Highly validated and characterized monoclonal/polyclonal
antibodies and recombinant
proteins
The majority of AAA Biotech’s antibodies are highly validated and can be use in multiple
applications such as ELISA, FC,
ICC, IF, IHC, IP, WB, etc. We have antibodies available for rare species, in multiple conjugated
forms or recombinant
antibodies.
As for our high quality proteins, the majority have 90% purity, detected by SDS-PAGE while some are
available in
different tags such as Flag, GST, His, MBP, etc. We also carry high quality native and biologically
active proteins.
AAA Biotech is constantly working to expand our capacity to provide recombinant proteins and
antibodies to most
target proteins.
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Database
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ifnull(pdns.ncbi_summary, 'N/A') as ncbi_summary_pdns,
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ifnull(pe.products_description_extra, 'N/A') as products_description_extra
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Time
Query String
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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 = '20110' and pd.language_id = 1
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<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: 0.5-2ug/mL<br>Immunohistochemistry: 5-20ug/mL<br>Immunocytochemistry: 5-20ug/mL<br>Optimal working dilutions must be determined by end user.
⇄⧉ncbi_pathways => string (527) "Adaptive Immune System Pathway||366160!!Amyloids Pathway||366238!!Antigen Pr...
$value['ncbi_pathways']
Adaptive Immune System Pathway||366160!!Amyloids Pathway||366238!!Antigen Presentation: Folding, Assembly And Peptide Loading Of Class I MHC Pathway||366163!!Antigen Processing And Presentation Pathway||83074!!Antigen Processing And Presentation Pathway||485!!Antigen Processing-Cross Presentation Pathway||477122!!Class I MHC Mediated Antigen Processing & Presentation Pathway||366161!!Cytokine Signaling In Immune System Pathway||366171!!Disease Pathway||530764!!Downstream Signaling In Naive CD8+ T Cells Pathway||138018
<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: 0.5-2ug/mL<br>Immunohistochemistry: 5-20ug/mL<br>Immunocytochemistry: 5-20ug/mL<br>Optimal working dilutions must be determined by end user.
⇄⧉ncbi_pathways => string (527) "Adaptive Immune System Pathway||366160!!Amyloids Pathway||366238!!Antigen Pr...
$value->a['ncbi_pathways']
Adaptive Immune System Pathway||366160!!Amyloids Pathway||366238!!Antigen Presentation: Folding, Assembly And Peptide Loading Of Class I MHC Pathway||366163!!Antigen Processing And Presentation Pathway||83074!!Antigen Processing And Presentation Pathway||485!!Antigen Processing-Cross Presentation Pathway||477122!!Class I MHC Mediated Antigen Processing & Presentation Pathway||366161!!Cytokine Signaling In Immune System Pathway||366171!!Disease Pathway||530764!!Downstream Signaling In Naive CD8+ T Cells Pathway||138018
<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: 0.5-2ug/mL<br>Immunohistochemistry: 5-20ug/mL<br>Immunocytochemistry: 5-20ug/mL<br>Optimal working dilutions must be determined by end user.
⇄⧉ncbi_pathways => string (527) "Adaptive Immune System Pathway||366160!!Amyloids Pathway||366238!!Antigen Pr...
$value->d['ncbi_pathways']
Adaptive Immune System Pathway||366160!!Amyloids Pathway||366238!!Antigen Presentation: Folding, Assembly And Peptide Loading Of Class I MHC Pathway||366163!!Antigen Processing And Presentation Pathway||83074!!Antigen Processing And Presentation Pathway||485!!Antigen Processing-Cross Presentation Pathway||477122!!Class I MHC Mediated Antigen Processing & Presentation Pathway||366161!!Cytokine Signaling In Immune System Pathway||366171!!Disease Pathway||530764!!Downstream Signaling In Naive CD8+ T Cells Pathway||138018
⇄⧉products_description => string (1236) "Principle of the Assay: The principle of the double antibody sandwich ELISA ...
