Highly validated and characterized monoclonal/polyclonal
antibodies and recombinant
proteins
The majority of AAA Biotech’s antibodies are highly validated and can be use in multiple
applications such as ELISA, FC,
ICC, IF, IHC, IP, WB, etc. We have antibodies available for rare species, in multiple conjugated
forms or recombinant
antibodies.
As for our high quality proteins, the majority have 90% purity, detected by SDS-PAGE while some are
available in
different tags such as Flag, GST, His, MBP, etc. We also carry high quality native and biologically
active proteins.
AAA Biotech is constantly working to expand our capacity to provide recombinant proteins and
antibodies to most
target proteins.
SELECT `p`.*, `pd`.*, IFNULL(pdns.ncbi_summary, "N/A") as ncbi_summary_pdns, IFNULL(pdns.sp_comments, "N/A") as sp_comments_pdns, IFNULL(pdns.ncbi_research_articles, "N/A") as ncbi_research_articles_pdns, IFNULL(pe.products_description_extra, "N/A") as products_description_extra
FROM (`products`, `products` as `p`)
LEFT OUTER JOIN `products_description` as `pd` ON `p`.`products_id` = `pd`.`products_id`
LEFT OUTER JOIN `products_description_ncbi_sp` as `pdns` ON `p`.`products_id` = `pdns`.`products_id`
LEFT OUTER JOIN `products_extra` as `pe` ON `p`.`products_id` = `pe`.`products_id`
WHERE `p`.`products_id` = '18587'
AND `pd`.`language_id` = 1
LIMIT 1
Query
Database
5.96 ms
select p.*, pd.*,
ifnull(pdns.ncbi_summary, 'N/A') as ncbi_summary_pdns,
ifnull(pdns.sp_comments, 'N/A') as sp_comments_pdns,
ifnull(pdns.ncbi_research_articles, 'N/A') as ncbi_research_articles_pdns,
ifnull(pe.products_description_extra, 'N/A') as products_description_extra
from products p
LEFT OUTER JOIN products_description pd on p.products_id = pd.products_id
LEFT OUTER JOIN products_description_ncbi_sp pdns on p.products_id = pdns.products_id
LEFT OUTER JOIN products_extra pe on p.products_id = pe.products_id
where p.products_id = '18587' and pd.language_id = 1
Query
Database
1.98 ms
SELECT `options_values_price` as `price`, `products_options_values_name` as `package`
FROM `products_attributes`
JOIN `products_options_values` ON `products_options_values`.`products_options_values_id` = `products_attributes`.`options_values_id`
WHERE `products_attributes`.`products_id` = '18587'
Database (4 total Queries, 4 of them unique across 2 Connections)
Time
Query String
2.29 ms
SELECT `p`.*, `pd`.*, IFNULL(pdns.ncbi_summary, "N/A") as ncbi_summary_pdns, IFNULL(pdns.sp_comments, "N/A") as sp_comments_pdns, IFNULL(pdns.ncbi_research_articles, "N/A") as ncbi_research_articles_pdns, IFNULL(pe.products_description_extra, "N/A") as products_description_extra
FROM (`products`, `products` as `p`)
LEFT OUTER JOIN `products_description` as `pd` ON `p`.`products_id` = `pd`.`products_id`
LEFT OUTER JOIN `products_description_ncbi_sp` as `pdns` ON `p`.`products_id` = `pdns`.`products_id`
LEFT OUTER JOIN `products_extra` as `pe` ON `p`.`products_id` = `pe`.`products_id`
WHERE `p`.`products_id` = '18587'
AND `pd`.`language_id` = 1
LIMIT 1
select p.*, pd.*,
ifnull(pdns.ncbi_summary, 'N/A') as ncbi_summary_pdns,
ifnull(pdns.sp_comments, 'N/A') as sp_comments_pdns,
ifnull(pdns.ncbi_research_articles, 'N/A') as ncbi_research_articles_pdns,
ifnull(pe.products_description_extra, 'N/A') as products_description_extra
from products p
LEFT OUTER JOIN products_description pd on p.products_id = pd.products_id
LEFT OUTER JOIN products_description_ncbi_sp pdns on p.products_id = pdns.products_id
LEFT OUTER JOIN products_extra pe on p.products_id = pe.products_id
where p.products_id = '18587' 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` = '18587'
⇄⧉products_description => string (136) "Increases the permeability of the small intestine mucosa by affecting the st...
$value['products_description']
Increases the permeability of the small intestine mucosa by affecting the structure of intercellular tight junctions (zonula occludens).
⇄⧉products_references => string (1218) "Cloning of a gene (zot) encoding a new toxin produced by Vibrio cholerae.Bau...
