A"
$value[0]['_source']['products_related_diseases']
⇄products_categories => string (16) "Total protein Ab"
$value[0]['_source']['products_categories']
⇄ncbi_full_name => string (30) "polycomb complex protein BMI-1"
$value[0]['_source']['ncbi_full_name']
⇄ncbi_full_name_syn => string (41) "BMI1 proto-oncogene, polycomb ring finger"
⇄⧉ncbi_protein_info => string (255) "polycomb complex protein BMI-1; flvi-2/bmi-1; ring finger protein 51; polyco...
$value[0]['_source']['ncbi_protein_info']
polycomb complex protein BMI-1; flvi-2/bmi-1; ring finger protein 51; polycomb group protein Bmi1; BMI1 polycomb ring finger oncogene; polycomb group RING finger protein 4; BMI1 polycomb ring finger proto-oncogene; B lymphoma Mo-MLV insertion region 1 hom
Cellular Senescence Pathway||905991!!Cellular Responses To Stress Pathway||645258!!MicroRNAs In Cancer Pathway||852705!!MicroRNAs In Cancer Pathway||852928!!Oxidative Stress Induced Senescence Pathway||905993!!Senescence And Autophagy Pathway||198780!!Transcriptional Misregulation In Cancer Pathway||523016!!Transcriptional Misregulation In Cancer Pathway||522987!!Validated Targets Of C-MYC Transcriptional Activation Pathway||169351
⇄sp_protein_name => string (30) "Polycomb complex protein BMI-1"
$value[0]['_source']['sp_protein_name']
⇄sp_protein_name_syn => string (60) "Polycomb group RING finger protein 4; RING finger protein 51"
⇄⧉search_terms => string (1293) "aaa29913 mouse human rat monoclonal b3 g5 proa affinity purified 1*tbs ph7.4...
$value[0]['_source']['search_terms']
aaa29913 mouse human rat monoclonal b3 g5 proa affinity purified 1*tbs ph7.4 1 bsa 40 glycerol preservative 0.05 sodium azide western blot wb immunocytochemistry icc immunohistochemistry ihc flow cytometry fc facs 1:1000 1:200 1:100 analysis of bmi1 on different lysates using anti antibody at 000 dilution positive control   lane 293t 2 jurkat 3 hela  4 mcf 7 5 hepg2  6 nih 3t3 pc12 8 kidney 9 10 k562 11 brain aaa29913_wb immunohistochemical paraffin embedded tonsil tissue counter stained with hematoxylin aaa29913_ihc2 colon cancer aaa29913_ihc3 breast aaa29913_ihc4 staining in a549 cells red were fixed paraformaldehyde permeabilised 0.25 triton x100 pbs aaa29913_icc5 lovo aaa29913_icc6 hela aaa29913_icc7 cytometric 100 blue compared an unlabelled without incubation primary goat igg fitc was used as the secondary aaa29913_fc8 b lymphoma mo mlv insertion region homolog bmi polycomb ring finger oncogene bmi1_human flvi flvi2 mgc12685 murine leukemia viral pcgf pcgf4 complex protein group 51 rnf rnf51 proto hom 36,949 da 27883842 np_005171.4 p35226 nm_005180.8 q16030 q5t8z3 q96f37 164831 total ab immunogen recombinant within full sequence conjugation unconjugated ph7.41 bsa40 at000 293t2 jurkat3 hela 4 mcf7 hepg2 6 pc128 kidney9 k56211 cytometric100 group51
WB: 1:1000<br>IP: 6 ul/mg lysate<br>IHC: 1:100 to 1:500. Epitope retrieval with citrate buffer pH6.0 is recommended for FFPE tissue sections.<br>ICC: 1:100 to 1:500. Epitope retrieval with citrate buffer pH6.0 is recommended for FFPE cell sections.<br>FC/FACS: Fixed in 4% formaldehyde and permeabilized with 90% methanol. 0.5 ul per 1 x 10^6 cells.
⇄⧉testing_protocols => string (3032) "WB (Western Blot)||<b>Detection of human BMI1 by western blot.</b> <i>Sample...
$value[1]['_source']['testing_protocols']
WB (Western Blot)||<b>Detection of human BMI1 by western blot.</b> <i>Samples:</i> Whole cell lysate (10 ug) from MOLT-4, HeLa, HEK293T, Jurkat, LNCaP, RKO, Hep-G2, and U2OS cells prepared using NETN lysis buffer.</b> <i>Antibody:</i> Rabbit anti-BMI1 recombinant monoclonal antibody (AAA23838 lot 1) used at 1:1000. <i>Secondary:</i> HRP-conjugated goat anti-rabbit IgG . <i>Detection:</i> Chemiluminescence with an exposure time of 10 seconds. Lower Panel: Rabbit anti-COPB2 antibody .||AAA23838_WB8.jpg!!WB (Western Blot)||<b>Detection of mouse BMI1 by western blot.</b> <i>Samples:</i> Whole cell lysate (10 ug) from mIMCD-3, A20, NIH 3T3, CT26, EL4, RenCa, and CH27 cells prepared using NETN lysis buffer. <i>Antibody:</i> Rabbit anti-BMI1 recombinant monoclonal antibody (AAA23838 lot 1) used at 1:1000. <i>Secondary:</i> HRP-conjugated goat anti-rabbit IgG . <i>Detection:</i> Chemiluminescence with an exposure time of 30 seconds. Lower Panel: Rabbit anti-COPB2 antibody .||AAA23838_WB7.jpg!!IP (Immunoprecipitation)||<b>Detection of human BMI1 by western blot of immunoprecipitates.</b> <i>Samples:</i> Whole cell lysate (1.0 mg per IP reaction; 20% of IP loaded) from HEK293T cells prepared using NETN lysis buffer. <i>Antibodies:</i> Rabbit anti-BMI1 recombinant monoclonal antibody (AAA23838 lot 1) used for IP at 6 ul/mg lysate. BMI1 was also immunoprecipitated by rabbit anti-BMI1 antibodies and BL1683A-4F6. For blotting immunoprecipitated BMI1, AAA23838 was used at 1:1000. <i>Detection:</i> Chemiluminescence with an exposure time of 10 seconds.||AAA23838_IP6.jpg!!IHC (Immunohistochemistry)||<b>Detection of human BMI1 in FFPE prostate carcinoma by immunohistochemistry.</b> <i>Antibody:</i> Rabbit anti-BMI1 recombinant monoclonal antibody (AAA23838 lot 1). <i>Secondary:</I> HRP-conjugated goat anti-rabbit IgG . <i>Substrate:</i> DAB.