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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Query
Database
2.11 ms
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ifnull(pdns.ncbi_summary, 'N/A') as ncbi_summary_pdns,
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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
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Database
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FROM `products_attributes`
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Database (4 total Queries, 4 of them unique across 2 Connections)
Time
Query String
2.03 ms
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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 = '23444' 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` = '23444'
Homology||Cow: 100%; Dog: 100%; Guinea Pig: 100%; Horse: 100%; Human: 100%; Mouse: 92%; Rabbit: 79%; Rat: 100%!!Immunogen||The immunogen is a synthetic peptide directed towards the N terminal region of human HOXB2
⇄⧉products_description => string (1051) "This is a rabbit polyclonal antibody against HOXB2. It was validated on West...
$value['products_description']
This is a rabbit polyclonal antibody against HOXB2. It was validated on Western Blot using a cell lysate as a positive control.<br><br>Target Description: HOXB2 is a member of the Antp homeobox family and encodes a nuclear protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox B genes located on chromosome 17. HOXB2 functions as a sequence-specific transcription factor that is involved in development. Increased expression of this gene is associated with pancreatic cancer.This gene is a member of the Antp homeobox family and encodes a nuclear protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox B genes located on chromosome 17. The encoded protein functions as a sequence-specific transcription factor that is involved in development. Increased expression of this gene is associated with pancreatic cancer. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Homology||Cow: 100%; Dog: 100%; Guinea Pig: 100%; Horse: 100%; Human: 100%; Mouse: 92%; Rabbit: 79%; Rat: 100%!!Immunogen||The immunogen is a synthetic peptide directed towards the N terminal region of human HOXB2
⇄⧉products_description => string (1051) "This is a rabbit polyclonal antibody against HOXB2. It was validated on West...
$value->a['products_description']
This is a rabbit polyclonal antibody against HOXB2. It was validated on Western Blot using a cell lysate as a positive control.<br><br>Target Description: HOXB2 is a member of the Antp homeobox family and encodes a nuclear protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox B genes located on chromosome 17. HOXB2 functions as a sequence-specific transcription factor that is involved in development. Increased expression of this gene is associated with pancreatic cancer.This gene is a member of the Antp homeobox family and encodes a nuclear protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox B genes located on chromosome 17. The encoded protein functions as a sequence-specific transcription factor that is involved in development. Increased expression of this gene is associated with pancreatic cancer. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Homology||Cow: 100%; Dog: 100%; Guinea Pig: 100%; Horse: 100%; Human: 100%; Mouse: 92%; Rabbit: 79%; Rat: 100%!!Immunogen||The immunogen is a synthetic peptide directed towards the N terminal region of human HOXB2
⇄⧉products_description => string (1051) "This is a rabbit polyclonal antibody against HOXB2. It was validated on West...
$value->d['products_description']
This is a rabbit polyclonal antibody against HOXB2. It was validated on Western Blot using a cell lysate as a positive control.<br><br>Target Description: HOXB2 is a member of the Antp homeobox family and encodes a nuclear protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox B genes located on chromosome 17. HOXB2 functions as a sequence-specific transcription factor that is involved in development. Increased expression of this gene is associated with pancreatic cancer.This gene is a member of the Antp homeobox family and encodes a nuclear protein with a homeobox DNA-binding domain. It is included in a cluster of homeobox B genes located on chromosome 17. The encoded protein functions as a sequence-specific transcription factor that is involved in development. Increased expression of this gene is associated with pancreatic cancer. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
⇄⧉etc_term1 => string (174) "Samples||Serum, plasma, Cell Culture Supernatants, body fluid and tissue hom...
$value[0]['_source']['etc_term1']
Samples||Serum, plasma, Cell Culture Supernatants, body fluid and tissue homogenate!!Assay Type||Competitive or Sandwich!!Detection Range||50-1000pg/mL!!Sensitivity||1.0pg/ml
⇄⧉etc_term2 => string (195) "Intended Uses||This TFPI ELISA kit is a 1.5 hour solid-phase ELISA designed ...
$value[0]['_source']['etc_term2']
Intended Uses||This TFPI ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Rat TFPI. This ELISA kit for research use only, not for therapeutic applications!
⇄⧉products_description => string (1177) "<b>Principle of the Assay: </b>TFPI ELISA kit applies the competitive enzyme...
$value[0]['_source']['products_description']
<b>Principle of the Assay: </b>TFPI ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-TFPI antibody and an TFPI-HRP conjugate. The assay sample and buffer are incubated together with TFPI-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 TFPI concentration since TFPI from samples and TFPI-HRP conjugate compete for the anti-TFPI antibody binding site. Since the number of sites is limited, as more sites are occupied by TFPI from the sample, fewer sites are left to bind TFPI-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The TFPI concentration in each sample is interpolated from this standard curve.
⇄⧉ncbi_pathways => string (365) "Complement And Coagulation Cascades Pathway||198880!!Complement And Coagulat...
