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` = '17476'
AND `pd`.`language_id` = 1
LIMIT 1
Query
Database
10.64 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 = '17476' and pd.language_id = 1
Query
Database
2.63 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` = '17476'
Database (4 total Queries, 4 of them unique across 2 Connections)
Time
Query String
4.18 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` = '17476'
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 = '17476' 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` = '17476'
⇄⧉specificity => string (167) "This assay has high sensitivity and excellent specificity for detection of A...
$value['specificity']
This assay has high sensitivity and excellent specificity for detection of ADP. No significant cross-reactivity or interference between ADP 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 (156) "Store entire kit at 2-8C for short-term. For longer-term, please store the m...
$value['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
⇄⧉products_description => string (825) "Principle of the Assay: This kit was based on sandwich enzyme-linked immune-...
$value['products_description']
Principle of the Assay: This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Capture antibody was pre-coated onto 96-well plates. And the biotin conjugated antibody was used as detection antibodies. The standards, test samples and biotin conjugated detection antibody were added to the wells subsequently, and washed with wash buffer. HRP-Streptavidin was added and unbound conjugates were washed away with wash buffer. TMB substrates were used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the target amount of sample captured in plate. Read the O.D. absorbance at 450nm in a microplate reader, and then the concentration of target can be calculated.
⇄⧉specificity => string (167) "This assay has high sensitivity and excellent specificity for detection of A...
$value->a['specificity']
This assay has high sensitivity and excellent specificity for detection of ADP. No significant cross-reactivity or interference between ADP 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"
$value->a['concentration']
⇄⧉storage_stability => string (156) "Store entire kit at 2-8C for short-term. For longer-term, please store the m...
$value->a['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
⇄⧉products_description => string (825) "Principle of the Assay: This kit was based on sandwich enzyme-linked immune-...
$value->a['products_description']
Principle of the Assay: This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Capture antibody was pre-coated onto 96-well plates. And the biotin conjugated antibody was used as detection antibodies. The standards, test samples and biotin conjugated detection antibody were added to the wells subsequently, and washed with wash buffer. HRP-Streptavidin was added and unbound conjugates were washed away with wash buffer. TMB substrates were used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the target amount of sample captured in plate. Read the O.D. absorbance at 450nm in a microplate reader, and then the concentration of target can be calculated.
⇄⧉specificity => string (167) "This assay has high sensitivity and excellent specificity for detection of A...
$value->d['specificity']
This assay has high sensitivity and excellent specificity for detection of ADP. No significant cross-reactivity or interference between ADP 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 (156) "Store entire kit at 2-8C for short-term. For longer-term, please store the m...
$value->d['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
⇄⧉products_description => string (825) "Principle of the Assay: This kit was based on sandwich enzyme-linked immune-...
$value->d['products_description']
Principle of the Assay: This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Capture antibody was pre-coated onto 96-well plates. And the biotin conjugated antibody was used as detection antibodies. The standards, test samples and biotin conjugated detection antibody were added to the wells subsequently, and washed with wash buffer. HRP-Streptavidin was added and unbound conjugates were washed away with wash buffer. TMB substrates were used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the target amount of sample captured in plate. Read the O.D. absorbance at 450nm in a microplate reader, and then the concentration of target can be calculated.
⇄⧉specificity => string (183) "This assay has high sensitivity and excellent specificity for detection of m...
$value[0]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of mouse PROK2. No significant cross-reactivity or interference between mouse PROK2 and analogues was observed.
⇄purity => string (3) "N/A"
$value[0]['_source']['purity']
⇄form => string (3) "N/A"
$value[0]['_source']['form']
⇄concentration => string (3) "N/A"
$value[0]['_source']['concentration']
⇄⧉storage_stability => string (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[0]['_source']['storage_stability']
Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please refer to pdf manual for further storage instructions.
⇄⧉etc_term2 => string (327) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV...
$value[0]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV%<8%. Three samples of known concentration were tested twenty times on one plate to assess.!!Inter-assay Precision||Inter-assay Precision (Precision between assays): CV%<10%. Three samples of known concentration were tested in twenty assays to assess.
⇄⧉products_description => string (735) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value[0]['_source']['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for PROK2 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any PROK2 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for PROK2 is added to the wells. After washing, avidin 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 PROK2 bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄⧉search_terms => string (714) "aaa18317 mouse this assay has high sensitivity and excellent specificity for...
$value[0]['_source']['search_terms']
aaa18317 mouse this assay has high sensitivity and excellent specificity for detection of prok2 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa18317_td elisa kit prokineticin 2 bv8 kal4 mit1 pk2 protein homolog isoform prok1 1 bombina variegata 8 kd 8kda bv 14,185 da prok2_mouse 82830395 np_001032628.1 q9qxu7 nm_001037539.2 q9qxu5 q9qxu6 b7zmx7 samples serum plasma cell culture supernates tissue homogenates type quantitative sandwich range 12.5 pg ml 800 <3.12 intra precision within an cv <8 three known concentration were tested twenty times on one plate to assess inter assays <10 in prokineticin2 prok11 variegata8 ml800
⇄⧉specificity => string (167) "This assay has high sensitivity and excellent specificity for detection of P...
$value[1]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of PK2. No significant cross-reactivity or interference between PK2 and analogues was observed.
⇄purity => string (3) "N/A"
$value[1]['_source']['purity']
⇄form => string (3) "N/A"
$value[1]['_source']['form']
⇄concentration => string (3) "N/A"
$value[1]['_source']['concentration']
⇄⧉storage_stability => string (475) "The stability of kit is determined by the loss rate of activity. The loss ra...
$value[1]['_source']['storage_stability']
The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. <br>To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.
Assay Type||Quantitative Competitive!!Samples||Mouse serum, plasma and other biological fluids!!Detection Range||49.4-4,000pg/mL!!Sensitivity||< 19.1pg/mL
⇄⧉etc_term2 => string (412) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): 3 ...
$value[1]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level PK2 were tested 20 times on one plate, respectively. Intra-Assay: CV<10%!!Inter-assay Precision||Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level PK2 were tested on 3 different plates, 8 replicates in each plate. CV(%) = SD/meanX100. Inter-Assay: CV<12%
⇄⧉products_description => string (915) "Principle of the Assay: This assay employs the competitive inhibition enzyme...