||AAA23838_IHC5.jpg!!IHC (Immunohistochemistry)||<b>Detection of mouse BMI1 in FFPE renal cell carcinoma by immunohistochemistry.</b> <i>Antibody:</i> Rabbit anti-BMI1 recombinant monoclonal antibody (AAA23838 lot 1). <i>Secondary:</I> HRP-conjugated goat anti-rabbit IgG . <i>Substrate:</i> DAB.||AAA23838_IHC4.jpg!!ICC (Immunocytochemistry)||<b>Detection of human BMI1 in FFPE LNCaP cells by immunocytochemistry.</b> <i>Antibody:</i> Rabbit anti-BMI1 recombinant monoclonal antibody (AAA23838 lot 1). <i>Secondary:</I> HRP-conjugated goat anti-rabbit IgG . <i>Substrate:</i> DAB.||AAA23838_ICC3.jpg!!FCM (Flow Cytometry)||<b>Detection of mouse BMI1 (shaded) in NIH3T3 cells by flow cytometry.</b> <i>Antibody:</i> Rabbit anti-BMI1 recombinant monoclonal antibody (AAA23838) or isotype control (unshaded). <i>Secondary:</i> DyLight 650-conjugated goat anti-rabbit IgG .||AAA23838_FCM2.jpg!!FCM (Flow Cytometry)||<b>Detection of human BMI1 (shaded) in Jurkat cells by flow cytometry.</b> <i>Antibody:</i> Rabbit anti-BMI1 recombinant monoclonal antibody (AAA23838) or isotype control (unshaded). <i>Secondary:</i> DyLight 650-conjugated goat anti-rabbit IgG .||AAA23838_FCM.jpg
⇄etc_term1 => string (64) "Immunogen||Between 623 and C-terminus!!Conjugation||Unconjugated"
⇄⧉products_name_syn => string (408) "polycomb complex protein BMI-1; flvi-2/bmi-1; RNF51; ring finger protein 51;...
$value[1]['_source']['products_name_syn']
polycomb complex protein BMI-1; flvi-2/bmi-1; RNF51; ring finger protein 51; polycomb group RING finger protein 4; polycomb group protein Bmi1; murine leukemia viral (bmi-1) oncogene homolog; B lymphoma Mo-MLV insertion region 1 homolog; FLVI2/BMI1; BMI1 polycomb ring finger proto-oncogene; BMI1 polycomb ring finger oncogene; PCGF4; Polycomb complex protein BMI-1; BMI1 proto-oncogene, polycomb ring finger
⇄products_gene_name => string (4) "BMI1"
$value[1]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[1]['_source']['products_gene_name_syn']
⇄⧉products_description => string (486) "BMI1 (B lymphoma Mo-MLV insertion region 1 homolog) is a core component of t...
$value[1]['_source']['products_description']
BMI1 (B lymphoma Mo-MLV insertion region 1 homolog) is a core component of the polycomb group (PcG) multiprotein PRC1 complex which plays an important role in transcriptional repression of gene expression during development. BMI1 association with RING protein 1B is important to the E3 ligase activity of RING1B in the PRC1 complex. BMI1 is an oncogene whose overexpression is associated with many types of human tumors and is a stem-cell marker and regulator of stem cell self-renewal.
⇄⧉ncbi_protein_info => string (255) "polycomb complex protein BMI-1; flvi-2/bmi-1; ring finger protein 51; polyco...
$value[1]['_source']['ncbi_protein_info']
polycomb complex protein BMI-1; flvi-2/bmi-1; ring finger protein 51; polycomb group protein Bmi1; BMI1 polycomb ring finger oncogene; polycomb group RING finger protein 4; BMI1 polycomb ring finger proto-oncogene; B lymphoma Mo-MLV insertion region 1 hom
Cellular Senescence Pathway||905991!!Cellular Responses To Stress Pathway||645258!!MicroRNAs In Cancer Pathway||852705!!MicroRNAs In Cancer Pathway||852928!!Oxidative Stress Induced Senescence Pathway||905993!!Senescence And Autophagy Pathway||198780!!Transcriptional Misregulation In Cancer Pathway||523016!!Transcriptional Misregulation In Cancer Pathway||522987!!Validated Targets Of C-MYC Transcriptional Activation Pathway||169351
⇄sp_protein_name => string (30) "Polycomb complex protein BMI-1"
$value[1]['_source']['sp_protein_name']
⇄sp_protein_name_syn => string (60) "Polycomb group RING finger protein 4; RING finger protein 51"
⇄⧉testing_protocols => string (1541) "ICC (Immunocytochemistry)||ICC staining Bmi1 in SW480 cells (green). The nuc...
$value[2]['_source']['testing_protocols']
ICC (Immunocytochemistry)||ICC staining Bmi1 in SW480 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA30255_ICC8.jpg!!ICC (Immunocytochemistry)||ICC staining Bmi1 in A549 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA30255_ICC7.jpg!!ICC (Immunocytochemistry)||ICC staining Bmi1 in Hela cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA30255_ICC6.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded human lung cancer tissue using anti-Bmi1 antibody. Counter stained with hematoxylin.||AAA30255_IHC5.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded rat smooth muscle tissue using anti-Bmi1 antibody. Counter stained with hematoxylin.||AAA30255_IHC4.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue using anti-Bmi1 antibody. Counter stained with hematoxylin.||AAA30255_IHC3.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded human tonsil tissue using anti-Bmi1 antibody. Counter stained with hematoxylin.||AAA30255_IHC2.jpg!!WB (Western Blot)||Western blot analysis of Bmi1 on different lysates using anti-Bmi1 antibody at 1/1, 000 dilution. Positive control: Lane 1: K562 Lane 2: PC-12||AAA30255_WB.jpg
⇄⧉products_name_syn => string (653) "B lymphoma Mo MLV insertion region (mouse) antibody; B lymphoma Mo MLV inser...
