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` = '18022'
AND `pd`.`language_id` = 1
LIMIT 1
Query
Database
1.69 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 = '18022' and pd.language_id = 1
Query
Database
1.70 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` = '18022'
Database (4 total Queries, 4 of them unique across 2 Connections)
Time
Query String
2.03 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` = '18022'
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 = '18022' 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` = '18022'
⇄⧉specificity => string (183) "This assay has high sensitivity and excellent specificity for detection of h...
$value['specificity']
This assay has high sensitivity and excellent specificity for detection of human SFRP2. No significant cross-reactivity or interference between human SFRP2 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 (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value['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, cell culture supernates, tissue homogenates, cell lysates.!!Detection Range||0.156 ng/ml -10 ng/ml. !!Sensitivity||The minimum detectable dose of human SFRP2 is typically less than 0.039 ng/ml.The sensitivity of this assay, or Lower Limit of Detection (LLD) was defined as the lowest protein concentration that could be differentiated from zero. It was determined the mean O.D value of 20 replicates of the zero standard added by their three standard deviations.!!Assay Type||Sandwich
⇄⧉etc_term2 => string (327) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV...
$value['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 Secreted frizzled-related protein 2 (SFRP2) ELISA kit; FRP-2; SARP1; SDF-5; secreted apoptosis related protein 1; secreted frizzled-related protein 2
⇄products_gene_name => string (5) "SFRP2"
$value['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value['products_gene_name_syn']
⇄⧉products_description => string (735) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for SFRP2 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any SFRP2 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for SFRP2 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 SFRP2 bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄⧉specificity => string (183) "This assay has high sensitivity and excellent specificity for detection of h...
$value->a['specificity']
This assay has high sensitivity and excellent specificity for detection of human SFRP2. No significant cross-reactivity or interference between human SFRP2 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 (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value->a['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, cell culture supernates, tissue homogenates, cell lysates.!!Detection Range||0.156 ng/ml -10 ng/ml. !!Sensitivity||The minimum detectable dose of human SFRP2 is typically less than 0.039 ng/ml.The sensitivity of this assay, or Lower Limit of Detection (LLD) was defined as the lowest protein concentration that could be differentiated from zero. It was determined the mean O.D value of 20 replicates of the zero standard added by their three standard deviations.!!Assay Type||Sandwich
⇄⧉etc_term2 => string (327) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV...
$value->a['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 Secreted frizzled-related protein 2 (SFRP2) ELISA kit; FRP-2; SARP1; SDF-5; secreted apoptosis related protein 1; secreted frizzled-related protein 2
⇄products_gene_name => string (5) "SFRP2"
$value->a['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value->a['products_gene_name_syn']
⇄⧉products_description => string (735) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value->a['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for SFRP2 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any SFRP2 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for SFRP2 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 SFRP2 bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄⧉specificity => string (183) "This assay has high sensitivity and excellent specificity for detection of h...
$value->d['specificity']
This assay has high sensitivity and excellent specificity for detection of human SFRP2. No significant cross-reactivity or interference between human SFRP2 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 (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value->d['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, cell culture supernates, tissue homogenates, cell lysates.!!Detection Range||0.156 ng/ml -10 ng/ml. !!Sensitivity||The minimum detectable dose of human SFRP2 is typically less than 0.039 ng/ml.The sensitivity of this assay, or Lower Limit of Detection (LLD) was defined as the lowest protein concentration that could be differentiated from zero. It was determined the mean O.D value of 20 replicates of the zero standard added by their three standard deviations.!!Assay Type||Sandwich
⇄⧉etc_term2 => string (327) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV...
$value->d['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 Secreted frizzled-related protein 2 (SFRP2) ELISA kit; FRP-2; SARP1; SDF-5; secreted apoptosis related protein 1; secreted frizzled-related protein 2
⇄products_gene_name => string (5) "SFRP2"
$value->d['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value->d['products_gene_name_syn']
⇄⧉products_description => string (735) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value->d['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for SFRP2 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any SFRP2 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for SFRP2 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 SFRP2 bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄products_name => string (59) "Receptor Activator Of Nuclear Factor Kappa B Ligand (RANkL)"
$value[0]['_source']['products_name']
⇄products_name_oem => string (73) "Rat Receptor Activator Of Nuclear Factor Kappa B Ligand (RANkL) ELISA Kit"
$value[0]['_source']['products_name_oem']
⇄products_name_syn => string (3) "N/A"
$value[0]['_source']['products_name_syn']
⇄products_gene_name => string (5) "RANkL"
$value[0]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[0]['_source']['products_gene_name_syn']
⇄⧉products_description => string (825) "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 RANkL 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.
Necrosis||1448!!Osteoporosis||962!!Neoplasms||828!!Inflammation||446!!Osteolysis||306!!Cardiovascular Diseases||282!!Breast Neoplasms||206!!Alveolar Bone Loss||131!!Osteopetrosis||112!!Pain||105
⇄⧉search_terms => string (646) "aaa13067 rat typical testing data standard curve for reference only aaa13067...
