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.
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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` = '21559'
AND `pd`.`language_id` = 1
LIMIT 1
Query
Database
1.94 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 = '21559' and pd.language_id = 1
Query
Database
1.38 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` = '21559'
Database (4 total Queries, 4 of them unique across 2 Connections)
Time
Query String
2.12 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` = '21559'
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 = '21559' 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` = '21559'
⇄⧉specificity => string (156) "This kit recognizes natural and recombinant Human PIGR/SC. No significant cr...
$value['specificity']
This kit recognizes natural and recombinant Human PIGR/SC. No significant cross-reactivity or interference between Human PIGR/SC and analogues was observed.
⇄purity => string (3) "N/A"
$value['purity']
⇄form => string (3) "N/A"
$value['form']
⇄concentration => string (3) "N/A"
$value['concentration']
⇄storage_stability => string (20) "Store at 4 degree C."
Human PIGR/SC (Polymeric Immunoglobulin Receptor/Membrane Secretory Component) ELISA Kit
⇄products_name_syn => string (3) "N/A"
$value['products_name_syn']
⇄products_gene_name => string (7) "PIGR/SC"
$value['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value['products_gene_name_syn']
⇄⧉products_description => string (1224) "Intended Uses||This ELISA kit applies to the in vitro quantitative determina...
$value['products_description']
Intended Uses||This ELISA kit applies to the in vitro quantitative determination of Human PIGR/SC concentrations in serum, plasma and other biological fluids.<br><br>Principle of the Assay: This ELISA kit uses Sandwich-ELISA as the method. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to PIGR/SC. Standards or samples are added to the appropriate micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for PIGR/SC and Avidin-Horseradish Peroxidase (HRP) conjugate is added to each micro plate well successively and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain PIGR/SC, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm +/- 2 nm. The OD value is proportional to the concentration of PIGR/SC. You can calculate the concentration of PIGR/SC in the samples by comparing the OD of the samples to the standard curve.
⇄products_references => string (3) "N/A"
$value['products_references']
⇄products_related_diseases => string (3) "N/A"
$value['products_related_diseases']
⇄products_categories => string (3) "N/A"
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⇄products_search_terms => 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"
$value['ncbi_protein_info']
⇄ncbi_chrom_loc => string (3) "N/A"
$value['ncbi_chrom_loc']
⇄ncbi_gene_id => string (3) "N/A"
$value['ncbi_gene_id']
⇄ncbi_mol_weight => string (3) "N/A"
$value['ncbi_mol_weight']
⇄ncbi_pathways => string (3) "N/A"
$value['ncbi_pathways']
⇄sp_protein_name => string (3) "N/A"
$value['sp_protein_name']
⇄sp_protein_name_syn => string (3) "N/A"
$value['sp_protein_name_syn']
⇄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"
$value['sp_interactions']
⇄products_url => string (3) "N/A"
$value['products_url']
⇄products_viewed => string (1) "0"
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⇄ncbi_summary_pdns => string (3) "N/A"
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⇄sp_comments_pdns => string (3) "N/A"
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$value['ncbi_research_articles_pdns']
⇄products_description_extra => string (3) "N/A"
$value['products_description_extra']
title
Human PIGR/SC ELISA Kit | PIGR/SC elisa kit
datasheet
⧉⌕$value App\Libraries\DatasheetLibrary (10)
Properties (10)
Available methods (45)
⇄⧉public a -> array (75)
$value->a
⇄products_id_mbs => string (7) "2504841"
$value->a['products_id_mbs']
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$value->a['products_id']
⇄products_quantity => string (4) "9999"
$value->a['products_quantity']
⇄products_model => string (8) "AAA21559"
$value->a['products_model']
⇄products_model_oem => string (10) "E-EL-H1236"
$value->a['products_model_oem']
⇄products_similar => string (3) "N/A"
$value->a['products_similar']
⇄ncbi_gi_num => string (3) "N/A"
$value->a['ncbi_gi_num']
⇄ncbi_acc_num => string (3) "N/A"
$value->a['ncbi_acc_num']
⇄ncbi_acc_num_related => string (3) "N/A"
$value->a['ncbi_acc_num_related']
⇄ncbi_sp_acc_num_related => string (3) "N/A"
$value->a['ncbi_sp_acc_num_related']
⇄ncbi_gb_acc_num => string (3) "N/A"
$value->a['ncbi_gb_acc_num']
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$value->a['sp_acc_num_syn']
⇄products_image => string (9) "ELISA Kit"
$value->a['products_image']
⇄sequence_positions => string (3) "N/A"
$value->a['sequence_positions']
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⇄clonality => string (3) "N/A"
$value->a['clonality']
⇄isotype => string (3) "N/A"
$value->a['isotype']
⇄clone_number => string (3) "N/A"
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⇄host => string (3) "N/A"
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⇄reactivity => string (5) "Human"
$value->a['reactivity']
⇄⧉specificity => string (156) "This kit recognizes natural and recombinant Human PIGR/SC. No significant cr...