$value[2]['_source']['products_name_syn']
B lymphoma Mo MLV insertion region (mouse) antibody; B lymphoma Mo MLV insertion region 1 homolog antibody; Bmi 1 antibody; BMI1 antibody; BMI1 polycomb ring finger oncogene antibody; BMI1_HUMAN antibody; Flvi 2/bmi 1 antibody; FLVI2/BMI1 antibody; MGC12685 antibody; Murine leukemia viral (bmi 1) oncogene homolog antibody; Oncogene BMI 1 antibody; PCGF 4 antibody; PCGF4 antibody; Polycomb complex protein BMI 1 antibody; Polycomb complex protein BMI-1 antibody; Polycomb group protein Bmi1 antibody; Polycomb group ring finger 4 antibody; Polycomb group RING finger protein 4 antibody; RING finger protein 51 antibody; RNF 51 antibody; RNF51 antibody
⇄products_gene_name => string (4) "BMI1"
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⇄products_gene_name_syn => string (3) "N/A"
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⇄⧉products_description => string (1145) "In Drosophila, Polycomb (Pc-g) gene family encodes chromatin proteins that a...
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In Drosophila, Polycomb (Pc-g) gene family encodes chromatin proteins that are required for the repression of homeotic loci in embryonic development. Mel-18 and Bmi-1, mammalian homologs of Drosophila Pc-g group proteins, are similarly expressed during development and implicated in the regulation of gene expression, axial skeleton development, control of proliferation and survival of haematopoietic cells. Mel-18 directly binds to DNA through a RING-finger motif and preferentially associates with juxtaposed enhancer elements on various genes, including Bcl-2, c-Myc and Hox. Mel-18 is an immediate early response gene within the c-Myc/Cdc25 signaling cascade that exhibits tumor suppressor activity and negatively regulates cell cycle progression by blocking S phase entry. Alternatively, Bmi-1 has been identified as a potent oncogene as it contributes to the transcriptional activation of genes implicated in early lymphoid development. Proviral activation of Bmi-1 expression corresponds to enhanced gene-specific activation of other proto-oncogenes, including c-Myc and Pim, subsequently resulting in the progression of lymphomagenesis.
⇄products_references => string (3) "N/A"
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⇄products_related_diseases => string (3) "N/A"
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⇄products_categories => string (16) "Total protein Ab"
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⇄ncbi_full_name => string (30) "polycomb complex protein BMI-1"
$value[2]['_source']['ncbi_full_name']
⇄ncbi_full_name_syn => string (41) "BMI1 proto-oncogene, polycomb ring finger"
⇄⧉ncbi_protein_info => string (255) "polycomb complex protein BMI-1; flvi-2/bmi-1; ring finger protein 51; polyco...
$value[2]['_source']['ncbi_protein_info']
polycomb complex protein BMI-1; flvi-2/bmi-1; ring finger protein 51; polycomb group protein Bmi1; BMI1 polycomb ring finger oncogene; polycomb group RING finger protein 4; BMI1 polycomb ring finger proto-oncogene; B lymphoma Mo-MLV insertion region 1 hom
Cellular Senescence Pathway||905991!!Cellular Responses To Stress Pathway||645258!!MicroRNAs In Cancer Pathway||852705!!MicroRNAs In Cancer Pathway||852928!!Oxidative Stress Induced Senescence Pathway||905993!!Senescence And Autophagy Pathway||198780!!Transcriptional Misregulation In Cancer Pathway||523016!!Transcriptional Misregulation In Cancer Pathway||522987!!Validated Targets Of C-MYC Transcriptional Activation Pathway||169351
⇄sp_protein_name => string (30) "Polycomb complex protein BMI-1"
$value[2]['_source']['sp_protein_name']
⇄sp_protein_name_syn => string (60) "Polycomb group RING finger protein 4; RING finger protein 51"
⇄⧉search_terms => string (1099) "aaa30255 rabbit human rat monoclonal jj093 3 proa affinity purified 1*tbs ph...
$value[2]['_source']['search_terms']
aaa30255 rabbit human rat monoclonal jj093 3 proa affinity purified 1*tbs ph7.4 1 bsa 40 glycerol preservative 0.05 sodium azide western blot wb immunocytochemistry icc immunofluorescence if immunohistochemistry ihc 1:1000 1:2000 1:50 1:200 analysis of bmi1 on different lysates using anti antibody at 000 dilution positive control lane k562 2 pc 12 aaa30255_wb immunohistochemical paraffin embedded tonsil tissue counter stained with hematoxylin aaa30255_ihc2 breast carcinoma aaa30255_ihc3 smooth muscle aaa30255_ihc4 lung cancer aaa30255_ihc5 staining in hela cells green the nuclear stain is dapi blue were fixed paraformaldehyde permeabilised 0.25 triton x100 pbs aaa30255_icc6 a549 aaa30255_icc7 sw480 aaa30255_icc8 b lymphoma mo mlv insertion region mouse homolog bmi polycomb ring finger oncogene bmi1_human flvi flvi2 mgc12685 murine leukemia viral pcgf 4 pcgf4 complex protein group 51 rnf rnf51 proto hom 36,949 da 27883842 np_005171.4 p35226 nm_005180.8 q16030 q5t8z3 q96f37 164831 total ab type recombinant immunogen conjugation unconjugated jj0933 ph7.41 bsa40 at000 k5622 pc12 group51
⇄⧉specificity => string (373) "This assay has high sensitivity and excellent specificity for detection of s...