$value[0]['_source']['search_terms']
aaa13067 rat typical testing data standard curve for reference only aaa13067_sc elisa kit receptor activator of nuclear factor kappa b ligand rankl tumor necrosis superfamily member 11 tnfsf11 odf opgl sodf cd254 optb2 trance hrankl2 osteoprotegerin osteoclast differentiation tnf related activation induced cytokine 30,523 da cd_antigen cd254cleaved into the following 2 chains:tumor membrane form soluble tnf11_human 2612922 aab86811.1 o14788 o14723 q96q17 q9p2q3 602642 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 1000 pg ml 15.6 sensitivity up to 5 intra precision member11 following2 to5
⇄products_name => string (59) "Receptor Activator Of Nuclear Factor Kappa B Ligand (RANkL)"
$value[1]['_source']['products_name']
⇄products_name_oem => string (76) "Rabbit Receptor Activator Of Nuclear Factor Kappa B Ligand (RANkL) ELISA Kit"
$value[1]['_source']['products_name_oem']
⇄products_name_syn => string (3) "N/A"
$value[1]['_source']['products_name_syn']
⇄products_gene_name => string (5) "RANkL"
$value[1]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[1]['_source']['products_gene_name_syn']
⇄⧉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-Rabbit RANkL 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 (688) "aaa22441 rabbit no cross reaction with other factors typical testing data st...
$value[1]['_source']['search_terms']
aaa22441 rabbit no cross reaction with other factors typical testing data standard curve for reference only aaa22441_sc elisa kit receptor activator of nuclear factor kappa b ligand rankl tumor necrosis superfamily member 11 tnfsf11 odf opgl sodf cd254 optb2 trance hrankl2 osteoprotegerin osteoclast differentiation tnf related activation induced cytokine 30,523 da cd_antigen cd254cleaved into the following 2 chains:tumor membrane form soluble tnf11_human 2612922 aab86811.1 o14788 o14723 q96q17 q9p2q3 602642 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 2000 pg ml 31.2 sensitivity up to 12 intra precision member11 following2 to12
⇄⧉etc_term1 => string (213) "Samples||Human Serum, Plasma Or Cell Culture Supernatant And Organizations I...
$value[2]['_source']['etc_term1']
Samples||Human Serum, Plasma Or Cell Culture Supernatant And Organizations In The Natural And Recombinant Rab11B Concentration!!Assay Type||Sandwich!!Detection Range||20 ng/ml-0.312 ng/ml!!Sensitivity||0.06 ng/ml.
⇄products_name => string (59) "Receptor Activator Of Nuclear Factor Kappa B Ligand (RANkL)"
$value[2]['_source']['products_name']
⇄products_name_oem => string (75) "Human Receptor Activator Of Nuclear Factor Kappa B Ligand (RANkL) ELISA Kit"
$value[2]['_source']['products_name_oem']
⇄products_name_syn => string (3) "N/A"
$value[2]['_source']['products_name_syn']
⇄products_gene_name => string (5) "RANkL"
$value[2]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[2]['_source']['products_gene_name_syn']
⇄⧉products_description => string (677) "Principle of the Assay: This experiment use double-sandwich elisa technique ...
$value[2]['_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 RAB11B 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.
Necrosis||1448!!Osteoporosis||962!!Neoplasms||828!!Inflammation||446!!Osteolysis||306!!Cardiovascular Diseases||282!!Breast Neoplasms||206!!Alveolar Bone Loss||131!!Osteopetrosis||112!!Pain||105
⇄⧉search_terms => string (734) "aaa13036 human no cross reaction with other factors typical testing data sta...
$value[2]['_source']['search_terms']
aaa13036 human no cross reaction with other factors typical testing data standard curve for reference only aaa13036_sc elisa kit receptor activator of nuclear factor kappa b ligand rankl tumor necrosis superfamily member 11 tnfsf11 odf opgl sodf cd254 optb2 trance hrankl2 osteoprotegerin osteoclast differentiation tnf related activation induced cytokine 30,523 da cd_antigen cd254cleaved into the following 2 chains:tumor membrane form soluble tnf11_human 2612922 aab86811.1 o14788 o14723 q96q17 q9p2q3 602642 samples serum plasma or cell culture supernatant and organizations in natural recombinant rab11b concentration assay type sandwich detection range 20 ng ml 0.312 sensitivity 0.06 intra precision member11 following2 range20
⇄⧉etc_term1 => string (173) "Samples||Serum, plasma, Cell Culture Supernatants, body fluid and tissue hom...
$value[3]['_source']['etc_term1']
Samples||Serum, plasma, Cell Culture Supernatants, body fluid and tissue homogenate!!Assay Type||Competitive or Sandwich!!Detection Range||0.5-10ng/mL!!Sensitivity||0.1ng/ml
⇄⧉products_description => string (1463) "Intended Uses: This RANKL ELISA kit is a 1.5 hour solid-phase ELISA designed...