$value[1]['_source']['products_description']
Principle of the Assay: This assay employs the competitive inhibition enzyme immunoassay technique. An antibody specific to PK2 has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled PK2 and unlabeled PK2 (Standards or samples) with the pre-coated antibody specific to PK2. After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of PK2 in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of PK2 in the sample.<br><br>Intended Uses: The kit is a competitive inhibition enzyme immunoassay technique for the in vitro quantitative measurement of PK2 in mouse serum, plasma and other biological fluids.
⇄products_references => string (3) "N/A"
$value[1]['_source']['products_references']
⇄⧉products_related_diseases => string (235) "Kallmann Syndrome||53!!Nervous System Diseases||30!!Inflammation||16!!Idiopa...
⇄⧉search_terms => string (649) "aaa20752 mouse this assay has high sensitivity and excellent specificity for...
$value[1]['_source']['search_terms']
aaa20752 mouse this assay has high sensitivity and excellent specificity for detection of pk2 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa20752_sc elisa kit prokineticin 2 pk bv8 mit1 kal4 protein homolog isoform a prok2 hh4 11,659 da prok2_human 187167261 np_001119600.1 q9hc23 nm_001126128.1 q53z79 q6isr0 607002 neuroscience samples serum plasma other biological fluids type quantitative competitive range 49.4 4,000pg ml < 17.7pg intra precision within an 3 with low middle level were tested 20 times on one plate respectively cv prokineticin2 an3 tested20
⇄⧉specificity => string (167) "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 PK2. No significant cross-reactivity or interference between PK2 and analogues was observed.
⇄purity => string (3) "N/A"
$value[2]['_source']['purity']
⇄form => string (3) "N/A"
$value[2]['_source']['form']
⇄concentration => string (3) "N/A"
$value[2]['_source']['concentration']
⇄⧉storage_stability => string (475) "The stability of kit is determined by the loss rate of activity. The loss ra...
$value[2]['_source']['storage_stability']
The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. <br>To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.
Assay Type||Quantitative Competitive!!Samples||Human serum, plasma and other biological fluids!!Detection Range||246.9-20,000pg/mL!!Sensitivity||< 89.5pg/mL
⇄⧉etc_term2 => string (412) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): 3 ...
$value[2]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level PK2 were tested 20 times on one plate, respectively. Intra-Assay: CV<10%!!Inter-assay Precision||Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level PK2 were tested on 3 different plates, 8 replicates in each plate. CV(%) = SD/meanX100. Inter-Assay: CV<12%
⇄⧉products_description => string (925) "Principle of the Assay: This assay employs the competitive inhibition enzyme...
$value[2]['_source']['products_description']
Principle of the Assay: This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to PK2 has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled PK2 and unlabeled PK2 (Standards or samples) with the pre-coated antibody specific to PK2. After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of PK2 in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of PK2 in the sample.<br><br>Intended Uses: The kit is a competitive inhibition enzyme immunoassay technique for the in vitro quantitative measurement of PK2 in human serum, plasma and other biological fluids.
<a href="https://www.hindawi.com/journals/ije/2021/6630102/" target="_blank">Circulating Prokineticin 2 Levels Are Increased in Children with Obesity and Correlated with Insulin Resistance; Int J Endocrinol; 2021 Apr 4;2021:6630102.; PMID: 33883996</a>; Han Wang; Department of Clinical Laboratory, Children"s Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Pediatrics, Chongqing Key Laboratory of Child Health and Nutrition, Chongqing 400014, China.
⇄⧉products_related_diseases => string (235) "Kallmann Syndrome||53!!Nervous System Diseases||30!!Inflammation||16!!Idiopa...
⇄⧉search_terms => string (649) "aaa20604 human this assay has high sensitivity and excellent specificity for...
$value[2]['_source']['search_terms']
aaa20604 human this assay has high sensitivity and excellent specificity for detection of pk2 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa20604_sc elisa kit prokineticin 2 pk bv8 mit1 kal4 protein homolog isoform a prok2 hh4 11,659 da prok2_human 187167261 np_001119600.1 q9hc23 nm_001126128.1 q53z79 q6isr0 607002 neuroscience samples serum plasma other biological fluids type quantitative competitive range 49.4 4,000pg ml < 18.2pg intra precision within an 3 with low middle level were tested 20 times on one plate respectively cv prokineticin2 an3 tested20
⇄specificity => string (77) "Specifically recognize TAGLN2, no obvious cross reaction with other analogues"
$value[3]['_source']['specificity']
⇄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 (156) "Store entire kit at 2-8C for short-term. For longer-term, please store the m...
$value[3]['_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||Sandwich!!Samples||Serum, plasma, cell culture supernatant and other biological samples!!Detection Range||0.156-10ng/ml!!Sensitivity||0.094ng/ml
⇄⧉etc_term2 => string (270) "Intra-assay Precision||Intra-assay Precision: samples with low, medium and h...
$value[3]['_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 (1319) "Background: Transgelin 2 (TAGLN2) is an actin binding protein with roles in ...
$value[3]['_source']['products_description']
Background: Transgelin 2 (TAGLN2) is an actin binding protein with roles in migration and invasion of cancer cells. Transgelin 2 plays a role in Toll-like receptor (TLR)-stimulated phagocytosis by macrophages, and regulates T cell activation. High expression of transgelin-2 indicates poor prognosis in diabetes-associated pancreatic ductal adenocarcinoma.<br><br>Principle of the Assay: This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Anti TAGLN2 antibody was pre-coated onto the 96-well plate. The biotin conjugated anti TAGLN2 antibody was used as the detection antibody. The standards and pilot samples were added to the wells subsequently. After incubation, unbound conjugates were removed by wash buffer. Then, biotinylated detection antibody was added to bind with TAGLN2 conjugated on coated antibody. After washing off unbound conjugates, HRP-Streptavidin was added. After a third washing, TMB substrates were added to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that turned yellow after adding a stop solution. Read the O.D. absorbance at 450nm in a microplate reader. The concentration of TAGLN2 in the sample was calculated by drawing a standard curve. The concentration of the target substance is proportional to the OD450 value.
⇄products_references => string (3) "N/A"
$value[3]['_source']['products_references']
⇄⧉products_related_diseases => string (208) "Nervous System Diseases||5!!Neoplasm Metastasis||4!!Liver Diseases||3!!Liver...
$value[3]['_source']['products_related_diseases']
Nervous System Diseases||5!!Neoplasm Metastasis||4!!Liver Diseases||3!!Liver Neoplasms||3!!Neural Tube Defects||3!!Brain Diseases||2!!Fibrosis||2!!Carcinoma, Hepatocellular||2!!Hyperplasia||1!!Inflammation||1
⇄⧉search_terms => string (591) "aaa17634 human this assay has high sensitivity and excellent specificity for...