$value[3]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of sTM. No significant cross-reactivity or interference between sTM and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between sTM and all the analogues, therefore, cross reaction may still exist in some cases.
⇄purity => string (3) "N/A"
$value[3]['_source']['purity']
⇄form => string (3) "N/A"
$value[3]['_source']['form']
⇄concentration => string (3) "N/A"
$value[3]['_source']['concentration']
⇄storage_stability => string (35) "Store all reagents at 2-8 degree C."
⇄⧉products_description => string (1372) "Intended Uses: This sTM ELISA kit is a 1.5 hour solid-phase ELISA designed f...
$value[3]['_source']['products_description']
Intended Uses: This sTM ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Porcine sTM. This ELISA kit for research use only, not for therapeutic or test applications!<br><br>Principle of the Assay: sTM ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-sTM antibody and an sTM-HRP conjugate. The assay sample and buffer are incubated together with sTM-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the sTM concentration since sTM from samples and sTM-HRP conjugate compete for the anti-sTM antibody binding site. Since the number of sites is limited, as more sites are occupied by sTM from the sample, fewer sites are left to bind sTM-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The sTM concentration in each sample is interpolated from this standard curve.
⇄⧉search_terms => string (546) "aaa17221 porcine this assay has high sensitivity and excellent specificity f...
$value[3]['_source']['search_terms']
aaa17221 porcine this assay has high sensitivity and excellent specificity for detection of stm no significant cross reactivity or interference between analogues was observed note limited by current skills knowledge it is impossible us to complete the all therefore reaction may still exist in some cases typical testing data standard curve reference only aaa17221_sc elisa kit soluble thrombomodulin cardiovascular samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative competitive 1.0 ng ml competitive1.0
⇄⧉specificity => string (185) "This assay has high sensitivity and excellent specificity for detection of H...
$value[4]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of Human sCD163. No significant cross-reactivity or interference between Human sCD163 and analogues was observed.
⇄purity => string (3) "N/A"
$value[4]['_source']['purity']
⇄form => string (3) "N/A"
$value[4]['_source']['form']
⇄concentration => string (3) "N/A"
$value[4]['_source']['concentration']
⇄storage_stability => string (22) "Store at 2-8 degree C."
$value[4]['_source']['storage_stability']
⇄app_tested => string (3) "N/A"
$value[4]['_source']['app_tested']
⇄app_notes => string (3) "N/A"
$value[4]['_source']['app_notes']
⇄testing_protocols => string (3) "N/A"
$value[4]['_source']['testing_protocols']
⇄⧉etc_term1 => string (183) "Assay Type||Quantitative Sandwich!!Samples||Serum, plasma and other biologic...
$value[4]['_source']['etc_term1']
Assay Type||Quantitative Sandwich!!Samples||Serum, plasma and other biological fluids!!Detection Range||0.156 ng/mL - 10 ng/mL!!Sensitivity||0.078 ng/mL (mean of 6 independent assays)
⇄⧉etc_term2 => string (420) "Intra-assay Precision||Intra-assay Precision (Precision within an assay) Thr...
$value[4]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay) Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision. Intra-Assay: CV<8%!!Inter-assay Precision||Inter-assay Precision (Precision between assays) Three samples of known concentration were tested in forty separate assays to assess inter-assay precision. CV(%) = SD/meanX100. Inter-Assay: CV<12%
⇄⧉products_description => string (908) "Principle of the Assay: This assay employs a two-site sandwich ELISA to quan...
$value[4]['_source']['products_description']
Principle of the Assay: This assay employs a two-site sandwich ELISA to quantitate sCD163 in Human serum, plasma. An antibody specific for sCD163 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any sCD163 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for sCD163 is added to the wells. After washing, Streptavidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of sCD163 bound in the initial step. The color development is stopped and the intensity of the color is measured.<br><br>Intended Uses: For the quantitative detection of Human Soluble CD163 (sCD163) concentration in serum, plasma and other biological fluids.
⇄products_references => string (3) "N/A"
$value[4]['_source']['products_references']
⇄⧉products_related_diseases => string (192) "Inflammation||354!!Neoplasms||254!!Necrosis||157!!Nervous System Diseases||1...
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Inflammation||354!!Neoplasms||254!!Necrosis||157!!Nervous System Diseases||102!!Brain Diseases||63!!Fibrosis||55!!Lung Diseases||46!!Adenocarcinoma||39!!Heart Diseases||29!!Kidney Diseases||27
⇄products_categories => string (3) "N/A"
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⇄ncbi_full_name => string (62) "scavenger receptor cysteine-rich type 1 protein M130 isoform a"
⇄⧉search_terms => string (658) "aaa13266 human this assay has high sensitivity and excellent specificity for...
$value[4]['_source']['search_terms']
aaa13266 human this assay has high sensitivity and excellent specificity for detection of scd163 no significant cross reactivity or interference between analogues was observed elisa kit soluble cd163 m130 mm130 antigen|macrophage associated antigen scavenger receptor cysteine rich type 1 protein isoform a molecule scari1 124,958 da hemoglobin cd_antigen 344179110 np_004235.4 q86vb7 nm_004244.5 q07898 q07899 q07900 q07901 q2vlh7 c9jig2 z22968 mrna samples serum plasma other biological fluids quantitative sandwich range 0.156 ng ml 10 0.078 intra precision within an three known concentration were tested twenty times on one plate to assess cv type1 ml10
⇄⧉specificity => string (379) "This assay has high sensitivity and excellent specificity for detection of s...
$value[5]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of sCD36. No significant cross-reactivity or interference between sCD36 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between sCD36 and all the analogues, therefore, cross reaction may still exist in some cases.
⇄purity => string (3) "N/A"
$value[5]['_source']['purity']
⇄form => string (3) "N/A"
$value[5]['_source']['form']
⇄concentration => string (3) "N/A"
$value[5]['_source']['concentration']
⇄storage_stability => string (35) "Store all reagents at 2-8 degree C."
⇄⧉products_description => string (1395) "Intended Uses: This sCD36 ELISA kit is a 1.5 hour solid-phase ELISA designed...