$value['products_references']
Cloning of a gene (zot)
encoding a new toxin produced by Vibrio cholerae.Baudry B., Fasano A., Ketley J., Kaper J.B.Infect. Immun. 60:428-434(1992)
Cloning and nucleotide sequence analysis of the virulence gene cassette from Vibrio cholerae KNIH002 isolated in Korea.Shin H.J., Park Y.C., Kim Y.C.Misainmurhag Hoiji 35:205-210(1999)
Cloning and Expression of zot gene from Vibrio cholerae.Zhi-Yong H., Wei-Jie Z., Xiang-Fu W. Kan B., Liu Y.Q., Qi G.M., Gao S.Y. DNA sequence of both chromosomes of the cholera pathogen Vibrio cholerae.Heidelberg J.F., Eisen J.A., Nelson W.C., Clayton R.A., Gwinn M.L., Dodson R.J., Haft D.H., Hickey E.K., Peterson J.D., Umayam L.A., Gill S.R., Nelson K.E., Read T.D., Tettelin H., Richardson D.L., Ermolaeva M.D., Vamathevan J.J., Bass S., Qin H., Dragoi I., Sellers P., McDonald L.A., Utterback T.R., Fleischmann R.D., Nierman W.C., White O., Salzberg S.L., Smith H.O., Colwell R.R., Mekalanos J.J., Venter J.C., Fraser C.M.Nature 406:477-483(2000)
Vibrio cholerae produces a second enterotoxin, which affects intestinal tight junctions.Fasano A., Baudry B., Pumplin D.W., Wasserman S.S., Tall B.D., Ketley J.M., Kaper J.B.Proc. Natl. Acad. Sci. U.S.A. 88:5242-5246(1991)
⇄⧉products_description => string (136) "Increases the permeability of the small intestine mucosa by affecting the st...
$value->a['products_description']
Increases the permeability of the small intestine mucosa by affecting the structure of intercellular tight junctions (zonula occludens).
⇄⧉products_references => string (1218) "Cloning of a gene (zot) encoding a new toxin produced by Vibrio cholerae.Bau...
$value->a['products_references']
Cloning of a gene (zot)
encoding a new toxin produced by Vibrio cholerae.Baudry B., Fasano A., Ketley J., Kaper J.B.Infect. Immun. 60:428-434(1992)
Cloning and nucleotide sequence analysis of the virulence gene cassette from Vibrio cholerae KNIH002 isolated in Korea.Shin H.J., Park Y.C., Kim Y.C.Misainmurhag Hoiji 35:205-210(1999)
Cloning and Expression of zot gene from Vibrio cholerae.Zhi-Yong H., Wei-Jie Z., Xiang-Fu W. Kan B., Liu Y.Q., Qi G.M., Gao S.Y. DNA sequence of both chromosomes of the cholera pathogen Vibrio cholerae.Heidelberg J.F., Eisen J.A., Nelson W.C., Clayton R.A., Gwinn M.L., Dodson R.J., Haft D.H., Hickey E.K., Peterson J.D., Umayam L.A., Gill S.R., Nelson K.E., Read T.D., Tettelin H., Richardson D.L., Ermolaeva M.D., Vamathevan J.J., Bass S., Qin H., Dragoi I., Sellers P., McDonald L.A., Utterback T.R., Fleischmann R.D., Nierman W.C., White O., Salzberg S.L., Smith H.O., Colwell R.R., Mekalanos J.J., Venter J.C., Fraser C.M.Nature 406:477-483(2000)
Vibrio cholerae produces a second enterotoxin, which affects intestinal tight junctions.Fasano A., Baudry B., Pumplin D.W., Wasserman S.S., Tall B.D., Ketley J.M., Kaper J.B.Proc. Natl. Acad. Sci. U.S.A. 88:5242-5246(1991)
⇄⧉products_description => string (136) "Increases the permeability of the small intestine mucosa by affecting the st...
$value->d['products_description']
Increases the permeability of the small intestine mucosa by affecting the structure of intercellular tight junctions (zonula occludens).
⇄⧉products_references => string (1218) "Cloning of a gene (zot) encoding a new toxin produced by Vibrio cholerae.Bau...
$value->d['products_references']
Cloning of a gene (zot)
encoding a new toxin produced by Vibrio cholerae.Baudry B., Fasano A., Ketley J., Kaper J.B.Infect. Immun. 60:428-434(1992)
Cloning and nucleotide sequence analysis of the virulence gene cassette from Vibrio cholerae KNIH002 isolated in Korea.Shin H.J., Park Y.C., Kim Y.C.Misainmurhag Hoiji 35:205-210(1999)
Cloning and Expression of zot gene from Vibrio cholerae.Zhi-Yong H., Wei-Jie Z., Xiang-Fu W. Kan B., Liu Y.Q., Qi G.M., Gao S.Y. DNA sequence of both chromosomes of the cholera pathogen Vibrio cholerae.Heidelberg J.F., Eisen J.A., Nelson W.C., Clayton R.A., Gwinn M.L., Dodson R.J., Haft D.H., Hickey E.K., Peterson J.D., Umayam L.A., Gill S.R., Nelson K.E., Read T.D., Tettelin H., Richardson D.L., Ermolaeva M.D., Vamathevan J.J., Bass S., Qin H., Dragoi I., Sellers P., McDonald L.A., Utterback T.R., Fleischmann R.D., Nierman W.C., White O., Salzberg S.L., Smith H.O., Colwell R.R., Mekalanos J.J., Venter J.C., Fraser C.M.Nature 406:477-483(2000)
Vibrio cholerae produces a second enterotoxin, which affects intestinal tight junctions.Fasano A., Baudry B., Pumplin D.W., Wasserman S.S., Tall B.D., Ketley J.M., Kaper J.B.Proc. Natl. Acad. Sci. U.S.A. 88:5242-5246(1991)
⇄⧉products_description => string (136) "Increases the permeability of the small intestine mucosa by affecting the st...