$value[3]['_source']['search_terms']
aaa17634 human this assay has high sensitivity and excellent specificity for detection of tagln2 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa17634_sc elisa kit transgelin 2 sm22 alpha homolog isoform b ha1756 24,454 da epididymis tissue protein li 7e kiaa0120 tagl2_human 4507357 np_003555.1 p37802 nm_003564.2 q5jrq6 q5jrq7 q6fgi1 q9buh5 q9h4p0 e9kl39 604634 samples serum plasma homogenates other biological fluids type quantitative sandwich range 0.156 10ng ml 0.094ng intra precision cv transgelin2
⇄⧉specificity => string (239) "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 Hamster (Mesocricetus; Cricetulus)PLBD2. No significant cross-reactivity or interference between Hamster (Mesocricetus; Cricetulus)PLBD2 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 (69) "Samples||Serum, Plasma, Other biological fluids!!Assay Type||Sandwich"
Sample Volume||1-200 uL!!Precision||Intra-assay Precision (Precision within an assay)<br>Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision.<br>Inter-assay Precision (Precision between assays)<br>Three samples of known concentration were tested in forty separate assays to assess inter-assay precision.<br>CV (%) = SD/meanX100<br>Intra-Assay: CV<br>Inter-Assay: CV!!Detection Wavelength||450 nm
Most soluble lysosomal proteins carry Man6P (mannose 6-phosphate), a specific carbohydrate marker that enables their binding to cellular MPRs (Man6P receptors) and their subsequent targeting towards the lysosome.<br>This characteristic was exploited to identify novel soluble lysosomal proteins by proteomic analysis of Man6P proteins purified from a human cell line. The presence of Man6P sugars was confirmed by an MPR overlay experiment, which showed the direct and Man6P-dependent interaction between p76 and the MPR. The presence of six N-glycosylation sites was validated by progressive peptide-N-glycosidase F deglycosylation. Experiments using N- and C-termini directed anti-p76 antibodies provided insights into p76 maturation.<br><br>Principle of the Assay: This assay employs a two-site sandwich ELISA to quantitate PLBD2 in samples. An antibody specific for PLBD2 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyPLBD2 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for PLBD2 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 PLBD2 bound in the initial step. The color development is stopped and the intensity of the color is measured.
76 kDa protein; p76; LAMA-like protein 2; Lamina ancestor homolog 2; Phospholipase B domain-containing protein 2Cleaved into the following 2 chains:Putative phospholipase B-like 2 32 kDa form; Putative phospholipase B-like 2 45 kDa form
⇄sp_gene_name => string (5) "PLBD2"
$value[4]['_source']['sp_gene_name']
⇄sp_gene_name_syn => string (3) "p76"
$value[4]['_source']['sp_gene_name_syn']
⇄sp_entry_name => string (11) "PLBL2_HUMAN"
$value[4]['_source']['sp_entry_name']
⇄sp_mim => string (3) "N/A"
$value[4]['_source']['sp_mim']
⇄sp_interactions => string (3) "N/A"
$value[4]['_source']['sp_interactions']
⇄products_url => string (3) "N/A"
$value[4]['_source']['products_url']
⇄products_viewed => string (1) "0"
$value[4]['_source']['products_viewed']
⇄⧉search_terms => string (800) "aaa13241 hamster this assay has high sensitivity and excellent specificity f...
$value[4]['_source']['search_terms']
aaa13241 hamster this assay has high sensitivity and excellent specificity for detection of mesocricetus cricetulus plbd2 no significant cross reactivity or interference between analogues was observed elisa kit putative phospholipase b like 2 isoform 1 domain containing p76 plb homolog 76 kda protein lama lamina ancestor 32 form 45 mannose 6 phosphate associated 61,885 da 2cleaved into the following chains:putative plbl2_human 229093316 np_775813.2 q8nhp8 nm_173542.3 f5h5e2 samples serum plasma other biological fluids type sandwich sample volume 200 ul precision intra within an three known concentration were tested twenty times on one plate to assess inter assays in forty separate cv = sd meanx100 wavelength 450 nm like2 isoform1 homolog76 ancestor32 form45 mannose6 volume200 wavelength450
⇄⧉specificity => string (183) "This assay has high sensitivity and excellent specificity for detection of h...
$value[5]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of human Slit2. No significant cross-reactivity or interference between human Slit2 and analogues was observed.
⇄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 (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[5]['_source']['storage_stability']
Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please refer to pdf manual for further storage instructions.
⇄⧉etc_term2 => string (327) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV...
$value[5]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV%<8%. Three samples of known concentration were tested twenty times on one plate to assess.!!Inter-assay Precision||Inter-assay Precision (Precision between assays): CV%<10%. Three samples of known concentration were tested in twenty assays to assess.
⇄⧉products_description => string (735) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value[5]['_source']['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for Slit2 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any Slit2 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for Slit2 is added to the wells. After washing, avidin 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 Slit2 bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄products_references => string (3) "N/A"
$value[5]['_source']['products_references']
⇄⧉products_related_diseases => string (227) "Breast Neoplasms||23!!Nervous System Diseases||20!!Lung Neoplasms||16!!Skin ...
$value[5]['_source']['products_related_diseases']
Breast Neoplasms||23!!Nervous System Diseases||20!!Lung Neoplasms||16!!Skin Diseases||15!!Neoplasm Metastasis||13!!Brain Diseases||11!!Inflammation||10!!Liver Diseases||6!!Disease Models, Animal||6!!Small Cell Lung Carcinoma||6
⇄products_categories => string (3) "N/A"
$value[5]['_source']['products_categories']
⇄ncbi_full_name => string (32) "slit homolog 2 protein isoform 2"
Activation Of Rac Pathway||119530!!Axon Guidance Pathway||83065!!Axon Guidance Pathway||476!!Axon Guidance Pathway||105688!!Developmental Biology Pathway||477129!!Glypican 1 Network Pathway||138010!!Inactivation Of Cdc42 And Rac Pathway||119529!!Netrin-1 Signaling Pathway||160999!!Regulation Of Commissural Axon Pathfinding By Slit And Robo Pathway||119528!!Role Of Abl In Robo-Slit Signaling Pathway||119531
⇄⧉search_terms => string (532) "aaa15513 human this assay has high sensitivity and excellent specificity for...