$value[0]['_source']['ncbi_pathways']
Complement And Coagulation Cascades Pathway||198880!!Complement And Coagulation Cascades Pathway||83073!!Complement And Coagulation Cascades Pathway||484!!Extrinsic Pathway||106058!!Formation Of Fibrin Clot (Clotting Cascade) Pathway||106057!!Hemostasis Pathway||106028!!Integrated Breast Cancer Pathway||219801!!Syndecan-4-mediated Signaling Events Pathway||138064
⇄⧉search_terms => string (618) "aaa16521 rat typical testing data standard curve for reference only aaa16521...
$value[0]['_source']['search_terms']
aaa16521 rat typical testing data standard curve for reference only aaa16521_td elisa kit tissue factor pathway inhibitor tfpi isoform b lipoprotein associated coagulation epi tfi laci tfpi1 anti convertin extrinsic 28,653 da tfpi1_human 73760409 np_001027452.1 p10646 nm_001032281.2 o95103 q53ts4 152310 cardiovascular samples serum plasma cell culture supernatants body fluid and homogenate assay type competitive or sandwich detection range 50 1000pg ml sensitivity 1.0pg intended uses this is a 1.5 hour solid phase designed the quantitative determination of research use not therapeutic applications! range50 a1.5
⇄⧉products_description => string (826) "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-Mouse PEDF monoclonal antibody, while the detection antibody is a biotinylated polyclonal antibody. Samples and biotinylated antibodies are added into ELISA plate wells and washed out with PBS or TBS after their respective additions to the wells. Then Avidin-peroxidase conjugates are added to the wells in after. TMB substrate is used for coloration after the enzyme conjugate has already been thoroughly washed out of the wells by PBS or TBS. TMB reacts to form a blue product from the peroxidase activity, and finally turns to yellow after addition of the stop solution (Color Reagent C). The color intensity and quantity of target analyte in the sample are positively correlated.
⇄products_references => string (3) "N/A"
$value[1]['_source']['products_references']
⇄⧉products_related_diseases => string (113) "Nervous System Diseases||2!!Cell Transformation, Neoplastic||1!!Proteinuria|...
$value[1]['_source']['products_related_diseases']
Nervous System Diseases||2!!Cell Transformation, Neoplastic||1!!Proteinuria||1!!Lung Neoplasms||1!!Weight Loss||1
⇄⧉search_terms => string (619) "aaa12784 mouse no cross reaction with other factors typical testing data sta...
$value[1]['_source']['search_terms']
aaa12784 mouse no cross reaction with other factors typical testing data standard curve for reference only aaa12784_sc elisa kit pigment epithelium derived factor pedf serpin peptidase inhibitor clade f alpha 2 antiplasmin member 1 serpinf1 oi6 oi12 epc pig35 f1 cell proliferation inducing gene 35 protein serine or cysteine proteinase 46,312 da pedf_human 39725934 np_002606.3 p36955 nm_002615.5 q13236 q2tu83 q96ct1 q96r01 q9bwa4 f1t092 613982 samples serum plasma culture supernatant assay type quantitative sandwich detection range 50 ng ml 0.78 sensitivity up to 0.08 intra precision alpha2 member1 gene35 range50
⇄⧉specificity => string (181) "This assay has high sensitivity and excellent specificity for detection of h...
$value[2]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of human PEDF. No significant cross-reactivity or interference between human PEDF and analogues was observed.
⇄purity => string (3) "N/A"
$value[2]['_source']['purity']
⇄form => string (3) "N/A"
$value[2]['_source']['form']
⇄concentration => string (3) "N/A"
$value[2]['_source']['concentration']
⇄⧉storage_stability => string (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[2]['_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[2]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV%<8%. Three samples of known concentration were tested twenty times on one plate to assess.!!Inter-assay Precision||Inter-assay Precision (Precision between assays): CV%<10%. Three samples of known concentration were tested in twenty assays to assess.
⇄⧉products_description => string (731) "Principle of the Assay||This assay employs the quantitative sandwich enzyme ...
$value[2]['_source']['products_description']
Principle of the Assay||This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for PEDF has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any PEDF present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for PEDF 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 PEDF 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[2]['_source']['products_references']
⇄⧉products_related_diseases => string (166) "Nervous System Diseases||2!!Nerve Degeneration||1!!Urinary Bladder Neoplasms...
$value[2]['_source']['products_related_diseases']
Nervous System Diseases||2!!Nerve Degeneration||1!!Urinary Bladder Neoplasms||1!!Proteinuria||1!!Lung Neoplasms||1!!Cell Transformation, Neoplastic||1!!Weight Loss||1
⇄⧉search_terms => string (711) "aaa15386 human this assay has high sensitivity and excellent specificity for...