$value->a['specificity']
This kit recognizes natural and recombinant Human PIGR/SC. No significant cross-reactivity or interference between Human PIGR/SC and analogues was observed.
⇄purity => string (3) "N/A"
$value->a['purity']
⇄form => string (3) "N/A"
$value->a['form']
⇄concentration => string (3) "N/A"
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⇄storage_stability => string (20) "Store at 4 degree C."
Human PIGR/SC (Polymeric Immunoglobulin Receptor/Membrane Secretory Component) ELISA Kit
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$value->a['products_name_syn']
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⇄products_gene_name_syn => string (3) "N/A"
$value->a['products_gene_name_syn']
⇄⧉products_description => string (1224) "Intended Uses||This ELISA kit applies to the in vitro quantitative determina...
$value->a['products_description']
Intended Uses||This ELISA kit applies to the in vitro quantitative determination of Human PIGR/SC concentrations in serum, plasma and other biological fluids.<br><br>Principle of the Assay: This ELISA kit uses Sandwich-ELISA as the method. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to PIGR/SC. Standards or samples are added to the appropriate micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for PIGR/SC and Avidin-Horseradish Peroxidase (HRP) conjugate is added to each micro plate well successively and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain PIGR/SC, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm +/- 2 nm. The OD value is proportional to the concentration of PIGR/SC. You can calculate the concentration of PIGR/SC in the samples by comparing the OD of the samples to the standard curve.
⇄products_references => string (3) "N/A"
$value->a['products_references']
⇄products_related_diseases => string (3) "N/A"
$value->a['products_related_diseases']
⇄products_categories => string (3) "N/A"
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⇄products_search_terms => string (3) "N/A"
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⇄ncbi_full_name => string (3) "N/A"
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$value->a['ncbi_symbol']
⇄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"
$value->a['ncbi_gene_id']
⇄ncbi_mol_weight => string (3) "N/A"
$value->a['ncbi_mol_weight']
⇄ncbi_pathways => string (3) "N/A"
$value->a['ncbi_pathways']
⇄sp_protein_name => string (3) "N/A"
$value->a['sp_protein_name']
⇄sp_protein_name_syn => string (3) "N/A"
$value->a['sp_protein_name_syn']
⇄sp_gene_name => string (3) "N/A"
$value->a['sp_gene_name']
⇄sp_gene_name_syn => string (3) "N/A"
$value->a['sp_gene_name_syn']
⇄sp_entry_name => string (3) "N/A"
$value->a['sp_entry_name']
⇄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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⇄ncbi_summary_pdns => string (3) "N/A"
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⇄sp_comments_pdns => string (3) "N/A"
$value->a['sp_comments_pdns']
⇄ncbi_research_articles_pdns => string (3) "N/A"
$value->a['ncbi_research_articles_pdns']
⇄products_description_extra => string (3) "N/A"
$value->a['products_description_extra']
⇄⧉public d -> array (75)
$value->d
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⇄products_id => string (5) "21559"
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⇄products_model => string (8) "AAA21559"
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⇄products_model_oem => string (10) "E-EL-H1236"
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⇄products_similar => string (3) "N/A"
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⇄ncbi_acc_num => string (3) "N/A"
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⇄ncbi_acc_num_related => string (3) "N/A"
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⇄ncbi_sp_acc_num_related => string (3) "N/A"
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⇄ncbi_gb_acc_num => string (3) "N/A"
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⇄sp_acc_num => string (3) "N/A"
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⇄sp_acc_num_syn => string (3) "N/A"
$value->d['sp_acc_num_syn']
⇄products_image => string (9) "ELISA Kit"
$value->d['products_image']
⇄sequence_positions => string (3) "N/A"
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⇄sequence_length => string (3) "N/A"
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⇄sequence => string (3) "N/A"
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⇄clonality => string (3) "N/A"
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⇄isotype => string (3) "N/A"
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⇄clone_number => string (3) "N/A"
$value->d['clone_number']
⇄host => string (3) "N/A"
$value->d['host']
⇄reactivity => string (5) "Human"
$value->d['reactivity']
⇄⧉specificity => string (156) "This kit recognizes natural and recombinant Human PIGR/SC. No significant cr...