$value[0]['_source']['products_description']
Increases the permeability of the small intestine mucosa by affecting the structure of intercellular tight junctions (zonula occludens).
⇄⧉products_references => string (1218) "Cloning of a gene (zot) encoding a new toxin produced by Vibrio cholerae.Bau...
$value[0]['_source']['products_references']
Cloning of a gene (zot)
encoding a new toxin produced by Vibrio cholerae.Baudry B., Fasano A., Ketley J., Kaper J.B.Infect. Immun. 60:428-434(1992)
Cloning and nucleotide sequence analysis of the virulence gene cassette from Vibrio cholerae KNIH002 isolated in Korea.Shin H.J., Park Y.C., Kim Y.C.Misainmurhag Hoiji 35:205-210(1999)
Cloning and Expression of zot gene from Vibrio cholerae.Zhi-Yong H., Wei-Jie Z., Xiang-Fu W. Kan B., Liu Y.Q., Qi G.M., Gao S.Y. DNA sequence of both chromosomes of the cholera pathogen Vibrio cholerae.Heidelberg J.F., Eisen J.A., Nelson W.C., Clayton R.A., Gwinn M.L., Dodson R.J., Haft D.H., Hickey E.K., Peterson J.D., Umayam L.A., Gill S.R., Nelson K.E., Read T.D., Tettelin H., Richardson D.L., Ermolaeva M.D., Vamathevan J.J., Bass S., Qin H., Dragoi I., Sellers P., McDonald L.A., Utterback T.R., Fleischmann R.D., Nierman W.C., White O., Salzberg S.L., Smith H.O., Colwell R.R., Mekalanos J.J., Venter J.C., Fraser C.M.Nature 406:477-483(2000)
Vibrio cholerae produces a second enterotoxin, which affects intestinal tight junctions.Fasano A., Baudry B., Pumplin D.W., Wasserman S.S., Tall B.D., Ketley J.M., Kaper J.B.Proc. Natl. Acad. Sci. U.S.A. 88:5242-5246(1991)
⇄⧉search_terms => string (1306) "aaa18587 e coli or yeast baculovirus mammalian cell greater equal to 85 puri...
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aaa18587 e coli or yeast baculovirus mammalian cell greater equal to 85 purity as determined by sds page lyophilized liquid format be during the manufacturing process aaa18587_sds msifihhgapgsyktsgalwlrllpaiksgrhiitnvrglnlermakylkmdvsdisiefidtdhpdgrltmarfwhwarkdaflfidecgriwpprltvtnlkaldtppdlvaedrpesfevafdmhrhhgwdiclttpniakvhnmireaaeigyrhfnratvglgakftltthdaansgqmdshaltrqvkkipspifkmyastttgkardtmagtalwkdrkilflfgmvflmfsysfyglhdnpiftggndatieseqsepqskatvgnavgskavapasfgfcigrlcvqdgfvtvgderyrlvdnldipyrglwatghhiykdtltvffetesgsvptelfassyrykvlplpdfnhfvvfdtfaaqalwvevkrglpiktendkkglnsif
recombinant protein zona occludens toxin vibrio cholerae serotype o1 zot zonular vc1458 46.9 kda zot_vibch 15641469 np_231101.1 p38442 nc_002505.1 q9l7q6 q9r3v6 microbiology production note special offer host expressed is manufactured from a stock plasmid containing gene colihost stocked in different unit sizes ranging small 10 ug large 1 mg bulk inventory also available has been ordered over and again researchers stood test of time both robust important target for research community it part our new program make most popular targets corresponding hosts expanded with quick processing select fastest delivery among all please contact technical support team email [email protected] more details to85 small10 large1
⇄⧉specificity => string (179) "This assay has high sensitivity and excellent specificity for detection of h...
$value[1]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of human ZO1. No significant cross-reactivity or interference between human ZO1 and analogues was observed.
⇄purity => string (3) "N/A"
$value[1]['_source']['purity']
⇄form => string (3) "N/A"
$value[1]['_source']['form']
⇄concentration => string (3) "N/A"
$value[1]['_source']['concentration']
⇄⧉storage_stability => string (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[1]['_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[1]['_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 tight junction protein 1 (ZO1) ELISA Kit; DKFZp686M05161; MGC133289; ZO-1; tight junction protein 1; tight junction protein ZO-1; zona occludens 1; zonula occludens 1 protein; tight junction protein 1 (zona occludens 1)
⇄products_gene_name => string (4) "TJP1"
$value[1]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[1]['_source']['products_gene_name_syn']
⇄⧉products_description => string (727) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value[1]['_source']['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for ZO1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any ZO1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for ZO1 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 ZO1 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[1]['_source']['products_references']
⇄⧉products_related_diseases => string (208) "Inflammation||197!!Disease Models, Animal||153!!Nervous System Diseases||136...