$value[2]['_source']['search_terms']
aaa15386 human this assay has high sensitivity and excellent specificity for detection of pedf no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa15386_td elisa kit pigment epithelium derived factor epc 1 pig35 proliferation inducing protein 35 serine cysteine proteinase inhibitor clade f alpha 2 antiplasmin serpin peptidase member serpinf1 oi6 oi12 f1 cell gene 46,312 da pedf_human 39725934 np_002606.3 p36955 nm_002615.5 q13236 q2tu83 q96ct1 q96r01 q9bwa4 f1t092 613982 samples serum urine culture supernates tissue homogenates type sandwich range 0.156 ng ml 10 0.039 intra precision within an cv epc1 protein35 alpha2 ml10
⇄⧉etc_term1 => string (212) "Samples||Human Serum, Plasma Or Cell Culture Supernatant And Organizations I...
$value[3]['_source']['etc_term1']
Samples||Human Serum, Plasma Or Cell Culture Supernatant And Organizations In The Natural And Recombinant Pdzd3 Concentration!!Assay Type||Sandwich!!Detection Range||20 ng/ml-0.312 ng/ml!!Sensitivity||0.06 ng/ml.
⇄⧉products_description => string (676) "Principle of the Assay: This experiment use double-sandwich elisa technique ...
$value[3]['_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 PDZD3 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_references => string (3) "N/A"
$value[3]['_source']['products_references']
⇄⧉products_related_diseases => string (113) "Nervous System Diseases||2!!Cell Transformation, Neoplastic||1!!Proteinuria|...
$value[3]['_source']['products_related_diseases']
Nervous System Diseases||2!!Cell Transformation, Neoplastic||1!!Proteinuria||1!!Lung Neoplasms||1!!Weight Loss||1
⇄⧉search_terms => string (666) "aaa12911 human no cross reaction with other factors typical testing data sta...
$value[3]['_source']['search_terms']
aaa12911 human no cross reaction with other factors typical testing data standard curve for reference only aaa12911_sc elisa kit pigment epithelium derived factor pedf serpin peptidase inhibitor clade f alpha 2 antiplasmin member 1 serpinf1 oi6 oi12 epc pig35 f1 cell proliferation inducing gene 35 protein serine or cysteine proteinase 46,312 da pedf_human 39725934 np_002606.3 p36955 nm_002615.5 q13236 q2tu83 q96ct1 q96r01 q9bwa4 f1t092 613982 samples serum plasma culture supernatant and organizations in the natural recombinant pdzd3 concentration assay type sandwich detection range 20 ng ml 0.312 sensitivity 0.06 intra precision alpha2 member1 gene35 range20
⇄⧉specificity => string (177) "This assay has high sensitivity and excellent specificity for detection of r...
$value[4]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of rat TFPI. No significant cross-reactivity or interference between rat TFPI and analogues was observed.
⇄purity => string (3) "N/A"
$value[4]['_source']['purity']
⇄form => string (3) "N/A"
$value[4]['_source']['form']
⇄concentration => string (3) "N/A"
$value[4]['_source']['concentration']
⇄⧉storage_stability => string (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[4]['_source']['storage_stability']
Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please refer to pdf manual for further storage instructions.
Samples||Serum, plasma, cell culture supernates, tissue homogenates!!Assay Type||Quantitative Sandwich!!Detection Range||7.8 ng/ml -500 ng/ml!!Sensitivity||Typically less than 1.95 ng/ml.
⇄⧉etc_term2 => string (326) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV...
$value[4]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV%<8%. Three samples of known concentration were tested twenty times on one plate to assess!!Inter-assay Precision||Inter-assay Precision (Precision between assays): CV%<10%. Three samples of known concentration were tested in twenty assays to assess.
⇄⧉products_description => string (731) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value[4]['_source']['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for TFPI has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any TFPI present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for TFPI 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 TFPI bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄⧉search_terms => string (739) "aaa15172 rat this assay has high sensitivity and excellent specificity for d...
$value[4]['_source']['search_terms']
aaa15172 rat this assay has high sensitivity and excellent specificity for detection of tfpi no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa15172_td elisa kit tissue factor pathway inhibitor lipoprotein associated coagulation epi laci tfi tfpi1 otthump00000163472 otthump00000205431 anti convertin extrinsic 34,436 da tfpi1_rabit 156119400 np_001095184.1 p19761 nm_001101714.1 q28828 samples serum plasma cell culture supernates homogenates type quantitative sandwich range 7.8 ng ml 500 typically less than 1.95 intra precision within an cv <8 three known concentration were tested twenty times on one plate to assess inter assays <10 in range7.8 ml500
⇄⧉products_description => string (1104) "Intended Uses: This immunoassay kit allows for the in vitro quantitative det...
$value[5]['_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.
⇄⧉search_terms => string (477) "aaa23351 mouse recombinant and natural human vegf b typical testing data sta...
$value[5]['_source']['search_terms']
aaa23351 mouse recombinant and natural human vegf b typical testing data standard curve for reference only aaa23351_sc elisa kit pigment epithelium derived factor pedf caspin serpin f1 stromal cell 3 sdf serpinf1 sdf3 46,234 da pedf_mouse 117606335 np_035470.3 nm_011340.3 p97298 o70629 o88691 samples serum plasma tissue homogenates culture supernates or other biological fluids detection range 15.6 1000 pg ml sensitivity <6.1 intra assay precision cv <=5.3 inter <=9.5 cell3
⇄⧉specificity => string (379) "This assay has high sensitivity and excellent specificity for detection of R...