$value->d['specificity']
This kit recognizes natural and recombinant Human PIGR/SC. No significant cross-reactivity or interference between Human PIGR/SC and analogues was observed.
⇄purity => string (3) "N/A"
$value->d['purity']
⇄form => string (3) "N/A"
$value->d['form']
⇄concentration => string (3) "N/A"
$value->d['concentration']
⇄storage_stability => string (20) "Store at 4 degree C."
Human PIGR/SC (Polymeric Immunoglobulin Receptor/Membrane Secretory Component) ELISA Kit
⇄products_name_syn => string (3) "N/A"
$value->d['products_name_syn']
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$value->d['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value->d['products_gene_name_syn']
⇄⧉products_description => string (1224) "Intended Uses||This ELISA kit applies to the in vitro quantitative determina...
$value->d['products_description']
Intended Uses||This ELISA kit applies to the in vitro quantitative determination of Human PIGR/SC concentrations in serum, plasma and other biological fluids.<br><br>Principle of the Assay: This ELISA kit uses Sandwich-ELISA as the method. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to PIGR/SC. Standards or samples are added to the appropriate micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for PIGR/SC and Avidin-Horseradish Peroxidase (HRP) conjugate is added to each micro plate well successively and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain PIGR/SC, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm +/- 2 nm. The OD value is proportional to the concentration of PIGR/SC. You can calculate the concentration of PIGR/SC in the samples by comparing the OD of the samples to the standard curve.
⇄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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⇄products_search_terms => string (3) "N/A"
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⇄ncbi_full_name => string (3) "N/A"
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⇄ncbi_symbol => string (3) "N/A"
$value->d['ncbi_symbol']
⇄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"
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⇄sp_gene_name => 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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⇄ncbi_summary_pdns => string (3) "N/A"
$value->d['ncbi_summary_pdns']
⇄sp_comments_pdns => string (3) "N/A"
$value->d['sp_comments_pdns']
⇄ncbi_research_articles_pdns => string (3) "N/A"
$value->d['ncbi_research_articles_pdns']
⇄products_description_extra => string (3) "N/A"
$value->d['products_description_extra']
⇄⧉public fields_below -> array (3)
$value->fields_below
⇄0 => string (31) "Related Product Information for"
⇄⧉products_description => string (824) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[0]['_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-Rat PGE2 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.
⇄⧉search_terms => string (402) "aaa12553 rat typical testing data standard curve for reference only aaa12553...
$value[0]['_source']['search_terms']
aaa12553 rat typical testing data standard curve for reference only aaa12553_sc elisa kit prostaglandin e2 pge2 receptor ep4 subtype e 4 ptger4 ep4r prostanoid pge 53,119 da ptger2 pe2r4_human 4506259 np_000949.1 p35408 nm_000958.2 q3mj87 601586 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 1000 pg ml 15.6 sensitivity up to 5 intra precision e4 to5
⇄⧉products_description => string (828) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[1]['_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 PGE2 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.
⇄⧉search_terms => string (443) "aaa12839 porcine no cross reaction with other factors typical testing data s...
$value[1]['_source']['search_terms']
aaa12839 porcine no cross reaction with other factors typical testing data standard curve for reference only aaa12839_sc elisa kit prostaglandin e2 pge2 receptor ep4 subtype e 4 ptger4 ep4r prostanoid pge 53,119 da ptger2 pe2r4_human 4506259 np_000949.1 p35408 nm_000958.2 q3mj87 601586 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 1000 pg ml 15.6 sensitivity up to 5 intra precision e4 to5
⇄⧉specificity => string (169) "This assay has high sensitivity and excellent specificity for detection of P...
$value[2]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of PGE2. No significant cross-reactivity or interference between PGE2 and analogues was observed.
⇄purity => string (3) "N/A"
$value[2]['_source']['purity']
⇄form => string (3) "N/A"
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Principle of the Assay: This kit was based on Competitive-ELISA detection method. The microtiter plate provided in this kit has been pre-coated with target. During the reaction, target in the sample or standard competes with a fixed amount of target on the solid phase supporter for sites on the Biotinylated Detection Antibody specific to target. Excess conjugate and unbound sample or standard are washed from the plate, and HRP-Streptavidin (SABC) is added to each microplate well and incubated. Then TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. The concentration of target in the samples is then determined by comparing the OD of the samples to the standard curve.