$value[5]['_source']['products_description']
Intended Uses: This sCD36 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of HumansCD36. This ELISA kit for research use only, not for therapeutic or test applications!<br><br>Principle of the Assay: sCD36 ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-sCD36 antibody and an sCD36-HRP conjugate. The assay sample and buffer are incubated together with sCD36-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the sCD36 concentration since sCD36 from samples and sCD36-HRP conjugate compete for the anti-sCD36 antibody binding site. Since the number of sites is limited, as more sites are occupied by sCD36 from the sample, fewer sites are left to bind sCD36-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The sCD36 concentration in each sample is interpolated from this standard curve.
⇄products_references => string (3) "N/A"
$value[5]['_source']['products_references']
⇄products_related_diseases => string (3) "N/A"
$value[5]['_source']['products_related_diseases']
⇄products_categories => string (10) "Immunology"
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⇄ncbi_full_name => string (3) "N/A"
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⇄ncbi_full_name_syn => string (3) "N/A"
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⇄ncbi_symbol => string (3) "N/A"
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⇄ncbi_symbol_syn => string (3) "N/A"
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⇄ncbi_protein_info => string (3) "N/A"
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⇄ncbi_chrom_loc => string (3) "N/A"
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⇄ncbi_gene_id => string (3) "N/A"
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⇄ncbi_mol_weight => string (3) "N/A"
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⇄ncbi_pathways => string (3) "N/A"
$value[5]['_source']['ncbi_pathways']
⇄sp_protein_name => string (3) "N/A"
$value[5]['_source']['sp_protein_name']
⇄sp_protein_name_syn => string (3) "N/A"
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⇄sp_gene_name => string (3) "N/A"
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⇄sp_gene_name_syn => string (3) "N/A"
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⇄sp_entry_name => string (3) "N/A"
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⇄sp_mim => string (3) "N/A"
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⇄sp_interactions => string (3) "N/A"
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⇄products_url => string (3) "N/A"
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⇄products_viewed => string (1) "0"
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⇄⧉search_terms => string (532) "aaa17226 human this assay has high sensitivity and excellent specificity for...
$value[5]['_source']['search_terms']
aaa17226 human this assay has high sensitivity and excellent specificity for detection of scd36 no significant cross reactivity or interference between analogues was observed note limited by current skills knowledge it is impossible us to complete the all therefore reaction may still exist in some cases typical testing data standard curve reference only aaa17226_sc elisa kit soluble cd36 immunology samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative competitive 0.1 ng ml competitive0.1
⇄⧉storage_stability => string (149) "Store at 4 degree C and protected from light upon receipt. Kit has a storage...
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Store at 4 degree C and protected from light upon receipt. Kit has a storage time of est. 6 months from receipt.<br>Shipping: Gel pack with blue ice.
⇄app_tested => string (3) "N/A"
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⇄⧉app_notes => string (197) "The detection principle of Plant Soluble Sugar Colorimetric Assay Kit is ant...
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The detection principle of Plant Soluble Sugar Colorimetric Assay Kit is anthrone colorimetry. It can be used for the determination of soluble monosaccharides, oligosaccharides and polysaccharides.
⇄⧉products_description => string (684) "Principle of the Assay: Carbohydrates are one of the important components of...
$value[6]['_source']['products_description']
Principle of the Assay: Carbohydrates are one of the important components of plant bodies, and are also the main raw materials and storage materials for metabolism. Soluble sugars refer to the reducing monosaccharides in the sample, sucrose and maltose that can be hydrolyzed into reducing monosaccharides under the determination conditions of this method, and starch that can be partially hydrolyzed into glucose. The detection principle is anthrone colorimetry. It can be used for the determination of soluble monosaccharides, oligosaccharides and polysaccharides. It has the advantages of high sensitivity, simplicity and speed, and suitable for the determination of trace samples.
⇄⧉search_terms => string (314) "aaa31532 the detection principle of plant soluble sugar colorimetric assay k...
$value[6]['_source']['search_terms']
aaa31532 the detection principle of plant soluble sugar colorimetric assay kit is anthrone colorimetry it can be used for determination monosaccharides oligosaccharides and polysaccharides typical testing data standard curve reference only aaa31532_sc cell metabolism biochemical range 0.0125 0.5 mg ml sensitivity
⇄⧉products_description => string (827) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[7]['_source']['products_description']
Principle of the Assay: As mentioned above, this kit utilizes the Double Antibody Sandwich ELISA technique. The pre-coated antibody is an anti-Porcine sTM monoclonal antibody, while the detection antibody is a biotinylated polyclonal antibody. Samples and biotinylated antibodies are added into ELISA plate wells and washed out with PBS or TBS after their respective additions to the wells. Then Avidin-peroxidase conjugates are added to the wells in after. TMB substrate is used for coloration after the enzyme conjugate has already been thoroughly washed out of the wells by PBS or TBS. TMB reacts to form a blue product from the peroxidase activity, and finally turns to yellow after addition of the stop solution (Color Reagent C). The color intensity and quantity of target analyte in the sample are positively correlated.
⇄products_references => string (3) "N/A"
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⇄products_related_diseases => string (3) "N/A"
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⇄products_categories => string (3) "N/A"
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⇄ncbi_full_name => string (33) "Sequence 1 from patent US 8076298"
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⇄ncbi_full_name_syn => string (3) "N/A"
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⇄ncbi_symbol => string (3) "N/A"
$value[7]['_source']['ncbi_symbol']
⇄ncbi_symbol_syn => string (3) "N/A"
$value[7]['_source']['ncbi_symbol_syn']
⇄ncbi_protein_info => string (3) "N/A"
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⇄ncbi_chrom_loc => string (3) "N/A"
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aaa22392 porcine typical testing data standard curve for reference only aaa22392_sc elisa kit soluble thrombomodulin stm sequence 1 from patent us 8076298 363888076 aew42344.1 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 20 ng ml 0.312 sensitivity up to 0.06 intra precision <= 8 inter 12 sequence1 range20 <=8 inter12
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Principle of the Assay: As mentioned above, this kit utilizes the Double Antibody Sandwich ELISA technique. The pre-coated antibody is an anti-Human sTM monoclonal antibody, while the detection antibody is a biotinylated polyclonal antibody. Samples and biotinylated antibodies are added into ELISA plate wells and washed out with PBS or TBS after their respective additions to the wells. Then Avidin-peroxidase conjugates are added to the wells in after. TMB substrate is used for coloration after the enzyme conjugate has already been thoroughly washed out of the wells by PBS or TBS. TMB reacts to form a blue product from the peroxidase activity, and finally turns to yellow after addition of the stop solution (Color Reagent C). The color intensity and quantity of target analyte in the sample are positively correlated.