$value[0]['_source']['products_description']
Principle of the Assay: The principle of the double antibody sandwich ELISA is represented in Figure 1. In this assay the NGAL present in samples reacts with the anti-NGAL antibodies which have been adsorbed to the surface of polystyrene microtitre wells. After the removal of unbound proteins by washing, the Detection Antibody, biotin conjugated anti-NGAL, is added and complexes are formed. Following a wash step, the horseradish peroxidase (HRP) conjugated Streptavidin is added and complexes are formed. After another washing step, the complexes are assayed by the addition of a chromogenic substrate, 3,3',5,5'-tetramethylbenzidine (TMB). The quantity of bound enzyme varies directly with the concentration of NGAL in the sample tested; thus, the absorbance, at 450 nm, is a measure of the concentration of NGAL in the test sample. The quantity of NGAL in the test sample can be interpolated from the standard curve constructed from the standards, and corrected for sample dilution.<br><br>Intended Uses: The NGAL test kit is a highly sensitive two-site enzyme linked immunoassay (ELISA) for measuring NGAL in rat biological samples. If the ELISA is to be used outside the intended use, the user may need to optimize for said use.
⇄⧉products_description => string (827) "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-Canine NGAL 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_description => string (676) "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 Bovine NGAL 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.
Antimicrobial Peptides Pathway||1457777!!Cytokine Signaling In Immune System Pathway||1269310!!Immune System Pathway||1269170!!Innate Immune System Pathway||1269203!!Interleukin-4 And 13 Signaling Pathway||1470923!!Iron Uptake And Transport Pathway||1269948!!Metal Sequestration By Antimicrobial Proteins Pathway||1457778!!Neutrophil Degranulation Pathway||1457780!!Signaling By Interleukins Pathway||1269318!!Transmembrane Transport Of Small Molecules Pathway||1269903
⇄⧉search_terms => string (582) "aaa22730 bovine no cross reaction with other factors typical testing data st...
$value[2]['_source']['search_terms']
aaa22730 bovine no cross reaction with other factors typical testing data standard curve for reference only aaa22730_sc elisa kit neutrophil gelatinase associated lipocalin ngal 2 lcn2 p25 24p3 msfi 22,457 da 25 kda alpha microglobulin related subunit of mmp 9 oncogene siderocalin hnl ngal_human 38455402 np_005555.2 p80188 nm_005564.4 p30150 q5syv9 q5syw0 q6fgl5 q92683 a6nii8 b4dwv4 b7zaa2 x83006 mrna samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 20 ng ml 0.312 sensitivity up to 0.06ng intra precision ngal2 da25 mmp9 range20
⇄⧉specificity => string (177) "This assay has high sensitivity and excellent specificity for detection of p...
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This assay has high sensitivity and excellent specificity for detection of pig NGAL. No significant cross-reactivity or interference between pig NGAL and analogues was observed.
⇄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 (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[3]['_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[3]['_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 (621) "Principle of the Assay: This assay employs the competitive inhibition enzyme...
$value[3]['_source']['products_description']
Principle of the Assay: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with NGAL. Standards or samples are added to the appropriate microtiter plate wells with Horseradish Peroxidase (HRP) conjugated antibody preparation specific for NGAL. The competitive inhibition reaction is launched between with pre-coated NGAL and NGAL in samples. A substrate solution is added to the wells and the color develops in opposite to the amount of NGAL in the samples. The color development is stopped and the intensity of the color is measured.
⇄⧉search_terms => string (714) "aaa15807 pig this assay has high sensitivity and excellent specificity for d...
$value[3]['_source']['search_terms']
aaa15807 pig this assay has high sensitivity and excellent specificity for detection of ngal no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa15807_td elisa kit neutrophil gelatinase associated lipocalin 2 lcn2 24p3 msfi p25 oncogene siderocalin migration stimulating factor inhibitor 25 kda alpha microglobulin related subunit mmp 9 22,457 da hnl ngal_human 38455402 np_005555.2 p80188 nm_005564.3 p30150 q5syv9 q5syw0 q6fgl5 q92683 a6nii8 b4dwv4 b7zaa2 600181 samples serum plasma tissue homogenates type quantitative competitive range 7.8 pg ml 500 < 1.95 intra precision within an cv lipocalin2 inhibitor25 mmp9 range7.8 ml500
⇄⧉products_description => string (826) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[4]['_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-Human NGAL 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_description => string (828) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[5]['_source']['products_description']
Principle of the Assay: As mentioned above, this kit utilizes the Double Antibody Sandwich ELISA technique. The pre-coated antibody is an anti-Porcine NGAL 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.