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aaa17546 general this assay has high sensitivity and excellent specificity for detection of pge2 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa17546_sc elisa kit prostaglandin e2 receptor ep4 subtype e 4 ptger4 ep4r 53,119 da prostanoid ptger2 pge pe2r4_human 4506259 np_000949.1 p35408 nm_000958.2 q3mj87 601586 samples serum plasma tissue homogenates other biological fluids type quantitative competitive range 31.25 2000pg ml 18.75pg intra precision cv e4
⇄⧉products_description => string (826) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
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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 PGE2 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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aaa12396 human typical testing data standard curve for reference only aaa12396_sc elisa kit prostaglandin e2 pge2 receptor ep4 subtype e 4 ptger4 ep4r prostanoid pge 53,119 da ptger2 pe2r4_human 4506259 np_000949.1 p35408 nm_000958.2 q3mj87 601586 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 500 pg ml 7.8 sensitivity up to 1 intra precision e4 range500 ml7.8 to1
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Intra-assay Precision||Intra-assay Precision (Precision within an assay): 3 samples with low, mid range and high level PGE2 were tested 20 times on one plate, respectively.!!Inter-assay Precision||Inter-assay Precision (Precision between assays): 3 samples with low, mid range and high level PGE2 were tested on 3 different plates, 20 replicates in each plate.
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Intended Uses: This ELISA kit applies to the in vitro quantitative determination of PGE2 concentrations in serum, plasma and other biological fluids.<br><br>Principle of the Assay: This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with PGE2. During the reaction, PGE2 in the sample or standard competes with a fixed amount of PGE2 on the solid phase supporter for sites on the Biotinylated Detection Ab specific to PGE2. Excess conjugate and unbound sample or standard are washed from the plate, and Avidin conjugated to Horseradish Peroxidase (HRP) are added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color change is measured spectrophotometrically at a wavelength of 450 nm +/- 2 nm. The concentration of PGE2 in the samples is then determined by comparing the OD of the samples to the standard curve.
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aaa21615 general this kit recognizes pge2 in samples no significant cross reactivity or interference between and analogues was observed typical testing data standard curve for reference only aaa21615_td elisa prostaglandin e2 receptor ep4 subtype e 4 ptger4 ep4r pge prostanoid 53,119 da ptger2 pe2r4_human 4506259 np_000949.1 p35408 nm_000958.2 q3mj87 601586 serum plasma other biological fluids assay type quantitative competitive detection range 31.25 2000pg ml sensitivity 18.75pg intra precision within an 3 with low mid high level were tested 20 times on one plate respectively inter assays different plates replicates each e4 an3 tested20
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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 PGE2 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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aaa12883 mouse typical testing data standard curve for reference only aaa12883_sc elisa kit prostaglandin e2 pge2 receptor ep4 subtype e 4 ptger4 ep4r prostanoid pge 53,119 da ptger2 pe2r4_human 4506259 np_000949.1 p35408 nm_000958.2 q3mj87 601586 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 500 pg ml 7.8 sensitivity up to 1 intra precision e4 range500 ml7.8 to1
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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-Chicken PGE2 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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aaa12786 chicken no cross reaction with other factors typical testing data standard curve for reference only aaa12786_sc elisa kit prostaglandin e2 pge2 receptor ep4 subtype e 4 ptger4 ep4r prostanoid pge 53,119 da ptger2 pe2r4_human 4506259 np_000949.1 p35408 nm_000958.2 q3mj87 601586 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 1000 pg ml 15.6pg sensitivity up to 5 intra precision e4 to5
⇄⧉products_description => string (858) "Intended Uses: This PGE2 competitive ELISA kit is intended for Laboratory Re...
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Intended Uses: This PGE2 competitive ELISA kit is intended for Laboratory Research use only and is not for use in diagnostic or therapeutic procedures. Add sample and PGE2 standards in the plate wells where PGE2 antibodies have been coated. Then add HRP-labeled mouse PGE2 antigen. The unreacted component will be removed after incubating and washing, and the solid-phase antibody-enzyme-labeled antigen immune complex on the solid surface of the microplate will remain. After adding Chromogen Solution A and Chromogen Solution B, the immune complex will change to blue by HRP catalyzing. It will change to yellow at the end when the adding stop solution works. Measure the absorbance (OD value) at 450 nm using a microtiter plate reader. The concentration of PGE2 in the samples is then determined by comparing the O.D. of the samples to the standard curve.
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aaa23722 mouse typical testing data standard curve for reference only aaa23722_sc elisa kit prostaglandin e2 pge2
⇄⧉products_description => string (1340) "Intended Uses: This PGE1 ELISA kit is a 1.5 hour solid-phase ELISA designed ...