$value[6]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of RPE65. No significant cross-reactivity or interference between RPE65 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between RPE65 and all the analogues, therefore, cross reaction may still exist in some cases.
⇄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 (35) "Store all reagents at 2-8 degree C."
⇄⧉products_description => string (1402) "Principle of the Assay: RPE65 ELISA kit applies the competitive enzyme immun...
$value[6]['_source']['products_description']
Principle of the Assay: RPE65 ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-RPE65 antibody and an RPE65-HRP conjugate. The assay sample and buffer are incubated together with RPE65-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 RPE65 concentration since RPE65 from samples and RPE65-HRP conjugate compete for the anti-RPE65 antibody binding site. Since the number of sites is limited, as more sites are occupied by RPE65 from the sample, fewer sites are left to bind RPE65-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The RPE65 concentration in each sample is interpolated from this standard curve.<br><br>Intended Uses: This RPE65 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Mouse RPE65. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
⇄⧉search_terms => string (717) "aaa27142 mouse this assay has high sensitivity and excellent specificity for...
$value[6]['_source']['search_terms']
aaa27142 mouse this assay has high sensitivity and excellent specificity for detection of rpe65 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 aaa27142_sc elisa kit retinoid isomerohydrolase retinal pigment epithelium specific protein 65kda retinol isomerase trans retinyl palmitate hydrolase 65 kda 60,930 da rpe65_chick 45385809 np_990215.1 q9ygx2 nm_204884.1 samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative competitive 0.1 ng ml hydrolase65 competitive0.1
⇄⧉specificity => string (379) "This assay has high sensitivity and excellent specificity for detection of R...
$value[7]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of RPE65. No significant cross-reactivity or interference between RPE65 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between RPE65 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 (1402) "Principle of the Assay: RPE65 ELISA kit applies the competitive enzyme immun...
$value[7]['_source']['products_description']
Principle of the Assay: RPE65 ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-RPE65 antibody and an RPE65-HRP conjugate. The assay sample and buffer are incubated together with RPE65-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 RPE65 concentration since RPE65 from samples and RPE65-HRP conjugate compete for the anti-RPE65 antibody binding site. Since the number of sites is limited, as more sites are occupied by RPE65 from the sample, fewer sites are left to bind RPE65-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The RPE65 concentration in each sample is interpolated from this standard curve.<br><br>Intended Uses: This RPE65 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human RPE65. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
⇄⧉search_terms => string (717) "aaa27343 human this assay has high sensitivity and excellent specificity for...
$value[7]['_source']['search_terms']
aaa27343 human this assay has high sensitivity and excellent specificity for detection of rpe65 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 aaa27343_sc elisa kit retinoid isomerohydrolase retinal pigment epithelium specific protein 65kda retinol isomerase trans retinyl palmitate hydrolase 65 kda 60,930 da rpe65_chick 45385809 np_990215.1 q9ygx2 nm_204884.1 samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative competitive 0.1 ng ml hydrolase65 competitive0.1
⇄⧉specificity => string (382) "This assay has high sensitivity and excellent specificity for detection of A...
$value[8]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of ATPIF1. No significant cross-reactivity or interference between ATPIF1 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between ATPIF1 and all the analogues, therefore, cross reaction may still exist in some cases.
⇄purity => string (3) "N/A"
$value[8]['_source']['purity']
⇄form => string (3) "N/A"
$value[8]['_source']['form']
⇄concentration => string (3) "N/A"
$value[8]['_source']['concentration']
⇄storage_stability => string (35) "Store all reagents at 2-8 degree C."
⇄⧉products_description => string (1415) "Principle of the Assay: ATPIF1 ELISA kit applies the competitive enzyme immu...
$value[8]['_source']['products_description']
Principle of the Assay: ATPIF1 ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-ATPIF1 antibody and an ATPIF1-HRP conjugate. The assay sample and buffer are incubated together with ATPIF1-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 ATPIF1 concentration since ATPIF1 from samples and ATPIF1-HRP conjugate compete for the anti-ATPIF1 antibody binding site. Since the number of sites is limited, as more sites are occupied by ATPIF1 from the sample, fewer sites are left to bind ATPIF1-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The ATPIF1 concentration in each sample is interpolated from this standard curve.<br><br>Intended Uses: This ATPIF1 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human ATPIF1. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
⇄⧉search_terms => string (722) "aaa27310 human this assay has high sensitivity and excellent specificity for...