$value[5]['_source']['search_terms']
aaa15513 human this assay has high sensitivity and excellent specificity for detection of slit2 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa15513_td elisa kit slit homolog 2 drosophila flj14420 slil3 protein isoform 169,870 da slit2_human 574281850 np_001276064.1 o94813 nm_001289135.1 o95710 q17ru3 q9y5q7 b7zlr5 603746 samples serum plasma tissue homogenates type sandwich range 0.78 ng ml 50 0.195 intra precision within an cv homolog2 ml50
⇄⧉specificity => string (183) "This assay has high sensitivity and excellent specificity for detection of h...
$value[6]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of human M2-PK. No significant cross-reactivity or interference between human M2-PK and analogues was observed.
⇄purity => string (3) "N/A"
$value[6]['_source']['purity']
⇄form => string (3) "N/A"
$value[6]['_source']['form']
⇄concentration => string (3) "N/A"
$value[6]['_source']['concentration']
⇄⧉storage_stability => string (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[6]['_source']['storage_stability']
Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please refer to pdf manual for further storage instructions.
⇄⧉etc_term2 => string (327) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV...
$value[6]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV%<8%. Three samples of known concentration were tested twenty times on one plate to assess.!!Inter-assay Precision||Inter-assay Precision (Precision between assays): CV%<10%. Three samples of known concentration were tested in twenty assays to assess.
⇄⧉products_description => string (735) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value[6]['_source']['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for M2-PK has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any M2-PK present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for M2-PK is added to the wells. After washing, avidin 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 M2-PK bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄products_references => string (3) "N/A"
$value[6]['_source']['products_references']
⇄⧉products_related_diseases => string (204) "Nervous System Diseases||11!!Lung Diseases||8!!Brain Diseases||8!!Fibrosis||...
$value[6]['_source']['products_related_diseases']
Nervous System Diseases||11!!Lung Diseases||8!!Brain Diseases||8!!Fibrosis||8!!Inflammation||6!!Cardiovascular Diseases||6!!Cell Transformation, Neoplastic||5!!Necrosis||4!!Liver Diseases||4!!Carcinoma||3
⇄⧉search_terms => string (774) "aaa14969 human this assay has high sensitivity and excellent specificity for...
$value[6]['_source']['search_terms']
aaa14969 human this assay has high sensitivity and excellent specificity for detection of m2 pk no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa14969_td elisa kit pyruvate kinase muscle cthbp mgc3932 oip3 pk3 pkm tcb thbp1 opa interacting protein 3 type thyroid hormone binding cytosolic pkm2 isoform c hel s 30 p58 oip tumor 2 isozymes m1 isozyme 1 epididymis secretory li 57,937 da pk2 kpym_human 332164775 np_001193725.1 p14618 nm_001206796.1 p14786 q53gk4 q96e76 q9bwb5 q9ucv6 q9upf2 a6nfk3 b2r5n8 b3kry0 b4dfx8 b4duu6 179050 samples serum plasma tissue homogenates quantitative sandwich range 0.9 u ml 60 < 0.225 intra precision within an cv protein3 s30 tumor2 isozyme1 range0.9 ml60
⇄⧉specificity => string (167) "This assay has high sensitivity and excellent specificity for detection of P...
$value[7]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of PIP. No significant cross-reactivity or interference between PIP and analogues was observed.
⇄purity => string (3) "N/A"
$value[7]['_source']['purity']
⇄form => string (3) "N/A"
$value[7]['_source']['form']
⇄concentration => string (3) "N/A"
$value[7]['_source']['concentration']
⇄⧉storage_stability => string (202) "For unopened kit, all reagents should be kept according to the labels on via...
$value[7]['_source']['storage_stability']
For unopened kit, all reagents should be kept according to the labels on vials. The TMB Substrate, Wash Buffer, Stop Solution should be stored at 4 degree C. All others should be stored at -20 degree C.
⇄⧉etc_term1 => string (168) "Samples||Human Serum, Plasma, Tissue Homogenates Or Other Biological Fluids!...
$value[7]['_source']['etc_term1']
Samples||Human Serum, Plasma, Tissue Homogenates Or Other Biological Fluids!!Assay Type||Quantitative Sandwich!!Detection Range||0.156-10ng/mL!!Sensitivity||0.061ng/mL.
⇄⧉etc_term2 => string (412) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): 3 ...
$value[7]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level PIP were tested 20 times on one plate, respectively. Intra-Assay: CV<10%!!Inter-assay Precision||Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level PIP were tested on 3 different plates, 8 replicates in each plate. CV(%) = SD/meanX100. Inter-Assay: CV<12%
⇄⧉products_description => string (1006) "Intended Uses: The kit is a sandwich enzyme immunoassay for the in vitro qua...
$value[7]['_source']['products_description']
Intended Uses: The kit is a sandwich enzyme immunoassay for the in vitro quantitative measurement of PIP in human serum, plasma, tissue homogenates or other biological fluids.<br><br>Principle of the Assay: The microtiter plate provided in this kit has been pre-coated with an antibody specific to PIP. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific to PIP. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain PIP, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm +/- 10nm. The concentration of PIP in the samples is then determined by comparing the O.D. of the samples to the standard curve.
⇄products_references => string (3) "N/A"
$value[7]['_source']['products_references']
⇄⧉products_related_diseases => string (204) "Nervous System Diseases||17!!Carcinoma||14!!Inflammation||9!!Fibrosis||8!!Ce...
$value[7]['_source']['products_related_diseases']
Nervous System Diseases||17!!Carcinoma||14!!Inflammation||9!!Fibrosis||8!!Cell Transformation, Neoplastic||8!!Necrosis||6!!Liver Diseases||5!!Breast Neoplasms||4!!Disease Models, Animal||4!!Weight Loss||3
⇄⧉search_terms => string (830) "aaa13913 human this assay has high sensitivity and excellent specificity for...
$value[7]['_source']['search_terms']
aaa13913 human this assay has high sensitivity and excellent specificity for detection of pip no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa13913_sc elisa kit pyruvate kinase muscle pkm2 m2pk pkm m2 pk pkm1 cthbp oip3 pk3 tcb thbp1 isozyme thyroid hormone binding protein 1 cytosolic isoform c hel s 30 56,273 da opa interacting 3 oip 2 tumor p58 pk2 332164775 np_001193725.1 p14618 nm_001206796.2 p14786 q53gk4 q96e76 q9bwb5 q9ucv6 q9upf2 a6nfk3 b2r5n8 b3kry0 b4dfx8 b4duu6 m23725 mrna samples serum plasma tissue homogenates other biological fluids type quantitative sandwich range 0.156 10ng ml 0.061ng intra precision within an with low middle level were tested 20 times on one plate respectively cv protein1 s30 interacting3 oip2 tested20
⇄host => string (48) "E Coli or Yeast or Baculovirus or Mammalian Cell"
$value[8]['_source']['host']
⇄reactivity => string (3) "N/A"
$value[8]['_source']['reactivity']
⇄specificity => string (3) "N/A"
$value[8]['_source']['specificity']
⇄purity => string (57) "Greater or equal to 85% purity as determined by SDS-PAGE."