$value[1]['_source']['products_related_diseases']
Inflammation||197!!Disease Models, Animal||153!!Nervous System Diseases||136!!Necrosis||127!!Brain Diseases||124!!Cardiovascular Diseases||105!!Edema||68!!Kidney Diseases||65!!Fibrosis||42!!Liver Diseases||42
⇄products_categories => string (3) "N/A"
$value[1]['_source']['products_categories']
⇄ncbi_full_name => string (37) "tight junction protein ZO-1 isoform a"
$value[1]['_source']['ncbi_full_name']
⇄ncbi_full_name_syn => string (24) "tight junction protein 1"
$value[1]['_source']['ncbi_full_name_syn']
⇄ncbi_symbol => string (4) "TJP1"
$value[1]['_source']['ncbi_symbol']
⇄ncbi_symbol_syn => string (4) "ZO-1"
$value[1]['_source']['ncbi_symbol_syn']
⇄ncbi_protein_info => string (73) "tight junction protein ZO-1; zona occludens 1; zonula occludens 1 protein"
⇄⧉search_terms => string (576) "aaa15065 human this assay has high sensitivity and excellent specificity for...
$value[1]['_source']['search_terms']
aaa15065 human this assay has high sensitivity and excellent specificity for detection of zo1 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa15065_td elisa kit tight junction protein 1 zona occludens dkfzp686m05161 mgc133289 zo zonula tjp1 isoform a 195,459 da zo1_human 116875767 np_003248.3 q07157 nm_003257.4 q2nkp3 q4zgj6 b4e3k1 601009 samples serum plasma cell culture supernates lysates type quantitative sandwich range 15.6 pg ml 1000 < 3.9 intra precision within an cv protein1 <3.9
⇄⧉products_description => string (670) "Intended Uses: This CHOLERA TOXIN ELISA kit is intended Laboratory for Resea...
$value[2]['_source']['products_description']
Intended Uses: This CHOLERA TOXIN ELISA kit is intended Laboratory for Research use only. The Stop Solution changes the color from blue to yellow and the intensity of the color is measured at 450 nm using a spectrophotometer. In order to measure the concentration of CHOLERA TOXIN in the sample, this CHOLERA TOXIN ELISA Kit includes a set of calibration standards. The calibration standards are assayed at the same time as the samples and allow the operator to produce a standard curve of Optical Density versus CHOLERA TOXIN concentration. The concentration of CHOLERA TOXIN in the samples is then determined by comparing the O.D. of the samples to the standard curve.
⇄⧉sp_protein_name_syn => string (232) "Cholera enterotoxin, A chainCleaved into the following 2 chains:Cholera ente...
$value[2]['_source']['sp_protein_name_syn']
Cholera enterotoxin, A chainCleaved into the following 2 chains:Cholera enterotoxin subunit A1 (EC:2.4.2.-)Alternative name(s):Cholera enterotoxin A1 chain; Cholera enterotoxin alpha chain; NAD(+)--diphthamide ADP-ribosyltransferase
⇄sp_gene_name => string (4) "ctxA"
$value[2]['_source']['sp_gene_name']
⇄sp_gene_name_syn => string (4) "toxA"
$value[2]['_source']['sp_gene_name_syn']
⇄sp_entry_name => string (10) "CHTA_VIBCH"
$value[2]['_source']['sp_entry_name']
⇄sp_mim => string (3) "N/A"
$value[2]['_source']['sp_mim']
⇄sp_interactions => string (3) "N/A"
$value[2]['_source']['sp_interactions']
⇄products_url => string (3) "N/A"
$value[2]['_source']['products_url']
⇄products_viewed => string (1) "0"
$value[2]['_source']['products_viewed']
⇄⧉search_terms => string (414) "aaa23663 human typical testing data standard curve for reference only aaa236...
$value[2]['_source']['search_terms']
aaa23663 human typical testing data standard curve for reference only aaa23663_sc elisa kit cholera toxin enterotoxin subunit a vc1457 chaincleaved into the following 2 chains:cholera a1 ec:2.4.2 alternative name s chain alpha nad + diphthamide adp ribosyltransferase ctxa toxa chta_vibch 15641468 np_231100.1 p01555 sensitivity 1 pg ml intra assay precision cv less than 15 inter is following2 sensitivity1 than15
⇄⧉products_description => string (1098) "Intended Uses: The Clostridium tetani toxin IgG ELISA is intended for the de...
$value[3]['_source']['products_description']
Intended Uses: The Clostridium tetani toxin IgG ELISA is intended for the determination of IgG class antibodies against Clostridium tetani toxin in human serum or plasma (citrate, heparin). For research use only -<br><br>Principle of the Assay: The immunoenzymatic determination of specific antibodies is based on the ELISA (Enzyme-linked Immunosorbent Assay) technique. Microtiterplates are coated with specific antigens to bind corresponding antibodies of the sample. After washing the wells to remove all unbound sample material a horseradish peroxidase (HRP) labelled conjugate is added. This conjugate binds to the captured antibodies. In a second washing step unbound conjugate is removed. The immune complex formed by the bound conjugate is visualized by adding Tetramethylbenzidine (TMB) substrate which gives a blue reaction product. The intensity of this product is proportional to the amount of specific antibodies in the sample. Sulphuric acid is added to stop the reaction. This produces a yellow endpoint colour. Absorbance at 450/620 nm is read using an ELISA Microtiterplate reader.
aaa14207 human elisa kit colstridium tetani toxin igg infectious disease immunology research assays assay categories samples serum or plasma citrate heparin detection range 0.01 iu ml 1 ml1
⇄⧉products_description => string (398) "Tetanus toxin acts by inhibiting neurotransmitter release. It binds to perip...