⇄⧉specificity => string (181) "This assay has high sensitivity and excellent specificity for detection of s...
$value[6]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of sheep NGAL. No significant cross-reactivity or interference between sheep NGAL 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 (621) "Principle of the Assay: This assay employs the competitive inhibition enzyme...
$value[6]['_source']['products_description']
Principle of the Assay: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with NGAL. Standards or samples are added to the appropriate microtiter plate wells with Horseradish Peroxidase (HRP) conjugated antibody preparation specific for NGAL. The competitive inhibition reaction is launched between with pre-coated NGAL and NGAL in samples. A substrate solution is added to the wells and the color develops in opposite to the amount of NGAL in the samples. The color development is stopped and the intensity of the color is measured.
⇄⧉search_terms => string (669) "aaa15601 sheep this assay has high sensitivity and excellent specificity for...
$value[6]['_source']['search_terms']
aaa15601 sheep this assay has high sensitivity and excellent specificity for detection of mouse igm no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa15601_td elisa kit neutrophil gelatinase associated lipocalin ngal 2 lcn2 24p3 msfi p25 oncogene siderocalin migration stimulating factor inhibitor 25 kda alpha microglobulin related subunit mmp 9 22,457 da hnl ngal_human 38455402 np_005555.2 p80188 nm_005564.3 p30150 q5syv9 q5syw0 q6fgl5 q92683 a6nii8 b4dwv4 b7zaa2 600181 samples serum plasma type competitive range 62.5 ng ml 4000 intra precision within an cv ngal2 inhibitor25 mmp9
⇄⧉specificity => string (376) "This assay has high sensitivity and excellent specificity for detection of N...
$value[7]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of NGAL. No significant cross-reactivity or interference between NGAL and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between NGAL and all the analogues, therefore, cross reaction may still exist in some cases.
⇄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 (35) "Store all reagents at 2-8 degree C."
⇄⧉products_description => string (1384) "Intended Uses: This NGAL ELISA kit is a 1.5 hour solid-phase ELISA designed ...
$value[7]['_source']['products_description']
Intended Uses: This NGAL ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Bovine NGAL. This ELISA kit for research use only, not for therapeutic or test applications!<br><br>Principle of the Assay: NGAL ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-NGAL antibody and an NGAL-HRP conjugate. The assay sample and buffer are incubated together with NGAL-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 NGAL concentration since NGAL from samples and NGAL-HRP conjugate compete for the anti-NGAL antibody binding site. Since the number of sites is limited, as more sites are occupied by NGAL from the sample, fewer sites are left to bind NGAL-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The NGAL concentration in each sample is interpolated from this standard curve.
⇄⧉search_terms => string (845) "aaa17035 bovine this assay has high sensitivity and excellent specificity fo...
$value[7]['_source']['search_terms']
aaa17035 bovine this assay has high sensitivity and excellent specificity for detection of ngal 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 aaa17035_sc elisa kit neutrophil gelatinase associated lipocalin 2 lcn2 24p3 msfi p25 oncogene siderocalin migration stimulating factor inhibitor 25 kda alpha microglobulin related subunit mmp 9 22,457 da hnl ngal_human 38455402 np_005555.2 p80188 nm_005564.3 p30150 q5syv9 q5syw0 q6fgl5 q92683 a6nii8 b4dwv4 b7zaa2 600181 cell biology samples serum plasma culture supernatants body fluid tissue homogenate type quantitative competitive 1.0 ng ml lipocalin2 inhibitor25 mmp9 competitive1.0
⇄⧉etc_term1 => string (216) "Samples||Guinea pig serum, plasma or cell culture supernatant and organizati...
$value[8]['_source']['etc_term1']
Samples||Guinea pig serum, plasma or cell culture supernatant and organizations in the natural and recombinant NGAL concentration.!!Assay Type||Sandwich!!Detection Range||2000 pg/ml-31.2 pg/ml!!Sensitivity||12 pg/ml.
⇄⧉products_description => string (680) "Principle of the Assay||This experiment use double-sandwich elisa technique ...
$value[8]['_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 Guinea pig NGAL 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.
⇄⧉products_description => string (824) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[9]['_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 NGAL 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.
⇄⧉specificity => string (376) "This assay has high sensitivity and excellent specificity for detection of N...