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Intended Uses: This PGE1 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of MousePGE1. This ELISA kit for research use only!<br><br>Principle of the Assay: PGE1 ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-PGE1 antibody and an PGE1-HRP conjugate. The assay sample and buffer are incubated together with PGE1-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 PGE1 concentration since PGE1 from samples and PGE1-HRP conjugate compete for the anti-PGE1 antibody binding site. Since the number of sites is limited, as more sites are occupied by PGE1 from the sample, fewer sites are left to bind PGE1-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The PGE1 concentration in each sample is interpolated from this standard curve.
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aaa16811 bovine typical testing data standard curve for reference only aaa16811_sc elisa kit prostaglandin e2 pge2 samples serum plasma cell culture supernatants body fluid and tissue homogenate assay type quantitative competitive sensitivity 0.1 ng ml sensitivity0.1
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Assay Type||Competitive!!Samples||Serum, plasma, cell culture supernatant and other biological samples!!Detection Range||31.25-2000pg/ml!!Sensitivity||18.75pg/ml
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Intra-assay Precision||Intra-assay Precision: samples with low, medium and high concentration are tested 20 times on same plate.!!Inter-assay Precision||Inter-assay Precision: samples with low, medium and high concentration are tested 20 times on three different plates.
⇄⧉products_description => string (1929) "Background: Prostaglandin E2 (PGE2) is an important bioactive molecule and a...
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Background: Prostaglandin E2 (PGE2) is an important bioactive molecule and a member of the prostaglandin family. It is generated from arachidonic acid (AA) by the action of cyclooxygenase (COX). PGE2 is widely present in the Mammals body and can regulate various physiological and pathological processes, such as inflammation, immune response, pain perception, temperature regulation, and modulation of cardiovascular and digestive system function. PGE2 exerts its effects by binding to its four different types of receptors (EP1, EP2, EP3, EP4). Different types of receptors have distinct signal transduction pathways and functions, including regulation of cell proliferation, apoptosis, migration, invasion, cytokine release, and ion channel modulation. PGE2 plays an important role in the occurrence and development of many diseases, including inflammatory diseases, cancer, and cardiovascular diseases. Therefore, PGE2 and its receptors are important targets for researching and developing disease treatments.<br><br>Principle of the Assay: This kit was based on Competitive-ELISA detection method. The microtiter plate provided in this kit has been precoated with PGE2. During the reaction, PGE2 in the sample or standard competes with a fixed amount of PGE2 on the solid phase supporter for sites on the Biotinylated Detection Antibody specific to PGE2. Excess conjugate and unbound sample or standard are washed from the plate, and HRP-Streptavidin (SABC) is added to each microplate well and incubated. Then TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm. The concentration of PGE2 in the samples is then determined by comparing the OD of the samples to the standard curve. The concentration of the target substance was inversely proportional to the OD450 value.
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aaa27546 human this assay has high sensitivity and excellent specificity for detection of pge2 no significant cross reactivity or interference between analogues is observed typical testing data standard curve reference only aaa27546_sc elisa kit prostaglandin e2 pg type competitive
⇄⧉products_description => string (625) "Intended Uses: This PGE2 ELISA kit is intended Laboratory for Research use o...
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Intended Uses: This PGE2 ELISA kit is intended Laboratory for Research use only. The Stop Solution changes the color from blue to yellow and the intensity of the color is measured at 450 nm using a spectrophotometer. In order to measure the concentration of PGE2 in the sample, this PGE2 ELISA Kit includes a set of calibration standards. The calibration standards are assayed at the same time as the samples and allow the operator to produce a standard curve of Optical Density versus PGE2 concentration. The concentration of PGE2 in the samples is then determined by comparing the O.D. of the samples to the standard curve.
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aaa23638 human typical testing data standard curve for reference only aaa23638_sc elisa kit prostaglandin e2 pge2 sensitivity 1 pg ml intra assay precision cv less than 15 inter is sensitivity1 than15
⇄⧉products_description => string (1341) "Intended Uses: This PGE2 ELISA kit is a 1.5 hour solid-phase ELISA designed ...
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Intended Uses: This PGE2 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Horse PGE2. This ELISA kit for research use only!<br><br>Principle of the Assay: PGE2 ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-PGE2 antibody and an PGE2-HRP conjugate. The assay sample and buffer are incubated together with PGE2-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 PGE2 concentration since PGE2 from samples and PGE2-HRP conjugate compete for the anti-PGE2 antibody binding site. Since the number of sites is limited, as more sites are occupied by PGE2 from the sample, fewer sites are left to bind PGE2-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The PGE2 concentration in each sample is interpolated from this standard curve.
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aaa16698 typical testing data standard curve for reference only aaa16698_td elisa kit prostaglandin e2 pge2 horse samples serum plasma cell culture supernatants body fluid and tissue homogenate assay type quantitative competitive sensitivity 0.1 ng ml sensitivity0.1
⇄⧉specificity => string (169) "This assay has high sensitivity and excellent specificity for detection of P...