$value[4]['_source']['products_description']
Tetanus toxin acts by inhibiting neurotransmitter release. It binds to peripheral neuronal synapses, is internalized and moves by retrograde transport up the axon into the spinal cord where it can move between postsynaptic and presynaptic neurons. It inhibits neurotransmitter release by acting as a zinc endopeptidase that catalyzes the hydrolysis of the '76-Gln-|-Phe-77' bond of synaptobrevin-2.
⇄⧉products_references => string (1805) "Tetanus toxin primary structure, expression in E. coli, and homology with bo...
$value[4]['_source']['products_references']
Tetanus toxin
primary structure, expression in E. coli, and homology with botulinum toxins.Eisel U., Jarausch W., Goretzki K., Henschen A., Engels J., Weller U., Hudel M., Habermann E., Niemann H.EMBO J. 5:2495-2502(1986)
The complete nucleotide sequence of tetanus toxin.Fairweather N.F., Lyness V.A.Nucleic Acids Res. 14:7809-7812(1986)
The genome sequence of Clostridium tetani, the causative agent of tetanus disease.Brueggemann H., Baeumer S., Fricke W.F., Wiezer A., Liesegang H., Decker I., Herzberg C., Martinez-Arias R., Merkl R., Henne A., Gottschalk G.Proc. Natl. Acad. Sci. U.S.A. 100:1316-1321(2003)
Cloning, nucleotide sequencing, and expression of tetanus toxin fragment C in Escherichia coli.Fairweather N.F., Lyness V.A., Pickard D.J., Allen G., Thomson R.O.J. Bacteriol. 165:21-27(1986)
Arrangement of disulfide bridges and positions of sulfhydryl groups in tetanus toxin.Krieglstein K., Henschen A., Weller U., Habermann E.Eur. J. Biochem. 188:39-45(1990)
Limited proteolysis of tetanus toxin. Relation to activity and identification of cleavage sites.Krieglstein K.G., Henschen A.H., Weller U., Habermann E.Eur. J. Biochem. 202:41-51(1991)
Tetanus toxin is a zinc protein and its inhibition of neurotransmitter release and protease activity depend on zinc.Schiavo G., Poulain B., Rossetto O., Benfenati F., Tauc L., Montecucco C.EMBO J. 11:3577-3583(1992)
Tetanus and botulinum-B neurotoxins block neurotransmitter release by proteolytic cleavage of synaptobrevin.Schiavo G., Benfenati F., Poulain B., Rossetto O., de Laureto P.P., Dasgupta B.R., Montecucco C.Nature 359:832-835(1992)
Structure of the receptor binding fragment HC of tetanus neurotoxin.Umland T.C., Wingert L.M., Swaminathan S., Furey W.F. Jr., Schmidt J.J., Sax M.Nat. Struct. Biol. 4:788-792(1997)
Disease Pathway||1268854!!Infectious Disease Pathway||1269056!!Neurotoxicity Of Clostridium Toxins Pathway||1269145!!Toxicity Of Tetanus Toxin (TeNT) Pathway||1269149!!Uptake And Actions Of Bacterial Toxins Pathway||1269144
⇄⧉search_terms => string (1342) "aaa18711 e coli or yeast baculovirus mammalian cell greater equal to 85 puri...
$value[4]['_source']['search_terms']
aaa18711 e coli or yeast baculovirus mammalian cell greater equal to 85 purity as determined by sds page lyophilized liquid format be during the manufacturing process aaa18711_sds pitinnfrysdpvnndtiimmeppyckgldiyykafkitdriwivperyefgtkpedfnppssliegaseyydpnylrtdsdkdrflqtmvklfnriknnvagealldkiinaipylgnsyslldkfdtnsnsvsfnlleqdpsgattksamltnliifgpgpvlnknevrgivlrvdnknyfpcrdgfgsimqmafcpeyvptfdnvienitsltigkskyfqdpalllmhelihvlhglygmqvssheiipskqeiymqhtypisaeelftfggqdanlisidikndlyektlndykaianklsqvtscndpnididsykqiyqqkyqfdkdsngqyivnedkfqilynsimygfteielgkkfniktrlsyfsmnhdpvkipnllddtiyndtegfnieskdlkseykgqnmrvntnafrnvdgsglvskliglckkiipptnirenlynrta
recombinant protein tetanus toxin tetx clostridium tetani partial tentoxylysin ctc_rs14060 66.3 kda chain l h tetx_clote 499413369 wp_011100836.1 p04958 production note special offer host expressed is manufactured from a stock plasmid containing gene colihost stocked in different unit sizes ranging small 10 ug large 1 mg bulk inventory also available has been ordered over and again researchers stood test of time both robust important target for research community it part our new program make most popular targets corresponding hosts expanded with quick processing select fastest delivery among all please contact technical support team email [email protected] more details to85 small10 large1
⇄⧉products_description => string (232) "Has serine protease-like properties and binds to the skin protein profilaggr...
$value[5]['_source']['products_description']
Has serine protease-like properties and binds to the skin protein profilaggrin. Cleaves substrates after acidic residues. Exfoliative toxins cause impetigous diseases commonly referred as staphylococcal scalded skin syndrome (SSSS).