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aaa22390 human typical testing data standard curve for reference only aaa22390_sc elisa kit soluble thrombomodulin stm sequence 1 from patent us 8076298 363888076 aew42344.1 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 100 ng ml 1.56 sensitivity up to 0.5 intra precision <= 8 inter 12 sequence1 range100 to0.5 <=8 inter12
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Intra-assay Precision||Intra-Assay Precision (Precision within an assay) Three samples of known concentration were tested on one plate to assess intra-assay precision. Intra-Assay: CV<8%!!Inter-assay Precision||Inter-Assay Precision (Precision between assays) Three samples of known concentration were tested in separate assays to assess inter-assay precision. CV(%) = SD/mean x 100. Inter-Assay: CV<10%
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Intended Uses: This sandwich kit is for the accurate quantitative detection of human Free Soluble Rankl in serum, plasma, cell culture supernates, cell lysates, tissue homogenates.<br><br>Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (ELISA). The plate has been pre-coated with human Free Soluble Rankl antibody. Free Soluble Rankl present in the sample is added and binds to antibodies coated on the wells. And then biotinylated human Free Soluble Rankl Antibody is added and binds to Free Soluble Rankl in the sample. Then Streptavidin-HRP is added and binds to the Biotinylated Free Soluble Rankl antibody. After incubation unbound Streptavidin-HRP is washed away during a washing step. Substrate solution is then added and color develops in proportion to the amount of human Free Soluble Rankl. The reaction is terminated by addition of acidic stop solution and absorbance is measured at 450 nm.
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aaa11385 human typical testing data standard curve for reference only aaa11385_sc elisa kit free soluble rankl samples serum plasma cell culture supernates lysates tissue homogenates assay type quantitative sandwich detection range 0.5ng l 300ng sensitivity 0.28ng intra precision within an three of known concentration were tested on one plate to assess cv<8 inter between assays in separate cv = sd mean x 100 cv<10 x100
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Principle of the Assay: As mentioned above, this kit utilizes the Double Antibody Sandwich ELISA technique. The pre-coated antibody is an anti-Mouse sTM monoclonal antibody, while the detection antibody is a biotinylated polyclonal antibody. Samples and biotinylated antibodies are added into ELISA plate wells and washed out with PBS or TBS after their respective additions to the wells. Then Avidin-peroxidase conjugates are added to the wells in after. TMB substrate is used for coloration after the enzyme conjugate has already been thoroughly washed out of the wells by PBS or TBS. TMB reacts to form a blue product from the peroxidase activity, and finally turns to yellow after addition of the stop solution (Color Reagent C). The color intensity and quantity of target analyte in the sample are positively correlated.
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aaa22410 mouse typical testing data standard curve for reference only aaa22410_sc elisa kit soluble thrombomodulin stm sequence 1 from patent us 8076298 363888076 aew42344.1 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 100 ng ml 1.56 sensitivity up to 0.5 intra precision <= 8 inter 12 sequence1 range100 to0.5 <=8 inter12
⇄⧉etc_term1 => string (130) "Samples||Serum, plasma, Cell Culture Supernatants, body fluid and tissue hom...
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Samples||Serum, plasma, Cell Culture Supernatants, body fluid and tissue homogenate!!Assay Type||Sandwich!!Sensitivity||0.1 ng/mL.
⇄⧉etc_term2 => string (199) "Intended Uses||This sGP130 ELISA kit is a 1.5 hour solid-phase ELISA designe...
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Intended Uses||This sGP130 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Rat sGP130. This ELISA kit for research use only, not for therapeutic applications!
⇄⧉products_description => string (1307) "<b>Principle of the assay: </b>sGP130 ELISA kit applies the quantitative san...
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<b>Principle of the assay: </b>sGP130 ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for sGP130. Standards or samples are then added to the microtiter plate wells and sGP130 if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of sGP130 present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for sGP130 are added to each well to "sandwich" the sGP130 immobilized on the plate. The microtiter plate undergoes incubation, and then the wells are thoroughly washed to remove all unbound components. Next, substrate solutions are added to each well. The enzyme (HRP) and substrate are allowed to react over a short incubation period. Only those wells that contain sGP130 and enzyme-conjugated antibody will exhibit a change in color. The enzyme-substrate reaction is terminated by addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The sGP130 concentration in each sample is interpolated from this standard curve.
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aaa17108 rat typical testing data standard curve for reference only aaa17108_td elisa kit soluble glucoprotein 130 sgp130 samples serum plasma cell culture supernatants body fluid and tissue homogenate assay type sandwich sensitivity 0.1 ng ml intended uses this is a 1.5 hour solid phase designed the quantitative determination of research use not therapeutic applications! glucoprotein130 sensitivity0.1 a1.5
⇄⧉search_terms => string (231) "aaa19082 human elisa kit soluble ox40l sox40l assay type quantitative sandwi...
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aaa19082 human elisa kit soluble ox40l sox40l assay type quantitative sandwich samples serum plasma cell culture supernates lysates tissue homogenates and other biological fluids detection range 0.05 ng ml 20 sensitivity 0.029 ml20
⇄⧉specificity => string (382) "This assay has high sensitivity and excellent specificity for detection of s...