$value[8]['_source']['purity']
⇄⧉form => string (80) "Lyophilized or liquid (Format to be determined during the manufacturing proc...
$value[8]['_source']['form']
Lyophilized or liquid (Format to be determined during the manufacturing process)
⇄concentration => string (3) "N/A"
$value[8]['_source']['concentration']
⇄⧉storage_stability => string (195) "Store at -20 degrees C. For long-term storage, store at -20 degrees C or -80...
$value[8]['_source']['storage_stability']
Store at -20 degrees C. For long-term storage, store at -20 degrees C or -80 degrees C. Store working aliquots at 4 degrees C for up to one week. Repeated freezing and thawing is not recommended.
SDS-PAGE||Human CLIP-associating protein 2(CLASP2) ,partial <br>His-tagged <br>Yeast derived||AAA18663_SDS_PAGE3.jpg!!SDS-PAGE||Human CLIP-associating protein 2(CLASP2) ,partial<br>His-tagged<br>Mammalian cell derived||AAA18663_SDS_PAGE2.jpg!!SDS-PAGE||Human CLIP-associating protein 2 (CLASP2) ,partial<br>His tag and fused with a sepecial protein<br>E.coli derived||AAA18663_SDS_PAGE.jpg
⇄etc_term1 => string (14) "Species||Human"
$value[8]['_source']['etc_term1']
⇄etc_term2 => string (3) "N/A"
$value[8]['_source']['etc_term2']
⇄products_price => string (6) "0.0000"
$value[8]['_source']['products_price']
⇄products_weight => string (4) "5.00"
$value[8]['_source']['products_weight']
⇄products_status => boolean true
$value[8]['_source']['products_status']
⇄products_tax_class_id => string (1) "1"
$value[8]['_source']['products_tax_class_id']
⇄manufacturers_id => string (3) "700"
$value[8]['_source']['manufacturers_id']
⇄products_ordered => string (1) "0"
$value[8]['_source']['products_ordered']
⇄language_id => string (1) "1"
$value[8]['_source']['language_id']
⇄products_name => string (35) "CLIP-associating protein 2 (CLASP2)"
$value[8]['_source']['products_name']
⇄products_name_oem => string (63) "Recombinant Human CLIP-associating protein 2 (CLASP2) , partial"
⇄⧉search_terms => string (536) "aaa18663 e coli or yeast baculovirus mammalian cell greater equal to 85 puri...
$value[8]['_source']['search_terms']
aaa18663 e coli or yeast baculovirus mammalian cell greater equal to 85 purity as determined by sds page lyophilized liquid format be during the manufacturing process human clip associating protein 2 clasp2 partial his tag and fused with a sepecial e.coli derived aaa18663_sdse tagged aaa18663_sdsm aaa18663_sdsy recombinant isoform cytoplasmic linker associated 165,924 da orbit homolog horbit2 kiaa0627 333440451 np_001193973.1 o75122 nm_001207044.1 q7l8f6 q8n6r6 q9bqt3 q9bqt4 q9h7a3 q9nsz2 b2rtr1 f5h604 605853 species to85 protein2
⇄⧉specificity => string (169) "This assay has high sensitivity and excellent specificity for detection of A...
$value[9]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of Ace2. No significant cross-reactivity or interference between Ace2 and analogues was observed.
⇄purity => string (3) "N/A"
$value[9]['_source']['purity']
⇄form => string (3) "N/A"
$value[9]['_source']['form']
⇄concentration => string (3) "N/A"
$value[9]['_source']['concentration']
⇄⧉storage_stability => string (156) "Store entire kit at 2-8C for short-term. For longer-term, please store the m...
$value[9]['_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
⇄⧉products_description => string (825) "Principle of the Assay: This kit was based on sandwich enzyme-linked immune-...
$value[9]['_source']['products_description']
Principle of the Assay: This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Capture antibody was pre-coated onto 96-well plates. And the biotin conjugated antibody was used as detection antibodies. The standards, test samples and biotin conjugated detection antibody were added to the wells subsequently, and washed with wash buffer. HRP-Streptavidin was added and unbound conjugates were washed away with wash buffer. TMB substrates were used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the target amount of sample captured in plate. Read the O.D. absorbance at 450nm in a microplate reader, and then the concentration of target can be calculated.
⇄⧉ncbi_pathways => string (359) "ACE Inhibitor Pathway||198763!!Metabolism Of Angiotensinogen To Angiotensins...
$value[9]['_source']['ncbi_pathways']
ACE Inhibitor Pathway||198763!!Metabolism Of Angiotensinogen To Angiotensins Pathway||1268749!!Metabolism Of Proteins Pathway||1268677!!Peptide Hormone Metabolism Pathway||1268746!!Protein Digestion And Absorption Pathway||172847!!Protein Digestion And Absorption Pathway||171868!!Renin-angiotensin System Pathway||83075!!Renin-angiotensin System Pathway||486
⇄⧉search_terms => string (569) "aaa17616 rat this assay has high sensitivity and excellent specificity for d...
$value[9]['_source']['search_terms']
aaa17616 rat this assay has high sensitivity and excellent specificity for detection of ace2 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa17616_sc elisa kit angiotensin converting enzyme 2 ace related carboxypeptidase i aceh 63,912 da homolog ace2_human 11225609 np_068576.1 q9byf1 nm_021804.2 q6uwp0 q86wt0 q9nra7 q9ufz6 c7ecu1 300335 samples serum plasma tissue homogenates other biological fluids type quantitative sandwich range 0.625 40ng ml 0.375ng intra precision cv enzyme2
⇄⧉products_description => string (822) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[10]['_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 T3 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"
$value[10]['_source']['products_references']
⇄⧉products_related_diseases => string (191) "Cardiovascular Diseases||19!!Thyroid Diseases||19!!Nervous System Diseases||...