⇄⧉products_references => string (1439) "Sequence determination and comparison of the exfoliative toxin A and toxin B...
$value[5]['_source']['products_references']
Sequence determination and comparison of the exfoliative toxin A and toxin B genes from Staphylococcus aureus.Lee C.Y., Schmidt J.J., Johnson-Winegar A.D., Spero L., Iandolo J.J.J. Bacteriol. 169:3904-3909(1987)
Nucleotide sequence of the epidermolytic toxin A gene of Staphylococcus aureus.O'Toole P.W., Foster T.J.J. Bacteriol. 169:3910-3915(1987)
DNA sequencing of the eta gene coding for staphylococcal exfoliative toxin serotype A.Sakurai S., Suzuki H., Kondo I.J. Gen. Microbiol. 134:711-717(1988)
The reactive serine residue of epidermolytic toxin A.Bailey C.J., Smith T.P.Biochem. J. 269:535-537(1990)
The epidermolytic toxins are serine proteases.Dancer S.J., Garrat R., Saldanha J., Jhoti H., Evans R.FEBS Lett. 268:129-132(1990)
The role of the serine protease active site in the mode of action of epidermolytic toxin of Staphylococcus aureus.Redpath M.B., Foster T.J., Bailey C.J.FEMS Microbiol. Lett. 65:151-155(1991)
The structure of the superantigen exfoliative toxin A suggests a novel regulation as a serine protease.Vath G.M., Earhart C.A., Rago J.V., Kim M.H., Bohach G.A., Schlievert P.M., Ohlendorf D.H.Biochemistry 36:1559-1566(1997)
The structure of Staphylococcus aureus epidermolytic toxin A, an atypic serine protease, at 1.7-A resolution.Cavarelli J., Prevost G., Bourguet W., Moulinier L., Chevrier B., Delagoutte B., Bilwes A., Mourey L., Rifai S., Piemont Y., Moras D.Structure 5:813-824(1997)
⇄⧉search_terms => string (1104) "aaa18686 e coli or yeast baculovirus mammalian cell greater equal to 85 puri...
$value[5]['_source']['search_terms']
aaa18686 e coli or yeast baculovirus mammalian cell greater equal to 85 purity as determined by sds page lyophilized liquid format be during the manufacturing process aaa18686_sds evsaeeikkheekwnkyygvnafnlpkelfskvdekdrqkypyntignvfvkgqtsatgvligkntvltnrhiakfangdpskvsfrpsintddngntetpygeyevkeilqepfgagvdlalirlkpdqngvslgdkispakigtsndlkdgdkleligypfdhkvnqmhrseielttlsrglryygftvpgnsgsgifnsngelvgihsskvshldrehqinygvgignyvkriinekne
recombinant protein exfoliative toxin a staphylococcus aureus eta epidermolytic 30.9 kda eta_staau 446988525 wp_001065781.1 p09331 production note special offer host expressed is manufactured from stock plasmid containing gene colihost stocked in different unit sizes ranging small 10 ug large 1 mg bulk inventory also available has been ordered over and again researchers stood test of time both robust important target for research community it part our new program make most popular targets corresponding hosts expanded with quick processing select fastest delivery among all please contact technical support team email [email protected] more details to85 small10 large1
⇄⧉specificity => string (171) "The specificity is defined as the probability of the assay of scoring negati...
$value[6]['_source']['specificity']
The specificity is defined as the probability of the assay of scoring negative in the absence of the specific analyte. It is 100% (95% confidence interval: 89.42% - 100%).
⇄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 (132) "Store the kit at 2-8 degree C. The opened reagents are stable up to the expi...
$value[6]['_source']['storage_stability']
Store the kit at 2-8 degree C. The opened reagents are stable up to the expiry date stated on the label when stored at 2-8 degree C.
⇄⧉products_description => string (1154) "Principle of the Assay: The immunoenzymatic determination of specific antibo...
$value[6]['_source']['products_description']
Principle of the Assay: The immunoenzymatic determination of specific antibodies is based on the ELISA (Enzyme-linked Immunosorbent Assay) technique. Microtiterplates are coated with specific antigens to bind corresponding antibodies of the sample. After washing the wells to remove all unbound sample material a horseradish peroxidase (HRP) labelled conjugate is added. This conjugate binds to the captured antibodies. In a second washing step unbound conjugate is removed. The immune complex formed by the bound conjugate is visualized by adding Tetramethylbenzidine (TMS) substrate which gives a blue reaction product. The intensity of this product is proportional to the amount of specific antibodies in the sample. Sulphuric aCid is added to stop the reaction. This produces a yellow endpoint colour. Absorbance at 4501620 nm is read using an ELISA Microtiterplate reader.<br><br>Intended Uses: The Corynebacterium diphtheriae toxin IgG ELISA is intended for the determination of IgG class antibodies against Corynebacterium dlphtheriae toxin in human serum or plasma (citrate, heparin). For Research Use Only - Not for Use in Diagnostic Procedures.