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This assay has high sensitivity and excellent specificity for detection of sOX40L. No significant cross-reactivity or interference between sOX40L and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between sOX40L and all the analogues, therefore, cross reaction may still exist in some cases.
⇄purity => string (3) "N/A"
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⇄form => string (3) "N/A"
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⇄storage_stability => string (35) "Store all reagents at 2-8 degree C."
⇄⧉products_description => string (1416) "Principle of the Assay: sOX40L ELISA kit applies the competitive enzyme immu...
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Principle of the Assay: sOX40L ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-sOX40L antibody and an sOX40L-HRP conjugate. The assay sample and buffer are incubated together with sOX40L-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the sOX40L concentration since sOX40L from samples and sOX40L-HRP conjugate compete for the anti-sOX40L antibody binding site. Since the number of sites is limited, as more sites are occupied by sOX40L from the sample, fewer sites are left to bind sOX40L-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The sOX40L concentration in each sample is interpolated from this standard curve.<br><br>Intended Uses: This sOX40L ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Monkey sOX40L. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
⇄⧉search_terms => string (536) "aaa27156 monkey this assay has high sensitivity and excellent specificity fo...
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aaa27156 monkey this assay has high sensitivity and excellent specificity for detection of sox40l no significant cross reactivity or interference between analogues was observed note limited by current skills knowledge it is impossible us to complete the all therefore reaction may still exist in some cases typical testing data standard curve reference only aaa27156_sc elisa kit soluble ox40 ligand sox4l samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative competitive 0.1 ng ml competitive0.1
⇄⧉specificity => string (379) "This assay has high sensitivity and excellent specificity for detection of s...
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This assay has high sensitivity and excellent specificity for detection of sLEPR. No significant cross-reactivity or interference between sLEPR and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between sLEPR and all the analogues, therefore, cross reaction may still exist in some cases.
⇄purity => string (3) "N/A"
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⇄form => string (3) "N/A"
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⇄concentration => string (3) "N/A"
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⇄storage_stability => string (35) "Store all reagents at 2-8 degree C."
⇄⧉products_description => string (1396) "Intended Uses: This sLEPR ELISA kit is a 1.5 hour solid-phase ELISA designed...
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Intended Uses: This sLEPR ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Mouse sLEPR. This ELISA kit for research use only, not for therapeutic or test applications!<br><br>Principle of the Assay: sLEPR ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-sLEPR antibody and an sLEPR-HRP conjugate. The assay sample and buffer are incubated together with sLEPR-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the sLEPR concentration since sLEPR from samples and sLEPR-HRP conjugate compete for the anti-sLEPR antibody binding site. Since the number of sites is limited, as more sites are occupied by sLEPR from the sample, fewer sites are left to bind sLEPR-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The sLEPR concentration in each sample is interpolated from this standard curve.
⇄⧉search_terms => string (556) "aaa16027 mouse this assay has high sensitivity and excellent specificity for...
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aaa16027 mouse this assay has high sensitivity and excellent specificity for detection of slepr no significant cross reactivity or interference between analogues was observed note limited by current skills knowledge it is impossible us to complete the all therefore reaction may still exist in some cases typical testing data standard curve reference only aaa16027_sc elisa kit soluble leptin receptor slr signal transduction samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative competitive 0.1 ng ml competitive0.1
⇄⧉specificity => string (379) "This assay has high sensitivity and excellent specificity for detection of S...
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This assay has high sensitivity and excellent specificity for detection of SLEPR. No significant cross-reactivity or interference between SLEPR and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between SLEPR and all the analogues, therefore, cross reaction may still exist in some cases.
⇄purity => string (3) "N/A"
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⇄form => string (3) "N/A"
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⇄concentration => string (3) "N/A"
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⇄storage_stability => string (35) "Store all reagents at 2-8 degree C."
⇄⧉products_description => string (1400) "Principle of the Assay: SLEPR ELISA kit applies the competitive enzyme immun...
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Principle of the Assay: SLEPR ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-SLEPR antibody and an SLEPR-HRP conjugate. The assay sample and buffer are incubated together with SLEPR-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the SLEPR concentration since SLEPR from samples and SLEPR-HRP conjugate compete for the anti-SLEPR antibody binding site. Since the number of sites is limited, as more sites are occupied by SLEPR from the sample, fewer sites are left to bind SLEPR-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The SLEPR concentration in each sample is interpolated from this standard curve.<br><br>Intended Uses: This SLEPR ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Rat SLEPR. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
⇄⧉search_terms => string (554) "aaa16328 rat this assay has high sensitivity and excellent specificity for d...
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aaa16328 rat this assay has high sensitivity and excellent specificity for detection of slepr no significant cross reactivity or interference between analogues was observed note limited by current skills knowledge it is impossible us to complete the all therefore reaction may still exist in some cases typical testing data standard curve reference only aaa16328_sc elisa kit soluble leptin receptor slr signal transduction samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative competitive 0.1 ng ml competitive0.1
⇄⧉etc_term1 => string (133) "Samples||Serum, plasma, Cell Culture Supernatants, body fluid and tissue hom...
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Samples||Serum, plasma, Cell Culture Supernatants, body fluid and tissue homogenate!!Assay Type||Competitive!!Sensitivity||1.0 ng/mL.
⇄⧉etc_term2 => string (203) "Intended Uses||This sGP-130 ELISA kit is a 1.5 hour solid-phase ELISA design...
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Intended Uses||This sGP-130 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Mouse sGP-130. This ELISA kit for research use only, not for therapeutic applications!
⇄⧉products_description => string (1210) "<b>Principle of the assay: </b>sGP-130 ELISA kit applies the competitive enz...
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<b>Principle of the assay: </b>sGP-130 ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-sGP-130 antibody and an sGP-130-HRP conjugate. The assay sample and buffer are incubated together with sGP-130-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the sGP-130 concentration since sGP-130 from samples and sGP-130-HRP conjugate compete for the anti-sGP-130 antibody binding site. Since the number of sites is limited, as more sites are occupied by sGP-130 from the sample, fewer sites are left to bind sGP-130-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The sGP-130 concentration in each sample is interpolated from this standard curve.