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This assay has high sensitivity and excellent specificity for detection of PGE2. No significant cross-reactivity or interference between PGE2 and analogues was observed.
⇄purity => string (3) "N/A"
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Assay Type||Competitive!!Samples||Serum, plasma, tissue homogenates and other biological fluids!!Detection Range||31.25-2000pg/ml!!Sensitivity||18.75pg/ml
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Principle of the Assay: This kit was based on Competitive-ELISA detection method. The microtiter plate provided in this kit has been pre-coated with target. During the reaction, target in the sample or standard competes with a fixed amount of target on the solid phase supporter for sites on the Biotinylated Detection Antibody specific to target. Excess conjugate and unbound sample or standard are washed from the plate, and HRP-Streptavidin (SABC) is added to each microplate well and incubated. Then TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm. The concentration of target in the samples is then determined by comparing the OD of the samples to the standard curve.
⇄⧉search_terms => string (399) "aaa27547 rat this assay has high sensitivity and excellent specificity for d...
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aaa27547 rat this assay has high sensitivity and excellent specificity for detection of pge2 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa27547_sc elisa kit prostaglandin e2 samples serum plasma other biological fluids type quantitative competitive range 31.25 2000pg ml 18.75pg intra precision cv<8 inter cv<10
Assay Type||Quantitative Sandwich!!Samples||Serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids!!Detection Range||20-4500ng/L!!Sensitivity||9.17ng/L
⇄⧉etc_term2 => string (403) "Intra-assay Precision||Intra-Assay Precision (Precision within an assay) Thr...
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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%
⇄⧉products_description => string (887) "Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (EL...
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Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (ELISA). The plate has been pre-coated with Rabbit PGE2 antibody. PGE2 present in the sample is added and binds to antibodies coated on the wells. And then biotinylated Rabbit PGE2 Antibody is added and binds to PGE2 in the sample. Then Streptavidin-HRP is added and binds to the Biotinylated PGE2 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 Rabbit PGE2. The reaction is terminated by addition of acidic stop solution and absorbance is measured at 450 nm.<br><br>Intended Uses: This sandwich kit is for the accurate quantitative detection of Rabbit Prostaglandin E2 (also known as PGE2) in serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids.
⇄⧉search_terms => string (459) "aaa18974 rabbit typical testing data standard curve for reference only aaa18...
$value[13]['_source']['search_terms']
aaa18974 rabbit typical testing data standard curve for reference only aaa18974_sc elisa kit prostaglandin e2 pge2 samples serum plasma cell culture supernates ascites tissue homogenates or other biological fluids assay type quantitative sandwich detection range 20 4500ng l sensitivity 9.17ng 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 range20 x100
⇄⧉specificity => string (169) "This assay has high sensitivity and excellent specificity for detection of P...
$value[14]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of PGE2. No significant cross-reactivity or interference between PGE2 and analogues was observed.
⇄purity => string (3) "N/A"
$value[14]['_source']['purity']
⇄form => string (3) "N/A"
$value[14]['_source']['form']
⇄concentration => string (3) "N/A"
$value[14]['_source']['concentration']
⇄⧉storage_stability => string (156) "Store entire kit at 2-8C for short-term. For longer-term, please store the m...
$value[14]['_source']['storage_stability']
Store entire kit at 2-8C for short-term. For longer-term, please store the microplate & standard at -20C, while the remaining reagents can be stored at 2-8C
Assay Type||Competitive!!Samples||Serum, plasma, tissue homogenates and other biological fluids!!Detection Range||31.25-2000pg/ml!!Sensitivity||18.75pg/ml
⇄⧉products_description => string (840) "Principle of the Assay: This kit was based on Competitive-ELISA detection me...
$value[14]['_source']['products_description']
Principle of the Assay: This kit was based on Competitive-ELISA detection method. The microtiter plate provided in this kit has been pre-coated with target. During the reaction, target in the sample or standard competes with a fixed amount of target on the solid phase supporter for sites on the Biotinylated Detection Antibody specific to target. Excess conjugate and unbound sample or standard are washed from the plate, and HRP-Streptavidin (SABC) is added to each microplate well and incubated. Then TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm. The concentration of target in the samples is then determined by comparing the OD of the samples to the standard curve.
⇄⧉search_terms => string (422) "aaa27549 porcine this assay has high sensitivity and excellent specificity f...