$value[3]['_source']['products_description']
Intended Uses: This RANKL ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Rat RANKL. This ELISA kit for research use only!<br><br>Principle of the Assay: RANKL ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for RANKL. Standards or samples are then added to the microtiter plate wells and RANKL if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of RANKL present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for RANKL are added to each well to "sandwich" the RANKL 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 RANKL 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 RANKL concentration in each sample is interpolated from this standard curve.
⇄⧉search_terms => string (676) "aaa16274 rat typical testing data standard curve for reference only aaa16274...
$value[3]['_source']['search_terms']
aaa16274 rat typical testing data standard curve for reference only aaa16274_td elisa kit receptor activator of nuclear factor kb ligand rankl tumor necrosis superfamily member 11 tnfsf11 odf opgl sodf cd254 optb2 trance hrankl2 osteoprotegerin osteoclast differentiation tnf related activation induced cytokine kappa b 30,523 da cd_antigen cd254cleaved into the following 2 chains:tumor membrane form soluble tnf11_human 2612922 aab86811.1 o14788 o14723 q96q17 q9p2q3 602642 immunology samples serum plasma cell culture supernatants body fluid and tissue homogenate assay type competitive or sandwich detection range 0.5 10ng ml sensitivity 0.1ng member11 following2 range0.5
⇄⧉etc_term1 => string (173) "Samples||Serum, plasma, Cell Culture Supernatants, body fluid and tissue hom...
$value[4]['_source']['etc_term1']
Samples||Serum, plasma, Cell Culture Supernatants, body fluid and tissue homogenate!!Assay Type||Competitive or Sandwich!!Detection Range||0.5-10ng/mL!!Sensitivity||0.1ng/mL
⇄⧉etc_term2 => string (201) "Intended Uses||This GDF-11 ELISA kit is a 1.5 hour solid-phase ELISA designe...
$value[4]['_source']['etc_term2']
Intended Uses||This GDF-11 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human GDF-11. This ELISA kit for research use only, not for therapeutic applications!
⇄⧉products_description => string (1307) "<b>Principle of the assay: </b>GDF-11 ELISA kit applies the quantitative san...
$value[4]['_source']['products_description']
<b>Principle of the assay: </b>GDF-11 ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for GDF-11. Standards or samples are then added to the microtiter plate wells and GDF-11 if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of GDF-11 present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for GDF-11 are added to each well to "sandwich" the GDF-11 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 GDF-11 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 GDF-11 concentration in each sample is interpolated from this standard curve.
⇄⧉search_terms => string (575) "aaa16512 human typical testing data standard curve for reference only aaa165...
$value[4]['_source']['search_terms']
aaa16512 human typical testing data standard curve for reference only aaa16512_td elisa kit growth differentiation factor 11 gdf11 bmp11 bmp gdf bone morphogenetic protein 45,091 da gdf11_human 5031613 np_005802.1 o95390 nm_005811.3 q9uid1 q9uid2 603936 cancer samples serum plasma cell culture supernatants body fluid and tissue homogenate assay type competitive or sandwich detection range 0.5 10ng ml sensitivity 0.1ng intended uses this is a 1.5 hour solid phase designed the quantitative determination of research use not therapeutic applications! factor11 range0.5 a1.5
⇄⧉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 GDF11. No significant cross-reactivity or interference between human GDF11 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.
Human Growth/differentiation factor 11 (GDF11) ELISA kit; BMP-11; BMP11; bone morphogenetic protein 11; growth differentiation factor 11
⇄products_gene_name => string (5) "GDF11"
$value[5]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[5]['_source']['products_gene_name_syn']
⇄⧉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 GDF11 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any GDF11 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for GDF11 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 GDF11 bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄⧉search_terms => string (543) "aaa18329 human this assay has high sensitivity and excellent specificity for...
$value[5]['_source']['search_terms']
aaa18329 human this assay has high sensitivity and excellent specificity for detection of gdf11 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa18329_td elisa kit growth differentiation factor 11 bmp bmp11 bone morphogenetic protein gdf 45,091 da gdf11_human 5031613 np_005802.1 o95390 nm_005811.3 q9uid1 q9uid2 603936 samples serum plasma tissue homogenates type quantitative sandwich range 28 pg ml 1800 < 7 intra precision within an cv factor11 range28 <7
⇄⧉specificity => string (171) "This assay has high sensitivity and excellent specificity for detection of G...
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This assay has high sensitivity and excellent specificity for detection of GDF15. No significant cross-reactivity or interference between GDF15 and analogues was observed.
⇄purity => string (3) "N/A"
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⇄form => string (3) "N/A"
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⇄⧉storage_stability => string (156) "Store entire kit at 2-8C for short-term. For longer-term, please store the m...
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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
⇄⧉etc_term1 => string (153) "Assay Type||Sandwich!!Samples||Serum, plasma, tissue homogenates and other b...