$value[10]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of NGAL. No significant cross-reactivity or interference between NGAL and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between NGAL and all the analogues, therefore, cross reaction may still exist in some cases.
⇄purity => string (3) "N/A"
$value[10]['_source']['purity']
⇄form => string (3) "N/A"
$value[10]['_source']['form']
⇄concentration => string (3) "N/A"
$value[10]['_source']['concentration']
⇄storage_stability => string (35) "Store all reagents at 2-8 degree C."
⇄⧉etc_term1 => string (157) "Samples||Serum, plasma, cell culture supernatants, body fluid and tissue hom...
$value[10]['_source']['etc_term1']
Samples||Serum, plasma, cell culture supernatants, body fluid and tissue homogenate!!Assay Type||Quantitative Competitive or Sandwich!!Sensitivity||1.0 ng/mL
⇄⧉products_description => string (1495) "Intended Uses: This NGAL ELISA kit is a 1.5 hour solid-phase ELISA designed ...
$value[10]['_source']['products_description']
Intended Uses: This NGAL ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Rat NGAL. This ELISA kit for research use only, not for therapeutic or test applications!<br><br>Principle of the Assay: NGAL ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for NGAL. Standards or samples are then added to the microtiter plate wells and NGAL if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of NGAL present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated polyclonal antibody, specific for NGAL are added to each well to "sandwich" the NGAL 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 NGAL 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 NGAL concentration in each sample is interpolated from this standard curve.
⇄⧉search_terms => string (848) "aaa16210 rat this assay has high sensitivity and excellent specificity for d...
$value[10]['_source']['search_terms']
aaa16210 rat this assay has high sensitivity and excellent specificity for detection of ngal 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 aaa16210_sc elisa kit neutrophil gelatinase associated lipocalin 2 lcn2 24p3 msfi p25 oncogene siderocalin migration stimulating factor inhibitor 25 kda alpha microglobulin related subunit mmp 9 22,457 da hnl ngal_human 38455402 np_005555.2 p80188 nm_005564.3 p30150 q5syv9 q5syw0 q6fgl5 q92683 a6nii8 b4dwv4 b7zaa2 600181 cell biology samples serum plasma culture supernatants body fluid tissue homogenate type quantitative competitive sandwich 1.0 ng ml lipocalin2 inhibitor25 mmp9 sandwich1.0
⇄⧉specificity => string (379) "This assay has high sensitivity and excellent specificity for detection of L...
$value[11]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of LCN-2. No significant cross-reactivity or interference between LCN-2 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between LCN-2 and all the analogues, therefore, cross reaction may still exist in some cases.
⇄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 (35) "Store all reagents at 2-8 degree C."
⇄⧉products_description => string (1404) "Principle of the Assay: LCN-2 ELISA kit applies the competitive enzyme immun...
$value[11]['_source']['products_description']
Principle of the Assay: LCN-2 ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-LCN-2 antibody and an LCN-2-HRP conjugate. The assay sample and buffer are incubated together with LCN-2-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 LCN-2 concentration since LCN-2 from samples and LCN-2-HRP conjugate compete for the anti-LCN-2 antibody binding site. Since the number of sites is limited, as more sites are occupied by LCN-2 from the sample, fewer sites are left to bind LCN-2-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The LCN-2 concentration in each sample is interpolated from this standard curve.<br><br>Intended Uses: This LCN-2 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Porcine LCN-2. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
⇄⧉search_terms => string (775) "aaa17197 porcine this assay has high sensitivity and excellent specificity f...
$value[11]['_source']['search_terms']
aaa17197 porcine this assay has high sensitivity and excellent specificity for detection of lcn2 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 aaa17197_sc elisa kit lipocalin 2 22,457 da neutrophil gelatinase associated 25 kda alpha microglobulin related subunit mmp 9 oncogene 24p3 siderocalin p25 hnl ngal ngal_human 21619839 aah33089.1 p30150 q5syv9 q5syw0 q6fgl5 q92683 a6nii8 b4dwv4 b7zaa2 600181 samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative competitive 1.0 ng ml lipocalin2 associated25 mmp9 competitive1.0
Assay Type||Quantitative Sandwich!!Samples||Serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids!!Detection Range||0.5-150ng/ml!!Sensitivity||0.24ng/ml
⇄⧉etc_term2 => string (403) "Intra-assay Precision||Intra-Assay Precision (Precision within an assay) Thr...