$value[14]['_source']['search_terms']
aaa27549 porcine this assay has high sensitivity and excellent specificity for detection of pge2 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa27549_sc elisa kit prostaglandin e2 samples serum plasma tissue homogenates other biological fluids type quantitative competitive range 31.25 2000pg ml 18.75pg intra precision cv<8 inter cv<10
⇄specificity => string (75) "Specifically recognize PGE2, no obvious cross reaction with other analogues"
$value[15]['_source']['specificity']
⇄purity => string (3) "N/A"
$value[15]['_source']['purity']
⇄form => string (3) "N/A"
$value[15]['_source']['form']
⇄concentration => string (3) "N/A"
$value[15]['_source']['concentration']
⇄⧉storage_stability => string (156) "Store entire kit at 2-8C for short-term. For longer-term, please store the m...
$value[15]['_source']['storage_stability']
Store entire kit at 2-8C for short-term. For longer-term, please store the microplate & standard at -20C, while the remaining reagents can be stored at 2-8C
Assay Type||Competitive!!Samples||Serum, plasma, cell culture supernatant and other biological samples!!Detection Range||31.25-2000pg/ml!!Sensitivity||18.75pg/ml
⇄⧉etc_term2 => string (270) "Intra-assay Precision||Intra-assay Precision: samples with low, medium and h...
$value[15]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision: samples with low, medium and high concentration are tested 20 times on same plate.!!Inter-assay Precision||Inter-assay Precision: samples with low, medium and high concentration are tested 20 times on three different plates.
⇄⧉products_description => string (1931) "Background: Prostaglandin E2 (PGE2) is an important bioactive molecule and a...
$value[15]['_source']['products_description']
Background: Prostaglandin E2 (PGE2) is an important bioactive molecule and a member of the prostaglandin family. It is generated from arachidonic acid (AA) by the action of cyclooxygenase (COX). PGE2 is widely present in the Mammals body and can regulate various physiological and pathological processes, such as inflammation, immune response, pain perception, temperature regulation, and modulation of cardiovascular and digestive system function. PGE2 exerts its effects by binding to its four different types of receptors (EP1, EP2, EP3, EP4). Different types of receptors have distinct signal transduction pathways and functions, including regulation of cell proliferation, apoptosis, migration, invasion, cytokine release, and ion channel modulation. PGE2 plays an important role in the occurrence and development of many diseases, including inflammatory diseases, cancer, and cardiovascular diseases. Therefore, PGE2 and its receptors are important targets for researching and developing disease treatments.<br><br>Principle of the Assay: This kit was based on Competitive-ELISA detection method. The microtiter plate provided in this kit has been pre-coated with PGE2. During the reaction, PGE2 in the sample or standard competes with a fixed amount of PGE2 on the solid phase supporter for sites on the Biotinylated Detection Antibody specific to PGE2. Excess conjugate and unbound sample or standard are washed from the plate, and HRP-Streptavidin (SABC) is added to each microplate well and incubated. Then TMB substrate solution is added to each well. The enzyme- substrate reaction is terminated by the addition of a acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm. The concentration of PGE2 in the samples is then determined by comparing the OD of the samples to the standard curve. The concentration of the target substance was inversely proportional to the OD450 value.
⇄⧉search_terms => string (420) "aaa17772 mouse this assay has high sensitivity and excellent specificity for...
$value[15]['_source']['search_terms']
aaa17772 mouse this assay has high sensitivity and excellent specificity for detection of pge2 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa17772_sc elisa kit prostaglandin e2 samples serum plasma tissue homogenates other biological fluids type quantitative competitive range 31.25 2000pg ml 18.75pg intra precision cv<8 inter cv<10
⇄⧉specificity => string (376) "This assay has high sensitivity and excellent specificity for detection of P...
$value[16]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of PGE2. No significant cross-reactivity or interference between PGE2 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between PGE2 and all the analogues, therefore, cross reaction may still exist in some cases.
⇄purity => string (3) "N/A"
$value[16]['_source']['purity']
⇄form => string (3) "N/A"
$value[16]['_source']['form']
⇄concentration => string (3) "N/A"
$value[16]['_source']['concentration']
⇄storage_stability => string (35) "Store all reagents at 2-8 degree C."
⇄⧉products_description => string (1387) "Principle of the Assay: PGE2 ELISA kit applies the competitive enzyme immuno...
$value[16]['_source']['products_description']
Principle of the Assay: PGE2 ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-PGE2 antibody and an PGE2-HRP conjugate. The assay sample and buffer are incubated together with PGE2-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 PGE2 concentration since PGE2 from samples and PGE2-HRP conjugate compete for the anti-PGE2 antibody binding site. Since the number of sites is limited, as more sites are occupied by PGE2 from the sample, fewer sites are left to bind PGE2-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The PGE2 concentration in each sample is interpolated from this standard curve.<br><br>Intended Uses: This PGE2 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Rat PGE2. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
⇄⧉search_terms => string (522) "aaa16527 rat this assay has high sensitivity and excellent specificity for d...