⇄products_references => string (3) "N/A"
$value[6]['_source']['products_references']
⇄products_related_diseases => string (3) "N/A"
$value[6]['_source']['products_related_diseases']
⇄products_categories => string (3) "N/A"
$value[6]['_source']['products_categories']
⇄ncbi_full_name => string (3) "N/A"
$value[6]['_source']['ncbi_full_name']
⇄ncbi_full_name_syn => string (3) "N/A"
$value[6]['_source']['ncbi_full_name_syn']
⇄ncbi_symbol => string (3) "N/A"
$value[6]['_source']['ncbi_symbol']
⇄ncbi_symbol_syn => string (3) "N/A"
$value[6]['_source']['ncbi_symbol_syn']
⇄ncbi_protein_info => string (3) "N/A"
$value[6]['_source']['ncbi_protein_info']
⇄ncbi_chrom_loc => string (3) "N/A"
$value[6]['_source']['ncbi_chrom_loc']
⇄ncbi_gene_id => string (3) "N/A"
$value[6]['_source']['ncbi_gene_id']
⇄ncbi_mol_weight => string (3) "N/A"
$value[6]['_source']['ncbi_mol_weight']
⇄ncbi_pathways => string (3) "N/A"
$value[6]['_source']['ncbi_pathways']
⇄sp_protein_name => string (3) "N/A"
$value[6]['_source']['sp_protein_name']
⇄sp_protein_name_syn => string (3) "N/A"
$value[6]['_source']['sp_protein_name_syn']
⇄sp_gene_name => string (3) "N/A"
$value[6]['_source']['sp_gene_name']
⇄sp_gene_name_syn => string (3) "N/A"
$value[6]['_source']['sp_gene_name_syn']
⇄sp_entry_name => string (3) "N/A"
$value[6]['_source']['sp_entry_name']
⇄sp_mim => string (3) "N/A"
$value[6]['_source']['sp_mim']
⇄sp_interactions => string (3) "N/A"
$value[6]['_source']['sp_interactions']
⇄products_url => string (3) "N/A"
$value[6]['_source']['products_url']
⇄products_viewed => string (1) "0"
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⇄⧉search_terms => string (240) "aaa14224 the specificity is defined as probability of assay scoring negative...
$value[6]['_source']['search_terms']
aaa14224 the specificity is defined as probability of assay scoring negative in absence specific analyte it 100 95 confidence interval 89.42 elisa kit corynebacterium diphtheriae toxin igg samples human serum or plasma citrate heparin it100
⇄⧉specificity => string (185) "This assay has high sensitivity and excellent specificity for detection of h...
$value[7]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of human ANTXR1. No significant cross-reactivity or interference between human ANTXR1 and analogues was observed.
⇄purity => string (3) "N/A"
$value[7]['_source']['purity']
⇄form => string (3) "N/A"
$value[7]['_source']['form']
⇄concentration => string (3) "N/A"
$value[7]['_source']['concentration']
⇄⧉storage_stability => string (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[7]['_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[7]['_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 (739) "Principle of the Assay: This assay employs the quantitative sandwich enzyme ...
$value[7]['_source']['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for ANTXR1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any ANTXR1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for ANTXR1 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 ANTXR1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄⧉search_terms => string (649) "aaa18349 human this assay has high sensitivity and excellent specificity for...
$value[7]['_source']['search_terms']
aaa18349 human this assay has high sensitivity and excellent specificity for detection of antxr1 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa18349_td elisa kit anthrax toxin receptor 1 atr flj10601 flj11298 flj21776 tem8 2310008j16rik 2810405n18rik tumor endothelial marker 8 isoform 3 gapo 62,789 da antr1_human 16933553 np_060623.2 q9h6x2 nm_018153.3 q4zfv6 q53qd8 q96p02 q9nvp3 a8k7u8 j7k7g4 j7kf88 606410 samples serum plasma tissue homogenates type quantitative sandwich range 62.5 pg ml 4000 < 15.6 intra precision within an cv receptor1 marker8 isoform3
Assay Type||Quantitative Sandwich!!Samples||Serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids!!Detection Range||0.05-15ng/ml!!Sensitivity||0.028ng/ml
⇄⧉etc_term2 => string (403) "Intra-assay Precision||Intra-Assay Precision (Precision within an assay) Thr...
$value[8]['_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 (893) "Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (EL...
$value[8]['_source']['products_description']
Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (ELISA). The plate has been pre-coated with Chicken ZO-1 antibody. ZO-1 present in the sample is added and binds to antibodies coated on the wells. And then biotinylated Chicken ZO-1 Antibody is added and binds to ZO-1 in the sample. Then Streptavidin-HRP is added and binds to the Biotinylated ZO-1 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 Chicken ZO-1. 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 Chicken zonula occludens-1 (also known as ZO-1) in serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids.
⇄⧉search_terms => string (545) "aaa18989 chicken typical testing data standard curve for reference only aaa1...
$value[8]['_source']['search_terms']
aaa18989 chicken typical testing data standard curve for reference only aaa18989_sc elisa kit zonula occludens 1 zo tight junction protein tjp1 zo1 194,742 da zona 303710 baa03274.1 p39447 e9qk00 samples serum plasma cell culture supernates ascites tissue homogenates or other biological fluids assay type quantitative sandwich detection range 0.05 15ng ml sensitivity 0.028ng intra precision within an three of known concentration were tested on one plate to assess cv<8 inter between assays in separate cv = sd mean x 100 cv<10 occludens1 x100
Assay Type||Quantitative Sandwich!!Samples||Serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids!!Detection Range||25-1600ng/L!!Sensitivity||13.68ng/L
⇄⧉etc_term2 => string (403) "Intra-assay Precision||Intra-Assay Precision (Precision within an assay) Thr...