$value[12]['_source']['etc_term2']
Intra-assay Precision||Intra-Assay Precision (Precision within an assay) Three samples of known concentration were tested on one plate to assess intra-assay precision. Intra-Assay: CV<8%!!Inter-assay Precision||Inter-Assay Precision (Precision between assays) Three samples of known concentration were tested in separate assays to assess inter-assay precision. CV(%) = SD/mean x 100. Inter-Assay: CV<10%
⇄⧉products_description => string (901) "Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (EL...
$value[12]['_source']['products_description']
Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (ELISA). The plate has been pre-coated with Cat NGAL antibody. NGAL present in the sample is added and binds to antibodies coated on the wells. And then biotinylated Cat NGAL Antibody is added and binds to NGAL in the sample. Then Streptavidin-HRP is added and binds to the Biotinylated NGAL 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 Cat NGAL. 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 Cat Neutrophil Gelatinase-Associated Lipocalin (also known as NGAL) in serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids.
⇄⧉search_terms => string (701) "aaa19010 cat typical testing data standard curve for reference only aaa19010...
$value[12]['_source']['search_terms']
aaa19010 cat typical testing data standard curve for reference only aaa19010_sc elisa kit neutrophil gelatinase associated lipocalin ngal 2 lcn2 p25 24p3 msfi 22,457 da 25 kda alpha microglobulin related subunit of mmp 9 oncogene siderocalin hnl 38455402 np_005555.2 p80188 nm_005564.4 p30150 q5syv9 q5syw0 q6fgl5 q92683 a6nii8 b4dwv4 b7zaa2 samples serum plasma cell culture supernates ascites tissue homogenates or other biological fluids assay type quantitative sandwich detection range 0.5 150ng ml sensitivity 0.24ng intra precision within an three known concentration were tested on one plate to assess cv<8 inter between assays in separate cv = sd mean x 100 cv<10 ngal2 da25 mmp9 range0.5 x100
⇄⧉specificity => string (376) "This assay has high sensitivity and excellent specificity for detection of N...
$value[13]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of NGAL. No significant cross-reactivity or interference between NGAL and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between NGAL and all the analogues, therefore, cross reaction may still exist in some cases.
⇄purity => string (3) "N/A"
$value[13]['_source']['purity']
⇄form => string (3) "N/A"
$value[13]['_source']['form']
⇄concentration => string (3) "N/A"
$value[13]['_source']['concentration']
⇄storage_stability => string (35) "Store all reagents at 2-8 degree C."
⇄⧉products_description => string (1388) "Intended Uses: This NGAL ELISA kit is a 1.5 hour solid-phase ELISA designed ...
$value[13]['_source']['products_description']
Intended Uses: This NGAL ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Guinea pig NGAL. This ELISA kit for research use only, not for therapeutic or test applications!<br><br>Principle of the Assay: NGAL ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-NGAL antibody and an NGAL-HRP conjugate. The assay sample and buffer are incubated together with NGAL-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 NGAL concentration since NGAL from samples and NGAL-HRP conjugate compete for the anti-NGAL antibody binding site. Since the number of sites is limited, as more sites are occupied by NGAL from the sample, fewer sites are left to bind NGAL-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The NGAL concentration in each sample is interpolated from this standard curve.
⇄⧉search_terms => string (844) "aaa16301 guinea pig this assay has high sensitivity and excellent specificit...
$value[13]['_source']['search_terms']
aaa16301 guinea pig this assay has high sensitivity and excellent specificity for detection of ngal 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 aaa16301_sc elisa kit neutrophil gelatinase associated lipocalin lcn2 2 24p3 msfi p25 oncogene siderocalin migration stimulating factor inhibitor 25 kda alpha microglobulin related subunit mmp 9 22,457 da hnl ngal_human 38455402 np_005555.2 p80188 nm_005564.3 p30150 q5syv9 q5syw0 q6fgl5 q92683 a6nii8 b4dwv4 b7zaa2 600181 cell biology samples serum plasma culture supernatants body fluid tissue homogenate type quantitative competitive 0.1 ng ml lcn22 inhibitor25 mmp9 competitive0.1
⇄⧉products_description => string (828) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[14]['_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-Chicken LCN2 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.