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Assay Type||Sandwich!!Samples||Serum, plasma, tissue homogenates and other biological fluids!!Detection Range||23.438-1500pg/ml!!Sensitivity||14.063pg/ml
⇄⧉products_description => string (825) "Principle of the Assay: This kit was based on sandwich enzyme-linked immune-...
$value[6]['_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.
⇄⧉search_terms => string (673) "aaa17596 human this assay has high sensitivity and excellent specificity for...
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aaa17596 human this assay has high sensitivity and excellent specificity for detection of gdf15 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa17596_sc elisa kit growth differentiation factor 15 gdf mic 1 mic1 nag pdf plab ptgfb tgf pl 34,140 da macrophage inhibitory cytokine nsaid activated gene protein regulated nrg placental beta bone morphogenetic prostate gdf15_human 14286322 aah08962.1 q99988 o14629 p78360 q9bwa0 q9nrt0 605312 samples serum plasma tissue homogenates other biological fluids type quantitative sandwich range 23.438 1500pg ml 14.063pg intra precision cv factor15
⇄⧉etc_term1 => string (163) "Samples||Serum, plasma, Cell Culture Supernatants, body fluid and tissue hom...
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Samples||Serum, plasma, Cell Culture Supernatants, body fluid and tissue homogenate!!Assay Type||Competitive!!Detection Range||250-5000pg/mL!!Sensitivity||1.0pg/mL
⇄⧉etc_term2 => string (201) "Intended Uses||This GDF-15 ELISA kit is a 1.5 hour solid-phase ELISA designe...
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Intended Uses||This GDF-15 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Mouse GDF-15. This ELISA kit for research use only, not for therapeutic applications!
⇄⧉products_description => string (1199) "<b>Principle of the assay: </b>GDF-15 ELISA kit applies the competitive enzy...
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<b>Principle of the assay: </b>GDF-15 ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-GDF-15 antibody and an GDF-15-HRP conjugate. The assay sample and buffer are incubated together with GDF-15-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 GDF-15 concentration since GDF-15 from samples and GDF-15-HRP conjugate compete for the anti-GDF-15 antibody binding site. Since the number of sites is limited, as more sites are occupied by GDF-15 from the sample, fewer sites are left to bind GDF-15-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The GDF-15 concentration in each sample is interpolated from this standard curve.
⇄⧉search_terms => string (736) "aaa15970 mouse typical testing data standard curve for reference only aaa159...
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aaa15970 mouse typical testing data standard curve for reference only aaa15970_td elisa kit growth differentiation factor 15 gdf15 pdf mic1 plab mic 1 nag ptgfb gdf nrg ptgf beta placental tgf nsaid activated gene protein regulated prostate macrophage inhibitory cytokine bone morphogenetic nonsteroidal anti inflammatory drug 34,140 da gdf15_human 153792495 np_004855.2 q99988 nm_004864.2 o14629 p78360 q9bwa0 q9nrt0 605312 cancer samples serum plasma cell culture supernatants body fluid and tissue homogenate assay type competitive detection range 250 5000pg ml sensitivity 1.0pg intended uses this is a 1.5 hour solid phase designed the quantitative determination of research use not therapeutic applications! factor15 range250 a1.5
⇄⧉products_description => string (677) "Principle of the Assay: This experiment use double-sandwich elisa technique ...
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Principle of the Assay: This experiment use double-sandwich elisa technique and the ELISA Kit provided is typical. The pre-coated antibody is human GDF-15 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 (612) "aaa13116 human no cross reaction with other factors typical testing data sta...
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aaa13116 human no cross reaction with other factors typical testing data standard curve for reference only aaa13116_sc elisa kit growth differentiation factor 15 gdf15 pdf mic1 plab mic 1 nag ptgfb gdf nrg ptgf beta placental tgf nsaid activated gene protein regulated prostate macrophage inhibitory cytokine bone morphogenetic nonsteroidal anti inflammatory drug 34,140 da gdf15_human 14286322 aah08962.1 q99988 o14629 p78360 q9bwa0 q9nrt0 605312 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 2000 pg ml 31.2 sensitivity up to 12 intra precision factor15 to12
⇄⧉specificity => string (181) "This assay has high sensitivity and excellent specificity for detection of h...
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This assay has high sensitivity and excellent specificity for detection of human PRM1. No significant cross-reactivity or interference between human PRM1 and analogues was observed.
⇄purity => string (3) "N/A"
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⇄form => string (3) "N/A"
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⇄concentration => string (3) "N/A"
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⇄⧉storage_stability => string (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
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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!!Assay Type||Quantitative Sandwich!!Detection Range||31.25 pg/ml -2000 pg/ml!!Sensitivity||Typically less than 7.8 pg/ml.
⇄⧉etc_term2 => string (326) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV...
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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 Protamine 1; PRM1 ELISA Kit; CT94.1; P1; cancer/testis antigen family 94; member 1; sperm protamine P1; testis specific protamine 1; protamine 1
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⇄products_gene_name_syn => string (3) "N/A"
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⇄⧉products_description => string (731) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
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Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for PRM1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any PRM1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for PRM1 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 PRM1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄⧉search_terms => string (554) "aaa15384 human this assay has high sensitivity and excellent specificity for...