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aaa17111 mouse typical testing data standard curve for reference only aaa17111_td elisa kit soluble glucoprotein 130 sgp130 samples serum plasma cell culture supernatants body fluid and tissue homogenate assay type competitive sensitivity 1.0 ng ml intended uses this sgp is a 1.5 hour solid phase designed the quantitative determination of research use not therapeutic applications! glucoprotein130 sensitivity1.0 a1.5
⇄⧉specificity => string (379) "This assay has high sensitivity and excellent specificity for detection of s...
$value[17]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of sTFeR. No significant cross-reactivity or interference between sTFeR and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between sTFeR and all the analogues, therefore, cross reaction may still exist in some cases.
⇄purity => string (3) "N/A"
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⇄form => string (3) "N/A"
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⇄concentration => string (3) "N/A"
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⇄storage_stability => string (35) "Store all reagents at 2-8 degree C."
⇄⧉products_description => string (1514) "Principle of the Assay: sTFeR ELISA kit applies the quantitative sandwich en...
$value[17]['_source']['products_description']
Principle of the Assay: sTFeR ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for sTFeR. Standards or samples are then added to the microtiter plate wells and sTFeR if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of sTFeR present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for sTFeR are added to each well to "sandwich" the sTFeR immobilized on the plate. The microtiter plate undergoes incubation, and then the wells are thoroughly washed to remove all unbound components. Next, substrate solutions are added to each well. The enzyme (HRP) and substrate are allowed to react over a short incubation period. Only those wells that contain sTFeR and enzyme-conjugated antibody will exhibit a change in color. The enzyme-substrate reaction is terminated by addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The sTFeR concentration in each sample is interpolated from this standard curve.<br><br>Intended Uses: This sTFeR ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Monkey sTFeR. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
⇄⧉search_terms => string (557) "aaa17165 monkey this assay has high sensitivity and excellent specificity fo...
$value[17]['_source']['search_terms']
aaa17165 monkey this assay has high sensitivity and excellent specificity for detection of stfer no significant cross reactivity or interference between analogues was observed note limited by current skills knowledge it is impossible us to complete the all therefore reaction may still exist in some cases typical testing data standard curve reference only aaa17165_sc elisa kit soluble transferrin receptor stfr signal transduction samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative sandwich 1.0 ng ml sandwich1.0
⇄⧉specificity => string (376) "This assay has high sensitivity and excellent specificity for detection of s...
$value[18]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of sTFR. No significant cross-reactivity or interference between sTFR and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between sTFR and all the analogues, therefore, cross reaction may still exist in some cases.
⇄purity => string (3) "N/A"
$value[18]['_source']['purity']
⇄form => string (3) "N/A"
$value[18]['_source']['form']
⇄concentration => string (3) "N/A"
$value[18]['_source']['concentration']
⇄storage_stability => string (35) "Store all reagents at 2-8 degree C."
⇄⧉products_description => string (1389) "Principle of the Assay: sTFR ELISA kit applies the competitive enzyme immuno...
$value[18]['_source']['products_description']
Principle of the Assay: sTFR ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-sTFR antibody and an sTFR-HRP conjugate. The assay sample and buffer are incubated together with sTFR-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the sTFR concentration since sTFR from samples and sTFR-HRP conjugate compete for the anti-sTFR antibody binding site. Since the number of sites is limited, as more sites are occupied by sTFR from the sample, fewer sites are left to bind sTFR-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The sTFR concentration in each sample is interpolated from this standard curve.<br><br>Intended Uses: This sTFR ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human sTFR. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
⇄⧉search_terms => string (556) "aaa17183 human this assay has high sensitivity and excellent specificity for...
$value[18]['_source']['search_terms']
aaa17183 human this assay has high sensitivity and excellent specificity for detection of stfr no significant cross reactivity or interference between analogues was observed note limited by current skills knowledge it is impossible us to complete the all therefore reaction may still exist in some cases typical testing data standard curve reference only aaa17183_sc elisa kit soluble transferrin receptor signal transduction samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative competitive 1.0 ng ml competitive1.0
⇄⧉specificity => string (385) "This assay has high sensitivity and excellent specificity for detection of S...
$value[19]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of SNKG2DL. No significant cross-reactivity or interference between SNKG2DL and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between SNKG2DL and all the analogues, therefore, cross reaction may still exist in some cases.
⇄purity => string (3) "N/A"
$value[19]['_source']['purity']
⇄form => string (3) "N/A"
$value[19]['_source']['form']
⇄concentration => string (3) "N/A"
$value[19]['_source']['concentration']
⇄storage_stability => string (35) "Store all reagents at 2-8 degree C."
⇄⧉products_description => string (1428) "Principle of the Assay: SNKG2DL ELISA kit applies the competitive enzyme imm...
$value[19]['_source']['products_description']
Principle of the Assay: SNKG2DL ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-SNKG2DL antibody and an SNKG2DL-HRP conjugate. The assay sample and buffer are incubated together with SNKG2DL-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the SNKG2DL concentration since SNKG2DL from samples and SNKG2DL-HRP conjugate compete for the anti-SNKG2DL antibody binding site. Since the number of sites is limited, as more sites are occupied by SNKG2DL from the sample, fewer sites are left to bind SNKG2DL-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The SNKG2DL concentration in each sample is interpolated from this standard curve.<br><br>Intended Uses: This SNKG2DL ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human SNKG2DL. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
⇄⧉search_terms => string (559) "aaa17071 human this assay has high sensitivity and excellent specificity for...
$value[19]['_source']['search_terms']
aaa17071 human this assay has high sensitivity and excellent specificity for detection of snkg2dl no significant cross reactivity or interference between analogues was observed note limited by current skills knowledge it is impossible us to complete the all therefore reaction may still exist in some cases typical testing data standard curve reference only aaa17071_sc elisa kit soluble nkg2d ligands nkg2dl signal transduction samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative competitive 0.1 ng ml competitive0.1