$value[8]['_source']['search_terms']
aaa27310 human this assay has high sensitivity and excellent specificity for detection of atpif1 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 aaa27310_sc elisa kit atpase inhibitor mitochondrial isoform 3 inhibitory factor 1 ip atpi atpip if1 protein f o atp synthase 6,592 da if atif1_human 30260192 np_835498.1 q9uii2 nm_178191.2 q5jxl8 q6iaq7 q9bsl9 614981 samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative competitive 0.1 ng ml isoform3 factor1 competitive0.1
⇄⧉specificity => string (379) "This assay has high sensitivity and excellent specificity for detection of A...
$value[9]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of ATPIF. No significant cross-reactivity or interference between ATPIF and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between ATPIF and all the analogues, therefore, cross reaction may still exist in some cases.
⇄purity => string (3) "N/A"
$value[9]['_source']['purity']
⇄form => string (3) "N/A"
$value[9]['_source']['form']
⇄concentration => string (3) "N/A"
$value[9]['_source']['concentration']
⇄storage_stability => string (35) "Store all reagents at 2-8 degree C."
⇄⧉products_description => string (1402) "Principle of the Assay: ATPIF ELISA kit applies the competitive enzyme immun...
$value[9]['_source']['products_description']
Principle of the Assay: ATPIF ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-ATPIF antibody and an ATPIF-HRP conjugate. The assay sample and buffer are incubated together with ATPIF-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 ATPIF concentration since ATPIF from samples and ATPIF-HRP conjugate compete for the anti-ATPIF antibody binding site. Since the number of sites is limited, as more sites are occupied by ATPIF from the sample, fewer sites are left to bind ATPIF-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The ATPIF concentration in each sample is interpolated from this standard curve.<br><br>Intended Uses: This ATPIF ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Mouse ATPIF. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
⇄⧉search_terms => string (722) "aaa27290 mouse this assay has high sensitivity and excellent specificity for...
$value[9]['_source']['search_terms']
aaa27290 mouse this assay has high sensitivity and excellent specificity for detection of atpif1 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 aaa27290_sc elisa kit atpase inhibitor mitochondrial isoform 3 inhibitory factor 1 ip atpi atpip if1 protein f o atp synthase 6,592 da if atif1_human 30260192 np_835498.1 q9uii2 nm_178191.2 q5jxl8 q6iaq7 q9bsl9 614981 samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative competitive 1.0 pg ml isoform3 factor1 competitive1.0
⇄⧉specificity => string (193) "This assay has high sensitivity and excellent specificity for detection of h...
$value[10]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of human alpha2 -AP. No significant cross-reactivity or interference between human alpha2 -AP and analogues was observed.
⇄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 (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[10]['_source']['storage_stability']
Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please refer to pdf manual for further storage instructions.
Samples||Serum, plasma!!Assay Type||Sandwich!!Detection Range||15.6 pg/ml -1000 pg/ml.!!Sensitivity||The minimum detectable dose of human alpha2 -AP is typically less than 3.9 pg/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.
⇄⧉etc_term2 => string (327) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): CV...
$value[10]['_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 alpha2-Antiplasmin; alpha2-AP ELISA Kit; A2AP; AAP; ALPHA-2-PI; API; PLI; OTTHUMP00000115656; alpha-2-antiplasmin; alpha-2-plasmin inhibitor; serine (or cysteine) proteinase inhibitor; clade F (alpha-2 antiplasmin; pigment epithelium derived; serpin peptidase inhibitor; clade F (alpha-2 antiplasmin; pigment epithelium derived factor); member 2
⇄products_gene_name => string (8) "SERPINF2"
$value[10]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[10]['_source']['products_gene_name_syn']
⇄⧉products_description => string (758) "<b>Principle of the assay: </b>This assay employs the quantitative sandwich ...
$value[10]['_source']['products_description']
<b>Principle of the assay: </b>This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for alpha2-AP has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any alpha2-AP present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for alpha2-AP 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 alpha2-AP bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄⧉search_terms => string (867) "aaa15039 human this assay has high sensitivity and excellent specificity for...
$value[10]['_source']['search_terms']
aaa15039 human this assay has high sensitivity and excellent specificity for detection of alpha2 ap no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa15039_td elisa kit serpin peptidase inhibitor clade f alpha 2 antiplasmin pigment epithelium derived factor member a2ap aap pi api pli otthump00000115656 plasmin serine cysteine proteinase serpinf2 isoform a f2 54,566 da a2ap_human 115583663 np_000925.2 p08697 nm_000934.3 q8n5u7 q9ucg2 q9ucg3 b4e1b7 613168 samples serum plasma type sandwich range 15.6 pg ml 1000 the minimum detectable dose is typically less than 3.9 lower limit lld defined as lowest protein concentration that could be differentiated from zero it determined mean o.d value 20 replicates added by their three deviations intra precision within an cv than3.9 value20
<b>Storage:</b><br>Avoid repeated freeze/thaw cycles.<br>Store at 2-8 degree C for one month. <br>Aliquot and store at -80 degree C for 12 months.<br><br><b>Stability Test:</b><br>The 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.
⇄app_tested => string (57) "Positive Control; Immunogen; SDS-PAGE; Western Blot (WB)."