⇄⧉search_terms => string (614) "aaa12487 rat typical testing data standard curve for reference only aaa12487...
$value[10]['_source']['search_terms']
aaa12487 rat typical testing data standard curve for reference only aaa12487_sc elisa kit triiodothyronine t3 thyroid hormone receptor alpha isoform 2 thra ar7 ear7 erba chng6 erba1 nr1a1 thra1 thra2 erb t 1 c ear 7 related v protein nuclear subfamily group a member normone variant erythroblastic leukemia viral oncogene homolog avian 50,465 da tha_human 300116309 np_001177848.1 p10827 nm_001190919.1 p21205 q8n6a1 q96h73 a8k3b5 gene 614450 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 10 ng ml 0.156 sensitivity up to 0.05 intra precision isoform2 t1 range10
⇄⧉specificity => string (183) "This assay has high sensitivity and excellent specificity for detection of h...
$value[11]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of human BIRC2. No significant cross-reactivity or interference between human BIRC2 and analogues was observed.
⇄purity => string (3) "N/A"
$value[11]['_source']['purity']
⇄form => string (3) "N/A"
$value[11]['_source']['form']
⇄concentration => string (3) "N/A"
$value[11]['_source']['concentration']
⇄⧉storage_stability => string (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[11]['_source']['storage_stability']
Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please refer to pdf manual for further storage instructions.
⇄⧉etc_term2 => string (326) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV...
$value[11]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV%<8%. Three samples of known concentration were tested twenty times on one plate to assess!!Inter-assay Precision||Inter-assay Precision (Precision between assays): CV%<10%. Three samples of known concentration were tested in twenty assays to assess.
⇄⧉products_description => string (735) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value[11]['_source']['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for BIRC2 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any BIRC2 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for BIRC2 is added to the wells. After washing, avidin 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 BIRC2 bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄⧉search_terms => string (692) "aaa18402 human this assay has high sensitivity and excellent specificity for...
$value[11]['_source']['search_terms']
aaa18402 human this assay has high sensitivity and excellent specificity for detection of birc2 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa18402_td elisa kit baculoviral iap repeat containing 2 protein api1 hiap2 hiap mihb rnf48 c iap1 ciap1 nfr2 traf signalling complex apoptosis inhibitor 1 isoform homolog b ring finger 48 tnfr2 signaling 69,900 da iap2 birc2_human 4502141 np_001157.1 q13490 nm_001166.4 q16516 q4ttg0 b4e026 601712 samples serum plasma tissue homogenates cell lysates type quantitative sandwich range 23.5 pg ml 1500 5.8 intra precision within an cv containing2 inhibitor1 finger48
⇄⧉specificity => string (179) "This assay has high sensitivity and excellent specificity for detection of m...
$value[12]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of mouse EN2. No significant cross-reactivity or interference between mouse EN2 and analogues was observed.
⇄purity => string (3) "N/A"
$value[12]['_source']['purity']
⇄form => string (3) "N/A"
$value[12]['_source']['form']
⇄concentration => string (3) "N/A"
$value[12]['_source']['concentration']
⇄⧉storage_stability => string (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[12]['_source']['storage_stability']
Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please refer to pdf manual for further storage instructions.
Samples||Serum, plasma, tissue homogenates, cell lysates!!Assay Type||Quantitative Sandwich!!Detection Range||0.312 ng/ml -20 ng/ml!!Sensitivity||Typically less than 0.078 ng/ml.
⇄⧉etc_term2 => string (326) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV...
$value[12]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV%<8%. Three samples of known concentration were tested twenty times on one plate to assess!!Inter-assay Precision||Inter-assay Precision (Precision between assays): CV%<10%. Three samples of known concentration were tested in twenty assays to assess.
Human Homeobox protein engrailed-2 (EN2) ELISA kit; engrailed homolog 2; engrailed-2; engrailed homeobox 2
⇄products_gene_name => string (3) "EN2"
$value[12]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[12]['_source']['products_gene_name_syn']
⇄⧉products_description => string (727) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value[12]['_source']['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for EN2 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any EN2 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for EN2 is added to the wells. After washing, avidin 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 EN2 bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄products_references => string (3) "N/A"
$value[12]['_source']['products_references']
⇄⧉products_related_diseases => string (242) "Nervous System Diseases||29!!Autistic Disorder||20!!Congenital Abnormalities...
⇄⧉search_terms => string (553) "aaa15853 human this assay has high sensitivity and excellent specificity for...
$value[12]['_source']['search_terms']
aaa15853 human this assay has high sensitivity and excellent specificity for detection of mouse en2 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa15853_td elisa kit engrailed homeobox 2 protein homolog hu en 34,211 da hme2_human 7710121 np_001418.2 p19622 nm_001427.3 q549u3 q9ud58 a4d252 131310 samples serum plasma tissue homogenates cell lysates type quantitative sandwich range 0.312 ng ml 20 typically less than 0.078 intra precision within an cv homeobox2 ml20
⇄⧉products_description => string (676) "Principle of the Assay: This experiment use double-sandwich elisa technique ...
$value[13]['_source']['products_description']
Principle of the Assay: This experiment use double-sandwich elisa technique and the ELISA Kit provided is typical. The pre-coated antibody is Human Slit2 monoclonal antibody and the detecting antibody is polyclonal antibody with biotin labeled. Samples and biotin labeling antibody are added into ELISA plate wells and washed out with PBS or TBS. Then Avidin-peroxidase conjugates are added to ELISA wells in order; Use TMB substrate for coloring after reactant thoroughly washed out by PBS or TBS. TMB turns into blue in peroxidase catalytic and finally turns into yellow under the action of acid. The color depth and the testing factors in samples are positively correlated.
⇄⧉search_terms => string (408) "aaa13152 human no cross reaction with other factors typical testing data sta...
$value[13]['_source']['search_terms']
aaa13152 human no cross reaction with other factors typical testing data standard curve for reference only aaa13152_sc elisa kit slit homolog 2 slit2 protein drosophila 169,887 da k7av78_pantr 410353075 jaa43141.1 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 10 ng ml 0.156 sensitivity up to 0.05 intra precision <= 8 inter 12 homolog2 range10 <=8 inter12
⇄⧉specificity => string (183) "This assay has high sensitivity and excellent specificity for detection of h...
$value[14]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of human sEPCR. No significant cross-reactivity or interference between human sEPCR 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 (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[14]['_source']['storage_stability']
Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please refer to pdf manual for further storage instructions.
⇄⧉etc_term2 => string (326) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV...