25 kDa alpha-2-microglobulin-related subunit of MMP-91 PublicationManual assertion based on opinion iniRef.10"A 25 kDa alpha 2-microglobulin-related protein is a component of the 125 kDa form of human gelatinase."Triebel S., Blaeser J., Reinke H., Tschesche H.FEBS Lett. 314:386-388(1992) [PubMed] [Europe PMC] [Abstract]Cited for: PROTEIN SEQUENCE OF 51-61; 71-90; 132-136; 152-160 AND 178-192, SUBUNIT, INTERACTION WITH MMP9.
⇄sp_gene_name => string (4) "LCN2"
$value[14]['_source']['sp_gene_name']
⇄sp_gene_name_syn => string (70) "HNL; NGAL1 PublicationManual assertion based on opinion iniRef.1; NGAL"
⇄⧉testing_protocols => string (1173) "ICC (Immunocytochemistry)||ICC staining NGAL in SW480 cells (red). The nucle...
$value[15]['_source']['testing_protocols']
ICC (Immunocytochemistry)||ICC staining NGAL in SW480 cells (red). The nuclear counter stain is DAPI (blue).Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA29895_ICC6.jpg!!ICC (Immunocytochemistry)||ICC staining NGAL in NIH-3T3 cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA29895_ICC5.jpg!!ICC (Immunocytochemistry)||ICC staining NGAL in A431 cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA29895_ICC4.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded huamn liver tissue using anti-NGAL antibody. Counter stained with hematoxylin.||AAA29895_IHC3.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded human stomach cancer tissue using anti-NGAL antibody. Counter stained with hematoxylin.||AAA29895_IHC2.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded human spleen tissue using anti-NGAL Tubulin antibody. Counter stained with hematoxylin.||AAA29895_IHC.jpg
⇄⧉products_description => string (1094) "In addition to the monomeric mammalian progelatinase, two additional forms o...
$value[15]['_source']['products_description']
In addition to the monomeric mammalian progelatinase, two additional forms of progelatinase have been identified. The shorter of these additional forms is a covalently linked, disulfide-bridged protein that heterodimerizes with a short protein; an alpha2-Microglobulin-related protein known as neutrophil gelatinase-associated lipocalin (NGAL), which is moderately expressed in breast and lung tissues. NGAL belongs to the lipocalin family and has a high degree of similarity with rat alpha2-Microglobulin-related protein and mouse protein 24p3. NGAL is able to bind a derivative of the bacterial chemotactic peptide, suggesting that it has important immuno-modulatory functions. NGAL has been described as an inflammatory protein; it is released into the circulation as a result of the inflammatory activation of leukocytes initiated by the extra-corporeal circulation. In addition, NGAL synthesis is induced in epithelial cells in inflammatory and neoplastic colorectal diseases. In conclusion, NGAL may serve as a scavenger of bacterial products to function in the anti-inflammatory process.
ICC (Immunocytochemistry)||ICC staining Lipocalin-2 in SW480 cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA30316_ICC9.jpg!!ICC (Immunocytochemistry)||ICC staining Lipocalin-2 in Hela cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA30316_ICC8.jpg!!ICC (Immunocytochemistry)||ICC staining Lipocalin-2 in 293T cells (red). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.||AAA30316_ICC7.jpg!!IHC (Immunohistchemistry)||Immunohistochemical analysis of paraffin-embedded human pancreas tissue using anti-Lipocalin-2 antibody. Counter stained with hematoxylin.||AAA30316_IHC6.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded human uterus tissue using anti-Lipocalin-2 antibody. Counter stained with hematoxylin.||AAA30316_IHC5.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded human lung tissue using anti-Lipocalin-2 antibody. Counter stained with hematoxylin.||AAA30316_IHC4.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded human spleen tissue using anti-Lipocalin-2 antibody. Counter stained with hematoxylin.||AAA30316_IHC3.jpg!!IHC (Immunohistochemistry)||Immunohistochemical analysis of paraffin-embedded human stomach cancer tissue using anti-Lipocalin-2 antibody. Counter stained with hematoxylin.||AAA30316_IHC2.jpg!!WB (Western Blot)||Western blot analysis of Lipocalin-2 on A431 cells lysates using anti-Lipocalin-2 antibody at 1/500 dilution.||AAA30316_WB.jpg
⇄⧉products_description => string (1094) "In addition to the monomeric mammalian progelatinase, two additional forms o...