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aaa15384 human this assay has high sensitivity and excellent specificity for detection of prm1 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa15384_td elisa kit protamine 1 ct94.1 p1 cancer testis antigen family 94 member sperm specific cysteine rich 6,823 da hsp1_human 4506109 np_002752.1 p04553 nm_002761.2 182880 samples serum plasma type quantitative sandwich range 31.25 pg ml 2000 typically less than 7.8 intra precision within an cv protamine1 family94 than7.8
⇄⧉specificity => string (183) "This assay has high sensitivity and excellent specificity for detection of m...
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This assay has high sensitivity and excellent specificity for detection of mouse GDF11. No significant cross-reactivity or interference between mouse GDF11 and analogues was observed.
⇄purity => string (3) "N/A"
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⇄form => string (3) "N/A"
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⇄concentration => string (3) "N/A"
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⇄⧉storage_stability => string (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
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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...
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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.
Mouse Growth/differentiation factor 11 (GDF11) ELISA kit; BMP-11; BMP11; bone morphogenetic protein 11; growth differentiation factor 11
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Principle of the Assay||This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for GDF11 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any GDF11 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for GDF11 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 GDF11 bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄⧉search_terms => string (615) "aaa18327 mouse this assay has high sensitivity and excellent specificity for...
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aaa18327 mouse this assay has high sensitivity and excellent specificity for detection of gdf11 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa18327_td elisa kit growth differentiation factor 11 bmp bmp11 bone morphogenetic protein gdf 44,947 da gdf11_mouse 112807180 np_034402.1 q9z1w4 nm_010272.1 q9qx55 q9r221 samples serum plasma tissue homogenates type sandwich range 18.75 pg ml 1200 4.67 intra precision within an cv <8 three known concentration were tested twenty times on one plate to assess inter assays <10 in factor11
⇄⧉etc_term1 => string (161) "Samples||Serum, plasma, Cell Culture Supernatants, body fluid and tissue hom...
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Samples||Serum, plasma, Cell Culture Supernatants, body fluid and tissue homogenate!!Assay Type||Competitive!!Detection Range||0.5-10ng/mL!!Sensitivity||0.1ng/mL
⇄⧉etc_term2 => string (199) "Intended Uses||This GDF-5 ELISA kit is a 1.5 hour solid-phase ELISA designed...
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Intended Uses||This GDF-5 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human GDF-5. This ELISA kit for research use only, not for therapeutic applications!
⇄⧉products_description => string (1188) "<b>Principle of the assay: </b>GDF-5 ELISA kit applies the competitive enzym...
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<b>Principle of the assay: </b>GDF-5 ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-GDF-5 antibody and an GDF-5-HRP conjugate. The assay sample and buffer are incubated together with GDF-5-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 GDF-5 concentration since GDF-5 from samples and GDF-5-HRP conjugate compete for the anti-GDF-5 antibody binding site. Since the number of sites is limited, as more sites are occupied by GDF-5 from the sample, fewer sites are left to bind GDF-5-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The GDF-5 concentration in each sample is interpolated from this standard curve.
⇄⧉search_terms => string (493) "aaa16419 human typical testing data standard curve for reference only aaa164...
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aaa16419 human typical testing data standard curve for reference only aaa16419_td elisa kit growth differentiation factor 5 gdf5 partial 18,733 da d3yqt0_human 290566063 add39410.1 cancer samples serum plasma cell culture supernatants body fluid and tissue homogenate assay type competitive detection range 0.5 10ng ml sensitivity 0.1ng intended uses this gdf is a 1.5 hour solid phase designed the quantitative determination of research use not therapeutic applications! factor5 range0.5 a1.5
⇄⧉specificity => string (376) "This assay has high sensitivity and excellent specificity for detection of G...
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This assay has high sensitivity and excellent specificity for detection of GDF3. No significant cross-reactivity or interference between GDF3 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between GDF3 and all the analogues, therefore, cross reaction may still exist in some cases.
⇄purity => string (3) "N/A"
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⇄form => string (3) "N/A"
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⇄concentration => string (3) "N/A"
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⇄storage_stability => string (35) "Store all reagents at 2-8 degree C."
⇄⧉products_description => string (1389) "Principle of the Assay: GDF3 ELISA kit applies the competitive enzyme immuno...
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Principle of the Assay: GDF3 ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-GDF3 antibody and an GDF3-HRP conjugate. The assay sample and buffer are incubated together with GDF3-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 GDF3 concentration since GDF3 from samples and GDF3-HRP conjugate compete for the anti-GDF3 antibody binding site. Since the number of sites is limited, as more sites are occupied by GDF3 from the sample, fewer sites are left to bind GDF3-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The GDF3 concentration in each sample is interpolated from this standard curve.<br><br>Intended Uses: This GDF3 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Mouse GDF3. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
⇄products_references => string (3) "N/A"
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⇄⧉products_related_diseases => string (254) "Neoplasms, Germ Cell and Embryonal||15!!Carcinoma||11!!Breast Neoplasms||5!!...