$value[11]['_source']['app_tested']
⇄app_notes => string (75) "(May be suitable for use in other assays to be determined by the end user.)"
Traits||Freeze-dried powder!!Predicted isoelectric point||6.9!!Phenomenon Explanation||The possible reasons that the actual band size differs from the predicted are as follows:<br>1. Splice variants: Alternative splicing may create different sized proteins from the same gene.<br>2. Relative charge: The composition of amino acids may affects the charge of the protein.<br>3. Post-translational modification: Phosphorylation, glycosylation, methylation etc.<br>4. Post-translation cleavage: Many proteins are synthesized as pro-proteins, and then cleaved to give the active form.<br>5. Polymerization of the target protein: Dimerization, multimerization etc.!!Usage||Reconstitute in 10mM PBS (pH7.4) to a concentration of 0.1-1.0 mg/mL. Do not vortex.
⇄⧉search_terms => string (1303) "aaa21172 293f cell homo sapiens human > 95 pbs ph7.4 containing 0.01 tween80...
$value[11]['_source']['search_terms']
aaa21172 293f cell homo sapiens human > 95 pbs ph7.4 containing 0.01 tween80 5 trehalose positive control immunogen sds page western blot wb may be suitable for use in other assays to determined by the end user aaa21172_sds protein plasmin antiplasmin complex pap eukaryotic alpha 2 isoform a serpin peptidase inhibitor clade f pigment epithelium derived factor member serpinf2 aap api pli a2ap pi f2 ap serine or cysteine proteinase predicted molecular mass 109.4kda accurate 120kda as reducing conditions a2ap_human 115583663 np_000925.2 p08697 nm_000934.3 p00747 262850 signal transduction enzyme kinase hematology proteins ep source expression tags n terminal his tag subcellular location secreted traits freeze dried powder isoelectric point 6.9 phenomenon explanation possible reasons that actual band size differs from are follows 1 splice variants alternative splicing create different sized same gene relative charge composition of amino acids affects 3 post translational modification phosphorylation glycosylation methylation etc 4 translation cleavage many synthesized pro and then cleavedto give active form polymerization target dimerization multimerization usage reconstitute ddh2o concentration 0 0.5 mg ml do not vortex >95 tween805 alpha2 point6.9 follows1 affects3 etc4 concentration0
⇄⧉products_description => string (824) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[12]['_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 PLGF 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 (404) "aaa13032 rat typical testing data standard curve for reference only aaa13032...
$value[12]['_source']['search_terms']
aaa13032 rat typical testing data standard curve for reference only aaa13032_sc elisa kit placenta growth factor plgf isoform 1 placental pgf pigf ai854365 17,876 da plgf_mouse 6679289 np_032853.1 p49764 nm_008827.3 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 1000 pg ml 15.6 sensitivity up to 5 intra precision <= 8 inter 12 isoform1 to5 <=8 inter12
⇄⧉specificity => string (171) "This assay has high sensitivity and excellent specificity for detection of I...
$value[13]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of ITIH5. No significant cross-reactivity or interference between ITIH5 and analogues was observed.
⇄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 (475) "The stability of kit is determined by the loss rate of activity. The loss ra...
$value[13]['_source']['storage_stability']
The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. <br>To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.
Assay Type||Double-antibody Sandwich!!Samples||Serum, Plasma, Tissue homogenates, Cell lysates, Cell culture supernates and other biological fluids!!Detection Range||3.12-200ng/mL!!Sensitivity||1.37ng/mL
⇄⧉etc_term2 => string (416) "Intra-assay Precision||Intra-assay Precision (Precision within an assay): 3 ...
$value[13]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level ITIH5 were tested 20 times on one plate, respectively. Intra-Assay: CV<10%!!Inter-assay Precision||Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level ITIH5 were tested on 3 different plates, 8 replicates in each plate. CV(%) = SD/meanX100. Inter-Assay: CV<12%
⇄products_name_syn => string (44) "Inter-alpha-trypsin inhibitor heavy chain H5"
$value[13]['_source']['products_name_syn']
⇄products_gene_name => string (5) "ITIH5"
$value[13]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[13]['_source']['products_gene_name_syn']
⇄⧉products_description => string (934) "Intended Uses: The kit is a sandwich enzyme immunoassay for in vitro quantit...
$value[13]['_source']['products_description']
Intended Uses: The kit is a sandwich enzyme immunoassay for in vitro quantitative measurement of ITIH5 in human plasma.<br><br>Principle of the Assay: The microplate provided in this kit has been pre-coated with an antibody specific to ITIH5. Standards or samples are then added to the appropriate microplate wells with a biotin-conjugated antibody specific to ITIH5. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain ITIH5, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm +/- 10nm. The concentration of ITIH5 in the samples is then determined by comparing the O.D. of the samples to the standard curve.
⇄⧉search_terms => string (704) "aaa20710 human this assay has high sensitivity and excellent specificity for...