$value[16]['_source']['products_description']
In addition to the monomeric mammalian progelatinase, two additional forms of progelatinase have been identified. The shorter of these additional forms is a covalently linked, disulfide-bridged protein that heterodimerizes with a short protein; an alpha2-Microglobulin-related protein known as neutrophil gelatinase-associated lipocalin (NGAL), which is moderately expressed in breast and lung tissues. NGAL belongs to the lipocalin family and has a high degree of similarity with rat alpha2-Microglobulin-related protein and mouse protein 24p3. NGAL is able to bind a derivative of the bacterial chemotactic peptide, suggesting that it has important immuno-modulatory functions. NGAL has been described as an inflammatory protein; it is released into the circulation as a result of the inflammatory activation of leukocytes initiated by the extra-corporeal circulation. In addition, NGAL synthesis is induced in epithelial cells in inflammatory and neoplastic colorectal diseases. In conclusion, NGAL may serve as a scavenger of bacterial products to function in the anti-inflammatory process.
⇄⧉specificity => string (183) "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 DEFA3. No significant cross-reactivity or interference between human DEFA3 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_description => string (735) "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 DEFA3 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any DEFA3 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for DEFA3 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 DEFA3 bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄⧉ncbi_pathways => string (241) "Alpha-defensins Pathway||530758!!Defensins Pathway||530757!!Immune System Pa...
$value[17]['_source']['ncbi_pathways']
Alpha-defensins Pathway||530758!!Defensins Pathway||530757!!Immune System Pathway||106386!!Innate Immune System Pathway||106387!!Transcriptional Misregulation In Cancer Pathway||523016!!Transcriptional Misregulation In Cancer Pathway||522987
⇄⧉search_terms => string (555) "aaa15851 human this assay has high sensitivity and excellent specificity for...
$value[17]['_source']['search_terms']
aaa15851 human this assay has high sensitivity and excellent specificity for detection of defa3 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa15851_td elisa kit defensin alpha 3 neutrophil specific def3 hnp hnp3 hp peptide preproprotein hp3 10,245 da 2 hp2 def3_human 4885179 np_005208.1 p59666 nm_005217.3 p11479 q14125 604522 samples serum plasma tissue homogenates type quantitative sandwich range 1.87 ng ml 120 < 0.47 intra precision within an cv alpha3 da2 ml120
⇄specificity => string (73) "Specifically recognize NE, no obvious cross reaction with other analogues"
$value[18]['_source']['specificity']
⇄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 (156) "Store entire kit at 2-8C for short-term. For longer-term, please store the m...
$value[18]['_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[18]['_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.
NE (Neutrophil Elastase )/ELANE/PMN elastase/Medullasin/Bone marrow serine protease/Elastase-2
⇄products_gene_name => string (2) "NE"
$value[18]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[18]['_source']['products_gene_name_syn']
⇄⧉products_description => string (1589) "Background: Neutrophil Elastase (NE, ELANE), also known as HNE, is a chymotr...
$value[18]['_source']['products_description']
Background: Neutrophil Elastase (NE, ELANE), also known as HNE, is a chymotrypsin family serine protease that plays a key role in pathogen clearance. It is expressed by promyelocytes and stored in the intracellular azurophilic granules of polymorphonuclear leukocytes (PMN). These granules fuse with phagosomes, enabling Neutrophil Elastase to participate in the digestion and killing of endocytosed microbes. The enzyme is released by activated neutrophils at sites of inflammation, and it can remain associated with the cell surface or function as a component of neutrophil extracellular nets (NETs) which trap and kill microbial pathogens.<br><br>Principle of the Assay: This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Anti NE antibody was pre-coated onto the 96-well plate. The biotin conjugated anti NE 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 NE 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 NE in the sample was calculated by drawing a standard curve. The concentration of the target substance is proportional to the OD450 value.
⇄⧉search_terms => string (582) "aaa17638 mouse this assay has high sensitivity and excellent specificity for...