$value[14]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV%<8%. Three samples of known concentration were tested twenty times on one plate to assess!!Inter-assay Precision||Inter-assay Precision (Precision between assays): CV%<10%. Three samples of known concentration were tested in twenty assays to assess.
⇄⧉products_description => string (735) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value[14]['_source']['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for sEPCR has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any sEPCR present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for sEPCR is added to the wells. After washing, avidin 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 sEPCR bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄⧉search_terms => string (669) "aaa18258 human this assay has high sensitivity and excellent specificity for...
$value[14]['_source']['search_terms']
aaa18258 human this assay has high sensitivity and excellent specificity for detection of sepcr no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa18258_td elisa kit septin 2 sept2 diff6 kiaa0158 nedd5 pnutl3 hnedd5 otthump00000200251 neural precursor cell expressed developmentally down regulated 5 isoform a nedd protein 41,487 da sept2_human 56549636 np_001008491.1 q15019 nm_001008491.2 q14132 q53qu3 q8iuk9 q96cb0 b4dge8 601506 samples serum plasma tissue homogenates type quantitative sandwich range 7.8 ng ml 500 1.95 intra precision within an cv septin2 regulated5 range7.8 ml500
<b>Storage:</b><br>Avoid repeated freeze/thaw cycles.<br>Store at 4 degree C for frequent use.<br>Aliquot and store at -20 degree C for 24 months.<br><br><b>Stability Test:</b><br>thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37 degree C for 48h, and no obvious degradation and precipitation were observed. The loss rate is less than 5% within the expiration date under appropriate storage condition.
Western blotting: 0.5-3ug/mL;<br>Immunohistochemistry: 5-30ug/mL;<br>Immunocytochemistry: 5-30ug/mL;<br>Optimal working dilutions must be determined by end user.
⇄⧉testing_protocols => string (1268) "IHC (Immunohistchemistry)||DAB staining on IHC-P;<br>Samples: Human Kidney T...
$value[15]['_source']['testing_protocols']
IHC (Immunohistchemistry)||DAB staining on IHC-P;<br>Samples: Human Kidney Tissue;<br>Primary Ab: 30ug/ml Rabbit Anti-Human MIB2 Antibody<br>Second Ab: 2ug/mL HRP-Linked Caprine Anti-Rabbit IgG Polyclonal Antibody||AAA20152_IHC6.png!!IHC (Immunohistochemistry)||DAB staining on IHC-P;<br>Samples: Human Lung cancer Tissue;<br>Primary Ab: 30ug/ml Rabbit Anti-Human MIB2 Antibody<br>Second Ab: 2ug/mL HRP-Linked Caprine Anti-Rabbit IgG Polyclonal Antibody||AAA20152_IHC5.png!!IHC (Immunohistochemistry)||DAB staining on IHC-P;<br>Samples: Human Liver cancer Tissue;<br>Primary Ab: 30ug/ml Rabbit Anti-Human MIB2 Antibody<br>Second Ab: 2ug/mL HRP-Linked Caprine Anti-Rabbit IgG Polyclonal Antibody||AAA20152_IHC4.png!!IHC (Immunohistochemistry)||DAB staining on IHC-P;<br>Samples: Human Cerebrum Tissue;<br>Primary Ab: 30ug/ml Rabbit Anti-Human MIB2 Antibody<br>Second Ab: 2ug/mL HRP-Linked Caprine Anti-Rabbit IgG Polyclonal Antibody||AAA20152_IHC3.png!!IHC (Immunohistochemistry)||DAB staining on IHC-P;<br>Samples: Human Liver Tissue;<br>Primary Ab: 30ug/ml Rabbit Anti-Human MIB2 Antibody<br>Second Ab: 2ug/mL HRP-Linked Caprine Anti-Rabbit IgG Polyclonal Antibody||AAA20152_IHC2.jpg!!WB (Western Blot)||Western Blot: Sample: Recombinant MIB2, Human.||AAA20152_WB.jpg
⇄⧉ncbi_pathways => string (174) "Activated NOTCH1 Transmits Signal To The Nucleus Pathway||576270!!Signal Tra...
$value[15]['_source']['ncbi_pathways']
Activated NOTCH1 Transmits Signal To The Nucleus Pathway||576270!!Signal Transduction Pathway||477114!!Signaling By NOTCH Pathway||106485!!Signaling By NOTCH1 Pathway||576269
⇄⧉specificity => string (181) "This assay has high sensitivity and excellent specificity for detection of h...
$value[16]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of human LIPA. No significant cross-reactivity or interference between human LIPA and analogues was observed.
⇄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 (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[16]['_source']['storage_stability']
Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please refer to pdf manual for further storage instructions.
⇄⧉etc_term2 => string (326) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV...
$value[16]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV%<8%. Three samples of known concentration were tested twenty times on one plate to assess!!Inter-assay Precision||Inter-assay Precision (Precision between assays): CV%<10%. Three samples of known concentration were tested in twenty assays to assess.
⇄⧉products_description => string (731) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value[16]['_source']['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for LIPA has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any LIPA present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for LIPA is added to the wells. After washing, avidin 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 LIPA bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄⧉search_terms => string (563) "aaa18045 human this assay has high sensitivity and excellent specificity for...
$value[16]['_source']['search_terms']
aaa18045 human this assay has high sensitivity and excellent specificity for detection of lipa no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa18045_td elisa kit lysyl oxidase like 2 homolog loxl2 lor2 ws9 14 related protein delta e13 86,725 da loxl2_human 4505011 np_002309.1 q9y4k0 nm_002318.2 q53hv3 q9bw70 q9y5y8 b2r5q0 606663 samples serum plasma tissue homogenates cell lysates type quantitative sandwich range 62.5 pg ml 4000 15.6 intra precision within an cv like2 ws914
⇄⧉specificity => string (197) "This assay has high sensitivity and excellent specificity for detection of h...
$value[17]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of human SIRT1/SIR2L1. No significant cross-reactivity or interference between human SIRT1/SIR2L1 and analogues was observed.
⇄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 (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[17]['_source']['storage_stability']
Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please refer to pdf manual for further storage instructions.
⇄⧉etc_term2 => string (327) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV...
$value[17]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV%<8%. Three samples of known concentration were tested twenty times on one plate to assess.!!Inter-assay Precision||Inter-assay Precision (Precision between assays): CV%<10%. Three samples of known concentration were tested in twenty assays to assess.