⇄⧉search_terms => string (666) "aaa16075 mouse this assay has high sensitivity and excellent specificity for...
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aaa16075 mouse this assay has high sensitivity and excellent specificity for detection of gdf3 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 aaa16075_sc elisa kit growth differentiation factor 3 kfs3 mcop7 mcopcb6 gdf 41,387 da unq222 pro248 gdf3_human 10190670 np_065685.1 q9nr23 nm_020634.1 q8nej4 613704 cancer samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative competitive 1.0 pg ml factor3 competitive1.0
⇄⧉specificity => string (183) "This assay has high sensitivity and excellent specificity for detection of h...
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This assay has high sensitivity and excellent specificity for detection of human AKAP4. No significant cross-reactivity or interference between human AKAP4 and analogues was observed.
⇄purity => string (3) "N/A"
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⇄form => string (3) "N/A"
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⇄concentration => string (3) "N/A"
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⇄⧉storage_stability => string (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
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Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please refer to pdf manual for further storage instructions.
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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.
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⇄products_name => string (32) "A kinase (PRKA) anchor protein 4"
Human A-kinase anchor protein 4 (AKAP4) ELISA kit; RP13-377G1__B.1; AKAP82; CT99; FSC1; HI; hAKAP82; p82; A-kinase anchor protein 4; A-kinase anchor protein 82 kDa; cancer/testis antigen 99; protein kinase A anchoring protein 4; testis-specific gene HI; A kinase (PRKA) anchor protein 4
⇄products_gene_name => string (5) "AKAP4"
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⇄products_gene_name_syn => string (3) "N/A"
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⇄⧉products_description => string (735) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
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Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for AKAP4 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any AKAP4 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for AKAP4 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 AKAP4 bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄products_references => string (3) "N/A"
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⇄⧉products_related_diseases => string (162) "Genital Diseases, Male||19!!Infertility, Male||16!!Immune System Diseases||2...
A-kinase anchor protein 4; testis-specific gene HI; cancer/testis antigen 99; A-kinase anchor protein 82 kDa; major sperm fibrous sheath protein; protein kinase A anchoring protein 4; protein kinase A-anchoring protein 4
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⇄ncbi_pathways => string (36) "G Protein Signaling Pathways||198849"
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⇄⧉sp_protein_name_syn => string (133) "A-kinase anchor protein 82 kDa; AKAP 82; hAKAP82; Major sperm fibrous sheath...
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A-kinase anchor protein 82 kDa; AKAP 82; hAKAP82; Major sperm fibrous sheath protein; HI; Protein kinase A-anchoring protein 4; PRKA4
⇄⧉search_terms => string (670) "aaa18226 human this assay has high sensitivity and excellent specificity for...
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aaa18226 human this assay has high sensitivity and excellent specificity for detection of akap4 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa18226_td elisa kit a kinase prka anchor protein 4 rp13 377g1__b.1 akap82 ct99 fsc1 hi hakap82 p82 82 kda cancer testis antigen 99 anchoring specific gene isoform 1 prka4 akap major sperm fibrous sheath 94,477 da akap4_human 21493037 np_003877.2 q5jqc9 nm_003886.2 o60904 o95246 q5jqd1 q5jqd2 q5jqd3 a0av85 300185 samples serum plasma tissue homogenates type quantitative sandwich range 25 pg ml 1600 protein4 p8282 antigen99 isoform1 range25
⇄⧉products_description => string (884) "Intended Uses: This sandwich kit is for the accurate quantitative detection ...
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Intended Uses: This sandwich kit is for the accurate quantitative detection of Mouse Growth Differentiation Factor 11 (also known as GDF11) in serum, plasma, cell culture supernates, cell lysates, tissue homogenates.<br><br>Principles of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (ELISA). The plate has been pre-coated with Mouse GDF11 antibody. GDF11 present in the sample is added and binds to antibodies coated on the wells. And then biotinylated Mouse GDF11 Antibody is added and binds to GDF11 in the sample. Then Streptavidin-HRP is added and binds to the Biotinylated GDF11 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 Mouse GDF11. The reaction is terminated by addition of acidic stop solution and absorbance is measured at 450 nm
Assay Type||Quantitative Sandwich!!Samples||Serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids!!Detection Range||15-3000ng/L!!Sensitivity||7.28ng/L
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Intra-assay Precision||Intra-Assay Precision (Precision within an assay) Three samples of known concentration were tested on one plate to assess intra-assay precision. Intra-Assay: CV<8%!!Inter-assay Precision||Inter-Assay Precision (Precision between assays) Three samples of known concentration were tested in separate assays to assess inter-assay precision. CV(%) = SD/mean x 100. Inter-Assay: CV<10%
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⇄⧉products_name => string (89) "Sushi, von Willebrand factor type A, EGF and pentraxin domain-containing pro...