$value[13]['_source']['search_terms']
aaa20710 human this assay has high sensitivity and excellent specificity for detection of itih5 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa20710_sc elisa kit inter alpha globulin inhibitor h5 trypsin heavy chain isoform 2 family member 5 iti hc5 pp14776 27,191 da kiaa1953 itih5_human 312434033 np_116206.4 q86ux2 nm_032817.5 q5t664 q5t665 q5t666 q6ai60 q6uxb7 q8tf48 q8wyv2 q96k70 609783 metabolic pathway samples plasma type quantitative sandwich range 7.8 500ng ml < 3.7ng intra precision within an 3 with low middle level were tested 20 times on one plate respectively cv isoform2 member5 range7.8 an3 tested20
Assay Type||Quantitative Sandwich!!Samples||Serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids!!Detection Range||8-1800ng/L!!Sensitivity||4.02ng/L
⇄⧉etc_term2 => string (403) "Intra-assay Precision||Intra-Assay Precision (Precision within an assay) Thr...
$value[14]['_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 (889) "Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (EL...
$value[14]['_source']['products_description']
Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (ELISA). The plate has been pre-coated with Human PLGF antibody. PLGF present in the sample is added and binds to antibodies coated on the wells. And then biotinylated Human PLGF Antibody is added and binds to PLGF in the sample. Then Streptavidin-HRP is added and binds to the Biotinylated PLGF 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 PLGF. 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 placenta growth factor (also known as PLGF) in serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids.
⇄⧉search_terms => string (391) "aaa11300 human typical testing data standard curve for reference only aaa113...
$value[14]['_source']['search_terms']
aaa11300 human typical testing data standard curve for reference only aaa11300_sc elisa kit placenta growth factor plgf isoform 1 placental pgf pigf ai854365 17,876 da 6679289 np_032853.1 p49764 nm_008827.3 samples serum plasma cell culture supernates lysates tissue homogenates assay type quantitative sandwich detection range 8ng l 1800ng sensitivity 4.02ng intra cv<8 inter cv<10 isoform1
⇄⧉storage_stability => string (350) "Store at 4 degree C or at -20 degree C if preferred. Storage in frost-free f...
$value[15]['_source']['storage_stability']
Store at 4 degree C or at -20 degree C if preferred. Storage in frost-free freezers is not recommended. This product should be stored undiluted. Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use.<br>Shelf Life: 18 months from date of despatch.
⇄products_name_oem => string (38) "SHEEP ANTI HUMAN ALPHA 2 MACROGLOBULIN"
$value[15]['_source']['products_name_oem']
⇄products_name_syn => string (3) "N/A"
$value[15]['_source']['products_name_syn']
⇄products_gene_name => string (3) "N/A"
$value[15]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[15]['_source']['products_gene_name_syn']
⇄⧉products_description => string (295) "Sheep anti Human alpha 2 macroglobulin antibody recognizes human alpha-2-mac...
$value[15]['_source']['products_description']
Sheep anti Human alpha 2 macroglobulin antibody recognizes human alpha-2-macroglobulin, a secreted protease inhibitor known to suppress the function of all four classes of proteinases. Sheep anti Human alpha 2 macroglobulin antibody exhibits minimal cross reactivity with related serum proteins.
⇄products_references => string (3) "N/A"
$value[15]['_source']['products_references']
⇄⧉products_related_diseases => string (199) "Nervous System Diseases||96!!Mental Disorders||84!!Alzheimer Disease||82!!In...
⇄⧉ncbi_protein_info => string (99) "alpha-2-macroglobulin; C3 and PZP-like alpha-2-macroglobulin domain-containi...
$value[15]['_source']['ncbi_protein_info']
alpha-2-macroglobulin; C3 and PZP-like alpha-2-macroglobulin domain-containing protein 5; alpha-2-M
⇄ncbi_chrom_loc => string (3) "N/A"
$value[15]['_source']['ncbi_chrom_loc']
⇄ncbi_gene_id => string (1) "2"
$value[15]['_source']['ncbi_gene_id']
⇄ncbi_mol_weight => string (10) "163,291 Da"
$value[15]['_source']['ncbi_mol_weight']
⇄⧉ncbi_pathways => string (470) "Complement And Coagulation Cascades Pathway||198880!!Complement And Coagulat...
$value[15]['_source']['ncbi_pathways']
Complement And Coagulation Cascades Pathway||198880!!Complement And Coagulation Cascades Pathway||83073!!Complement And Coagulation Cascades Pathway||484!!Degradation Of The Extracellular Matrix Pathway||576263!!Extracellular Matrix Organization Pathway||576262!!Formation Of Fibrin Clot (Clotting Cascade) Pathway||106057!!HDL-mediated Lipid Transport Pathway||106158!!Hemostasis Pathway||106028!!IL6-mediated Signaling Events Pathway||137932!!Intrinsic Pathway||106059
⇄⧉products_description => string (822) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[16]['_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 TF 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 (424) "aaa12953 rat no cross reaction with other factors typical testing data stand...