⇄products_price => string (6) "0.0000"
$value[17]['_source']['products_price']
⇄products_weight => string (4) "5.00"
$value[17]['_source']['products_weight']
⇄products_status => boolean true
$value[17]['_source']['products_status']
⇄products_tax_class_id => string (1) "1"
$value[17]['_source']['products_tax_class_id']
⇄manufacturers_id => string (3) "700"
$value[17]['_source']['manufacturers_id']
⇄products_ordered => string (1) "0"
$value[17]['_source']['products_ordered']
⇄language_id => string (1) "1"
$value[17]['_source']['language_id']
⇄⧉products_name => string (79) "sirtuin (silent mating type information regulation 2 homolog) 1 (S. cerevisi...
$value[17]['_source']['products_name']
sirtuin (silent mating type information regulation 2 homolog) 1 (S. cerevisiae)
Human NAD-dependent deacetylase sirtuin-1 (SIRT1/SIR2L1) ELISA kit; RP11-57G10.3; SIR2L1; SIR2alpha; sir2-like 1; sirtuin 1; sirtuin type 1; sirtuin (silent mating type information regulation 2 homolog) 1 (S. cerevisiae)
⇄products_gene_name => string (5) "SIRT1"
$value[17]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[17]['_source']['products_gene_name_syn']
⇄⧉products_description => string (763) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value[17]['_source']['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for SIRT1/SIR2L1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any SIRT1/SIR2L1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for SIRT1/SIR2L1 is added to the wells. After washing, avidin 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 SIRT1/SIR2L1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄⧉search_terms => string (711) "aaa15752 human this assay has high sensitivity and excellent specificity for...
$value[17]['_source']['search_terms']
aaa15752 human this assay has high sensitivity and excellent specificity for detection of sirt1 sir2l1 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa15752_td elisa kit sirtuin silent mating type information regulation 2 homolog 1 s cerevisiae nad dependent deacetylase rp11 57g10.3 sir2alpha sir2 like protein isoform b hsir2 hsirt1 regulatory 81,681 da 75sirt1 sir1_human 215982798 np_001135970.1 q96eb6 nm_001142498.1 q2xnf6 q5jvq0 q9gzr9 q9y6f0 604479 samples serum plasma cell culture supernates tissue homogenates quantitative sandwich range 0.156 ng ml 10 < 0.039 intra precision within an cv regulation2 homolog1 ml10
⇄⧉specificity => string (386) "This assay has high sensitivity and excellent specificity for detection of E...
$value[18]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of EGFR2ED. No significant cross-reactivity or interference between EGFR2ED and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between EGFR2ED 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."
Assay Type||Quantitative Competitive or Sandwich!!Samples||Serum, plasma, cell culture supernatants, body fluid and tissue homogenate!!Sensitivity||1.0 ng/mL
⇄⧉products_description => string (1533) "Principle of the Assay: EGFR2ED ELISA kit applies the quantitative sandwich ...
$value[18]['_source']['products_description']
Principle of the Assay: EGFR2ED ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for EGFR2ED. Standards or samples are then added to the microtiter plate wells and EGFR2ED if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of EGFR2ED present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for EGFR2ED are added to each well to "sandwich" the EGFR2ED 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 EGFR2ED 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 EGFR2ED concentration in each sample is interpolated from this standard curve.<br><br>Intended Uses: This EGFR2ED ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human EGFR2ED. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
⇄⧉search_terms => string (972) "aaa16347 human this assay has high sensitivity and excellent specificity for...
$value[18]['_source']['search_terms']
aaa16347 human this assay has high sensitivity and excellent specificity for detection of egfr2ed 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 aaa16347_sc elisa kit epidermal growth factor receptor 2 extracellular domain her ecd tyrosine protein kinase erbb isoform a v erb b2 avian erythroblastic leukemia viral oncogene homolog erbb2 neu ngl her2 tkr1 cd340 mln 19 herstatin p185erbb2 proto c metastatic lymph node gene neuro glioblastoma derived type cell surface neuroblastoma oncoprotein 97,253 da cd_antigen mln19 erbb2_human 54792096 np_004439.2 p04626 nm_004448.3 q14256 q6ldv1 q9umk4 b2rzg3 b4dhn3 x5d2v5 613659 samples serum plasma culture supernatants body fluid tissue homogenate quantitative competitive sandwich 1.0 ng ml receptor2 sandwich1.0
⇄⧉specificity => string (167) "This assay has high sensitivity and excellent specificity for detection of E...
$value[19]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of EN2. No significant cross-reactivity or interference between EN2 and analogues was observed.
⇄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 (156) "Store entire kit at 2-8C for short-term. For longer-term, please store the m...
$value[19]['_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
EN2 (Homeobox protein engrailed-2)/AUTS10/engrailed homeobox 2/engrailed homolog 2/engrailed-2/Homeobox protein en-2/hu-En-2/Hu-En-2
⇄products_gene_name => string (3) "EN2"
$value[19]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[19]['_source']['products_gene_name_syn']
⇄⧉products_description => string (825) "Principle of the Assay: This kit was based on sandwich enzyme-linked immune-...
$value[19]['_source']['products_description']
Principle of the Assay: This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Capture antibody was pre-coated onto 96-well plates. And the biotin conjugated antibody was used as detection antibodies. The standards, test samples and biotin conjugated detection antibody were added to the wells subsequently, and washed with wash buffer. HRP-Streptavidin was added and unbound conjugates were washed away with wash buffer. TMB substrates were used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the target amount of sample captured in plate. Read the O.D. absorbance at 450nm in a microplate reader, and then the concentration of target can be calculated.
⇄products_references => string (3) "N/A"
$value[19]['_source']['products_references']
⇄⧉products_related_diseases => string (250) "Nervous System Diseases||33!!Autistic Disorder||22!!Death||17!!Brain Disease...
⇄⧉search_terms => string (623) "aaa17565 human this assay has high sensitivity and excellent specificity for...
$value[19]['_source']['search_terms']
aaa17565 human this assay has high sensitivity and excellent specificity for detection of en2 no significant cross reactivity or interference between analogues was observed note limited by current skills knowledge it is difficult us to complete the crossreactivity all therefore reaction may still exist typical testing data standard curve reference only aaa17565_td elisa kit homeobox protein engrailed 2 auts10 homolog en hu 34,211 da hme2_human 7710121 np_001418.2 p19622 nm_001427.3 q549u3 q9ud58 a4d252 131310 samples serum plasma tissue homogenates other biological fluids type sandwich range 0.312 20ng ml engrailed2