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Sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1, SVEP1
⇄⧉products_name_oem => string (105) "Human Sushi, von Willebrand factor type A, EGF and pentraxin domain-containi...
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Human Sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1, SVEP1 ELISA Kit
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⇄products_gene_name => string (5) "SVEP1"
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⇄products_gene_name_syn => string (3) "N/A"
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⇄⧉products_description => string (956) "Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (EL...
$value[15]['_source']['products_description']
Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (ELISA). The plate has been pre-coated with Human SVEP1 antibody. SVEP1 present in the sample is added and binds to antibodies coated on the wells. And then biotinylated Human SVEP1 Antibody is added and binds to SVEP1 in the sample. Then Streptavidin-HRP is added and binds to the Biotinylated SVEP1 antibody. After incubation unbound Streptavidin-HRP is washed away during a washing step. Substrate solution is then added and color develops in proportion to the amount of Human SVEP1. 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 Human Sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1 (also known as SVEP1) in serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids.
⇄⧉search_terms => string (495) "aaa19084 human elisa kit sushi von willebrand factor type a egf and pentraxi...
$value[15]['_source']['search_terms']
aaa19084 human elisa kit sushi von willebrand factor type a egf and pentraxin domain containing protein 1 svep1 ccp module 22 polydom selectin like osteoblast derived sel ob serologically defined breast cancer antigen ny br 38 c9orf13 ccp22 selob svep1_human 148886654 np_699197.3 q4lde5 611691 assay quantitative sandwich samples serum plasma cell culture supernates lysates tissue homogenates other biological fluids detection range 15 ng l 3000 sensitivity 7.28 protein1 module22 br38 range15
⇄⧉specificity => string (183) "This assay has high sensitivity and excellent specificity for detection of M...
$value[16]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of Mouse GDF15. No significant cross-reactivity or interference between Mouse GDF15 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 (391) "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% is less than 8%<br>Three samples of known concentration were tested twenty times on one plate to assess.<br>Inter-assay Precision (Precision between assays): CV% is less than 10%<br>Three samples of known concentration were tested in twenty assays to assess.!!Detection Wavelength||450 nm!!Sample Volume||50-100ul
⇄⧉products_description => string (742) "<b>Principle of the Assay: </b>This assay employs the quantitative sandwich ...
$value[16]['_source']['products_description']
<b>Principle of the Assay: </b>This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for GDF15 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any GDF15 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for GDF15 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 GDF15 bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄⧉search_terms => string (841) "aaa18194 mouse this assay has high sensitivity and excellent specificity for...
$value[16]['_source']['search_terms']
aaa18194 mouse this assay has high sensitivity and excellent specificity for detection of gdf15 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa18194_td elisa kit growth differentiation factor 15 gdf mic 1 mic1 nag pdf plab ptgfb nsaid nonsteroidal anti inflammatory drug activated protein ptgf beta prostate sbf macrophage inhibiting cytokine 33,225 da gdf15_mouse 170784848 np_035949.2 q9z0j7 nm_011819.2 q6nx63 samples serum plasma cell culture supernates tissue homogenates type sandwich range 7.8 pg ml 500 1.95 intra precision within an cv is less than 8 three known concentration were tested twenty times on one plate to assess inter assays 10 in wavelength 450 nm sample volume 50 100ul factor15 range7.8 ml500 than8 assays10 wavelength450 volume50
⇄⧉specificity => string (173) "This assay has high sensitivity and excellent specificity for detection of I...
$value[17]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of IFITM1. No significant cross-reactivity or interference between IFITM1 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 (156) "Store entire kit at 2-8C for short-term. For longer-term, please store the m...
$value[17]['_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_name_syn => string (80) "9 27; CD225; IFI17; IFITM1; Interferon induced protein 17; Leu 13 antigen; L...
$value[17]['_source']['products_name_syn']
9 27; CD225; IFI17; IFITM1; Interferon induced protein 17; Leu 13 antigen; LEU13
⇄products_gene_name => string (6) "IFITM1"
$value[17]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[17]['_source']['products_gene_name_syn']
⇄⧉products_description => string (825) "Principle of the Assay: This kit was based on sandwich enzyme-linked immune-...
$value[17]['_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.
interferon-induced transmembrane protein 1; leu-13 antigen; interferon-induced protein 17; dispanin subfamily A member 2a; interferon-inducible protein 9-27
Adaptive Immune System Pathway||366160!!B Cell Receptor Signaling Pathway||83081!!B Cell Receptor Signaling Pathway||492!!Cytokine Signaling In Immune System Pathway||366171!!Immune System Pathway||106386!!Immunoregulatory Interactions Between A Lymphoid And A Non-Lymphoid Cell Pathway||106413!!Interferon Signaling Pathway||187103!!Interferon Alpha/beta Signaling Pathway||187104
⇄sp_protein_name => string (42) "Interferon-induced transmembrane protein 1"
$value[17]['_source']['sp_protein_name']
⇄⧉sp_protein_name_syn => string (139) "Dispanin subfamily A member 2a; DSPA2a; Interferon-induced protein 17; Inter...