$value[16]['_source']['search_terms']
aaa12953 rat no cross reaction with other factors typical testing data standard curve for reference only aaa12953_sc elisa kit tissue factor tf coagulation iii thromboplastin f3 tfa cd142 27,145 da cd_antigen tf_human 339508 aaa36734.1 p13726 q6fhg2 q86wh4 d3dt47 134390 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 1000 pg ml 15.6 sensitivity up to 5 intra precision to5
⇄⧉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 HIF-1. No significant cross-reactivity or interference between Human HIF-1 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 (22) "Store at 2-8 degree C."
Assay Type||Quantitative Sandwich!!Samples||Serum, plasma, tissue homogenates and other biological fluids!!Detection Range||62.5 pg/mL - 4000 pg/mL!!Sensitivity||31.25 pg/mL (mean of 6 independent assays)
⇄⧉etc_term2 => string (420) "Intra-assay Precision||Intra-assay Precision (Precision within an assay) Thr...
$value[17]['_source']['etc_term2']
Intra-assay Precision||Intra-assay Precision (Precision within an assay) Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision. Intra-Assay: CV<8%!!Inter-assay Precision||Inter-assay Precision (Precision between assays) Three samples of known concentration were tested in forty separate assays to assess inter-assay precision. CV(%) = SD/meanX100. Inter-Assay: CV<12%
⇄⧉products_description => string (955) "Principle of the Assay: This assay employs a two-site sandwich ELISA to quan...
$value[17]['_source']['products_description']
Principle of the Assay: This assay employs a two-site sandwich ELISA to quantitate HIF-1 in Human serum, plasma, tissue homogenates. An antibody specific for HIF-1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any HIF-1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for HIF-1 is added to the wells. After washing, Streptavidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of HIF-1 bound in the initial step. The color development is stopped and the intensity of the color is measured.<br><br>Intended Uses: For the quantitative detection of Human Hypoxia-inducible factor 1 (HIF-1) concentration in serum, plasma, tissue homogenates and other biological fluids.
⇄products_references => string (3) "N/A"
$value[17]['_source']['products_references']
⇄⧉products_related_diseases => string (203) "Neoplasms||2895!!Carcinoma||1205!!Nervous System Diseases||584!!Inflammation...
⇄⧉search_terms => string (647) "aaa13232 human this assay has high sensitivity and excellent specificity for...
$value[17]['_source']['search_terms']
aaa13232 human this assay has high sensitivity and excellent specificity for detection of hif 1 no significant cross reactivity or interference between analogues was observed elisa kit hypoxia inducible factor alpha isoform 3 subunit hif1a hif1 mop1 pasd8 1a bhlhe78 1alpha 95,634 da arnt interacting protein basic helix loop pas 340545531 np_001230013.1 q16665 nm_001243084.1 q53xp6 q96pt9 q9upb1 c0lzj3 u22431 mrna samples serum plasma tissue homogenates other biological fluids type quantitative sandwich range 62.5 pg ml 4000 31.25 intra precision within an three known concentration were tested twenty times on one plate to assess cv isoform3
⇄⧉products_description => string (827) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[18]['_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 IL-33 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.
interleukin-33; IL-33; IL-1F11; DVS27-related protein; interleukin-1 family member 11; nuclear factor for high endothelial venules; nuclear factor from high endothelial venules
⇄⧉search_terms => string (562) "aaa12426 human typical testing data standard curve for reference only aaa124...
$value[18]['_source']['search_terms']
aaa12426 human typical testing data standard curve for reference only aaa12426_sc elisa kit interleukin 33 il isoform 3 il33 dvs27 il1f11 nf hev nfehev c9orf26 1f11 related protein 1 family member 11 nuclear factor high endothelial venules from 16,250 da nfhev il33_human 314122337 np_001186570.1 o95760 nm_001199641.1 q2yej5 b2r8l1 b4dj35 b4e1q9 d3dri5 e7eax4 608678 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 1000 pg ml 15.6 sensitivity up to 5 intra precision interleukin33 isoform3 protein1 member11 to5
⇄⧉products_description => string (829) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[19]['_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 IL-33 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.
interleukin-33; IL-33; IL-1F11; DVS27-related protein; interleukin-1 family member 11; nuclear factor for high endothelial venules; nuclear factor from high endothelial venules
⇄⧉search_terms => string (564) "aaa12884 porcine typical testing data standard curve for reference only aaa1...
$value[19]['_source']['search_terms']
aaa12884 porcine typical testing data standard curve for reference only aaa12884_sc elisa kit interleukin 33 il isoform 3 il33 dvs27 il1f11 nf hev nfehev c9orf26 1f11 related protein 1 family member 11 nuclear factor high endothelial venules from 16,250 da nfhev il33_human 314122337 np_001186570.1 o95760 nm_001199641.1 q2yej5 b2r8l1 b4dj35 b4e1q9 d3dri5 e7eax4 608678 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 1000 pg ml 15.6 sensitivity up to 5 intra precision interleukin33 isoform3 protein1 member11 to5