$value[18]['_source']['search_terms']
aaa17638 mouse this assay has high sensitivity and excellent specificity for detection of nagase no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa17638_sc elisa kit neutrophil elastase ne elane pmn medullasin bone marrow serine protease 2 preproprotein expressed ge hle hne ela2 scn1 e 28,518 da human leukocyte elne_human 4503549 np_001963.1 p08246 nm_001972.3 p09649 q6b0d9 q6ldp5 130130 samples serum plasma tissue homogenates other biological fluids type sandwich range 1.563 100ng ml protease2
Assay Type||Quantitative Sandwich!!Samples||Serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids!!Detection Range||0.1-40ng/mL!!Sensitivity||0.052ng/mL
⇄⧉etc_term2 => string (403) "Intra-assay Precision||Intra-Assay Precision (Precision within an assay) Thr...
$value[19]['_source']['etc_term2']
Intra-assay Precision||Intra-Assay Precision (Precision within an assay) Three samples of known concentration were tested on one plate to assess intra-assay precision. Intra-Assay: CV<8%!!Inter-assay Precision||Inter-Assay Precision (Precision between assays) Three samples of known concentration were tested in separate assays to assess inter-assay precision. CV(%) = SD/mean x 100. Inter-Assay: CV<10%
⇄products_name_oem => string (39) "Mouse neutrophil elastase, NE ELISA Kit"
$value[19]['_source']['products_name_oem']
⇄products_name_syn => string (3) "N/A"
$value[19]['_source']['products_name_syn']
⇄products_gene_name => string (2) "NE"
$value[19]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[19]['_source']['products_gene_name_syn']
⇄⧉products_description => string (872) "Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (EL...
$value[19]['_source']['products_description']
Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (ELISA). The plate has been pre-coated with Mouse NE antibody. NE present in the sample is added and binds to antibodies coated on the wells. And then biotinylated Mouse NE Antibody is added and binds to NE in the sample. Then Streptavidin-HRP is added and binds to the Biotinylated NE 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 NE. 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 Mouse neutrophil elastase (also known as NE) in serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids.
⇄products_references => string (3) "N/A"
$value[19]['_source']['products_references']
⇄⧉products_related_diseases => string (212) "Neutropenia||31!!Cyclic neutropenia||7!!NEUTROPENIA, SEVERE CONGENITAL, 1, A...
⇄⧉ncbi_pathways => string (499) "Activation Of Matrix Metalloproteinases Pathway||576264!!C-MYB Transcription...
$value[19]['_source']['ncbi_pathways']
Activation Of Matrix Metalloproteinases Pathway||576264!!C-MYB Transcription Factor Network Pathway||138073!!Degradation Of Collagen Pathway||730309!!Degradation Of The Extracellular Matrix Pathway||576263!!Extracellular Matrix Organization Pathway||576262!!Systemic Lupus Erythematosus Pathway||83122!!Systemic Lupus Erythematosus Pathway||534!!Transcriptional Misregulation In Cancer Pathway||523016!!Transcriptional Misregulation In Cancer Pathway||522987!!Amb2 Integrin Signaling Pathway||137945
Bone marrow serine protease; Elastase-2; Human leukocyte elastase; HLE; Medullasin; PMN elastase
⇄sp_gene_name => string (5) "ELANE"
$value[19]['_source']['sp_gene_name']
⇄sp_gene_name_syn => string (9) "ELA2; HLE"
$value[19]['_source']['sp_gene_name_syn']
⇄sp_entry_name => string (3) "N/A"
$value[19]['_source']['sp_entry_name']
⇄sp_mim => string (3) "N/A"
$value[19]['_source']['sp_mim']
⇄sp_interactions => string (6) "MPO||1"
$value[19]['_source']['sp_interactions']
⇄products_url => string (3) "N/A"
$value[19]['_source']['products_url']
⇄products_viewed => string (1) "0"
$value[19]['_source']['products_viewed']
⇄⧉search_terms => string (466) "aaa11105 mouse typical testing data standard curve for reference only aaa111...
$value[19]['_source']['search_terms']
aaa11105 mouse typical testing data standard curve for reference only aaa11105_sc elisa kit neutrophil elastase ne partial expressed elane ge hle hne ela2 scn1 pmn e 28,518 da bone marrow serine protease 2 human leukocyte medullasin 386981 aaa36359.1 p08246 p09649 q6b0d9 q6ldp5 samples serum plasma cell culture supernates lysates tissue homogenates assay type quantitative sandwich detection range 0.5ng ml 100ng sensitivity 0.22ng intra cv<8 inter cv<10 protease2