$value[17]['_source']['sp_protein_name_syn']
Dispanin subfamily A member 2a; DSPA2a; Interferon-induced protein 17; Interferon-inducible protein 9-27; Leu-13 antigen; CD_antigen: CD225
⇄⧉search_terms => string (630) "aaa27624 human this assay has high sensitivity and excellent specificity for...
$value[17]['_source']['search_terms']
aaa27624 human this assay has high sensitivity and excellent specificity for detection of ifitm1 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa27624_sc elisa kit interferon induced transmembrane protein 1 9 27 cd225 ifi17 17 leu 13 antigen leu13 dspa2a dispanin subfamily a member 2a inducible 125 cd_antigen ifm1_human 215274118 p13164.3 p13164 aab25699 q15322 q53xz0 604456 samples serum plasma tissue homogenates other biological fluids type quantitative sandwich range 0.156 10ng ml 0.094ng intra precision cv protein1 ifi1717 inducible125
⇄⧉specificity => string (183) "This assay has high sensitivity and excellent specificity for detection of h...
$value[18]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of human CRYAB. No significant cross-reactivity or interference between human CRYAB and analogues was observed.
⇄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 (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[18]['_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[18]['_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 Alpha-crystallin B chain (CRYAB) ELISA kit; CRYA2; CTPP2; HSPB5; alpha B crystallin; alpha crystallin B chain; heat-shock 20 kD like-protein; crystallin; alpha B
⇄products_gene_name => string (5) "CRYAB"
$value[18]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[18]['_source']['products_gene_name_syn']
⇄⧉products_description => string (735) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value[18]['_source']['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for CRYAB has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any CRYAB present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for CRYAB 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 CRYAB 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[18]['_source']['products_references']
⇄⧉products_related_diseases => string (206) "Nervous System Diseases||46!!Cardiovascular Diseases||38!!Cataract||27!!Eye ...
⇄⧉search_terms => string (734) "aaa18348 human this assay has high sensitivity and excellent specificity for...
$value[18]['_source']['search_terms']
aaa18348 human this assay has high sensitivity and excellent specificity for detection of cryab no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa18348_td elisa kit crystallin alpha b chain crya2 ctpp2 hspb5 heat shock 20 kd like protein mfm2 cmd1ii ctrct16 hel s 101 beta 5 rosenthal fiber component renal carcinoma antigen ny ren 27 epididymis secretory li 20,159 da cryab_human 577019571 np_001276736.1 p02511 nm_001289807.1 o43416 q9uc37 q9uc38 q9uc39 q9uc40 q9uc41 b0yix0 615184 samples serum plasma cell lysates tissue homogenates type quantitative sandwich range 12.5 pg ml 800 < 3.12 intra precision within an cv shock20 s101 beta5 ren27 ml800
⇄products_name => string (23) "Dickkopf-like protein 1"
$value[19]['_source']['products_name']
⇄products_name_oem => string (39) "Human Dickkopf-like protein 1 ELISA Kit"
$value[19]['_source']['products_name_oem']
⇄⧉products_name_syn => string (108) "Dickkopf-like protein 1; Cancer/testis antigen 34; CT34; Protein soggy-1; SG...
$value[19]['_source']['products_name_syn']
Dickkopf-like protein 1; Cancer/testis antigen 34; CT34; Protein soggy-1; SGY-1; DKKL1; SGY1; UNQ735/PRO1429
⇄products_gene_name => string (5) "DKKL1"
$value[19]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[19]['_source']['products_gene_name_syn']
⇄⧉products_description => string (1104) "Intended Uses: This immunoassay kit allows for the in vitro quantitative det...
$value[19]['_source']['products_description']
Intended Uses: This immunoassay kit allows for the in vitro quantitative determination of target antigen concentrations in serum, plasma, tissue homogenates, cell culture supernates 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 target antigen. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for target antigen and then avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. Only those wells that contain target antigen, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 +/- 2 nm. The concentration of target antigen 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[19]['_source']['products_references']
⇄⧉products_related_diseases => string (138) "Infertility, Female||3!!Carcinoma||1!!Nervous System Diseases||1!!Weight Gai...
⇄⧉search_terms => string (483) "aaa23185 human recombinant and natural dickkopf like protein 1 typical testi...
$value[19]['_source']['search_terms']
aaa23185 human recombinant and natural dickkopf like protein 1 typical testing data standard curve for reference only aaa23185_sc elisa kit cancer testis antigen 34 ct34 soggy sgy dkkl1 sgy1 unq735 pro1429 isoform 2 acrosomal 27,007 da dkkl1_human 308818218 np_001184230.1 q9uk85 nm_001197301.1 605418 samples serum plasma tissue homogenates cell culture supernates or other biological fluids detection range 78 5000 pg ml intra assay precision cv protein1 antigen34 isoform2 range78