$value[16]['_source']['search_terms']
aaa16527 rat this assay has high sensitivity and excellent specificity for detection of pge2 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 aaa16527_sc elisa kit prostaglandin e2 samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative competitive 0.1 ng ml competitive0.1
⇄⧉specificity => string (376) "This assay has high sensitivity and excellent specificity for detection of P...
$value[17]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of PGE2. No significant cross-reactivity or interference between PGE2 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between PGE2 and all the analogues, therefore, cross reaction may still exist in some cases.
⇄purity => string (3) "N/A"
$value[17]['_source']['purity']
⇄form => string (3) "N/A"
$value[17]['_source']['form']
⇄concentration => string (3) "N/A"
$value[17]['_source']['concentration']
⇄storage_stability => string (35) "Store all reagents at 2-8 degree C."
⇄⧉products_description => string (1391) "Principle of the Assay: PGE2 ELISA kit applies the competitive enzyme immuno...
$value[17]['_source']['products_description']
Principle of the Assay: PGE2 ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-PGE2 antibody and an PGE2-HRP conjugate. The assay sample and buffer are incubated together with PGE2-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 PGE2 concentration since PGE2 from samples and PGE2-HRP conjugate compete for the anti-PGE2 antibody binding site. Since the number of sites is limited, as more sites are occupied by PGE2 from the sample, fewer sites are left to bind PGE2-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The PGE2 concentration in each sample is interpolated from this standard curve.<br><br>Intended Uses: This PGE2 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Porcine PGE2. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
⇄⧉search_terms => string (526) "aaa16857 porcine this assay has high sensitivity and excellent specificity f...
$value[17]['_source']['search_terms']
aaa16857 porcine this assay has high sensitivity and excellent specificity for detection of pge2 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 aaa16857_sc elisa kit prostaglandin e2 samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative competitive 0.1 ng ml competitive0.1
⇄⧉specificity => string (376) "This assay has high sensitivity and excellent specificity for detection of P...
$value[18]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of PGE2. No significant cross-reactivity or interference between PGE2 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between PGE2 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 (1390) "Principle of the Assay: PGE2 ELISA kit applies the competitive enzyme immuno...
$value[18]['_source']['products_description']
Principle of the Assay: PGE2 ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-PGE2 antibody and an PGE2-HRP conjugate. The assay sample and buffer are incubated together with PGE2-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 PGE2 concentration since PGE2 from samples and PGE2-HRP conjugate compete for the anti-PGE2 antibody binding site. Since the number of sites is limited, as more sites are occupied by PGE2 from the sample, fewer sites are left to bind PGE2-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The PGE2 concentration in each sample is interpolated from this standard curve.<br><br>Intended Uses: This PGE2 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Canine PGE2. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
⇄⧉search_terms => string (525) "aaa16741 canine this assay has high sensitivity and excellent specificity fo...
$value[18]['_source']['search_terms']
aaa16741 canine this assay has high sensitivity and excellent specificity for detection of pge2 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 aaa16741_sc elisa kit prostaglandin e2 samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative competitive 0.1 ng ml competitive0.1
⇄⧉specificity => string (376) "This assay has high sensitivity and excellent specificity for detection of P...
$value[19]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of PGE2. No significant cross-reactivity or interference between PGE2 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between PGE2 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 (1389) "Principle of the Assay: PGE2 ELISA kit applies the competitive enzyme immuno...
$value[19]['_source']['products_description']
Principle of the Assay: PGE2 ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-PGE2 antibody and an PGE2-HRP conjugate. The assay sample and buffer are incubated together with PGE2-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 PGE2 concentration since PGE2 from samples and PGE2-HRP conjugate compete for the anti-PGE2 antibody binding site. Since the number of sites is limited, as more sites are occupied by PGE2 from the sample, fewer sites are left to bind PGE2-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The PGE2 concentration in each sample is interpolated from this standard curve.<br><br>Intended Uses: This PGE2 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Mouse PGE2. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
⇄⧉search_terms => string (524) "aaa16469 mouse this assay has high sensitivity and excellent specificity for...
$value[19]['_source']['search_terms']
aaa16469 mouse this assay has high sensitivity and excellent specificity for detection of pge2 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 aaa16469_sc elisa kit prostaglandin e2 samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative competitive 0.1 ng ml competitive0.1