$value[9]['_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 (893) "Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (EL...
$value[9]['_source']['products_description']
Principle of the Assay: This kit is an Enzyme-Linked Immunosorbent Assay (ELISA). The plate has been pre-coated with Chicken ZO-2 antibody. ZO-2 present in the sample is added and binds to antibodies coated on the wells. And then biotinylated Chicken ZO-2 Antibody is added and binds to ZO-2 in the sample. Then Streptavidin-HRP is added and binds to the Biotinylated ZO-2 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 Chicken ZO-2. 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 Chicken zonula occludens-2 (also known as ZO-2) in serum, plasma, cell culture supernates, Ascites, tissue homogenates or other biological fluids.
⇄⧉products_description => string (828) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[10]['_source']['products_description']
Principle of the Assay: As mentioned above, this kit utilizes the Double Antibody Sandwich ELISA technique. The pre-coated antibody is an anti-Human TSST-1 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 (373) "aaa12493 human typical testing data standard curve for reference only aaa124...
$value[10]['_source']['search_terms']
aaa12493 human typical testing data standard curve for reference only aaa12493_sc elisa kit toxic shock syndrom toxin 1 tsst syndrome 26,306 da tst tsst_staau 136457 p06886.1 samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 100 ng ml 1.56 sensitivity up to 0.5 intra precision <= 8 inter 12 toxin1 range100 to0.5 <=8 inter12
⇄host => string (48) "E Coli or Yeast or Baculovirus or Mammalian Cell"
$value[12]['_source']['host']
⇄reactivity => string (3) "N/A"
$value[12]['_source']['reactivity']
⇄specificity => string (3) "N/A"
$value[12]['_source']['specificity']
⇄purity => string (57) "Greater or equal to 85% purity as determined by SDS-PAGE."
$value[12]['_source']['purity']
⇄⧉form => string (80) "Lyophilized or liquid (Format to be determined during the manufacturing proc...
$value[12]['_source']['form']
Lyophilized or liquid (Format to be determined during the manufacturing process)
⇄concentration => string (3) "N/A"
$value[12]['_source']['concentration']
⇄⧉storage_stability => string (195) "Store at -20 degrees C. For long-term storage, store at -20 degrees C or -80...
$value[12]['_source']['storage_stability']
Store at -20 degrees C. For long-term storage, store at -20 degrees C or -80 degrees C. Store working aliquots at 4 degrees C for up to one week. Repeated freezing and thawing is not recommended.
⇄⧉products_description => string (288) "Part of the tripartite complex that is required for the CDT activity. CdtB e...
$value[12]['_source']['products_description']
Part of the tripartite complex that is required for the CDT activity. CdtB exhibits a DNA-nicking endonuclease activity, and very probably causes DNA damage in intoxicated cells. This damage induces G2/M cell cycle arrest, chromatin fragmentation, cell distention and nucleus enlargement.
⇄⧉search_terms => string (1148) "aaa18773 e coli or yeast baculovirus mammalian cell greater equal to 85 puri...
$value[12]['_source']['search_terms']
aaa18773 e coli or yeast baculovirus mammalian cell greater equal to 85 purity as determined by sds page lyophilized liquid format be during the manufacturing process aaa18773_sds dltdfrvatwnlqgasatteskwninvrqlisgenavdilavqeagsppstavdtgtlipspgipvreliwnlstnsrpqqvyiyfsavdalggrvnlalvsnrradevfvlspvrqggrpllgirigndafftahaiamrnndapalveevynffrdsrdpvhqalnwmilgdfnrepadlemnltvpvrraseiispaaatqtsqrtldyavagnsvafrpsplqagivygarrtqissdhfpvgvsrr
recombinant protein cytolethal distending toxin subunit b cdtb escherichia cdt deoxyribonuclease ec=3.1 47.4 kda ec:3.1 cdtb_ecolx 57012651 q46669.1 q46669 species production note special offer host expressed is manufactured from a stock plasmid containing gene colihost stocked in different unit sizes ranging small 10 ug large 1 mg bulk inventory also available has been ordered over and again researchers stood test of time both robust important target for research community it part our new program make most popular targets corresponding hosts expanded with quick processing select fastest delivery among all please contact technical support team email [email protected] more details to85 small10 large1
⇄⧉specificity => string (379) "This assay has high sensitivity and excellent specificity for detection of T...
$value[13]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of TSST1. No significant cross-reactivity or interference between TSST1 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between TSST1 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 (1402) "Principle of the Assay: TSST1 ELISA kit applies the competitive enzyme immun...
$value[13]['_source']['products_description']
Principle of the Assay: TSST1 ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-TSST1 antibody and an TSST1-HRP conjugate. The assay sample and buffer are incubated together with TSST1-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 TSST1 concentration since TSST1 from samples and TSST1-HRP conjugate compete for the anti-TSST1 antibody binding site. Since the number of sites is limited, as more sites are occupied by TSST1 from the sample, fewer sites are left to bind TSST1-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The TSST1 concentration in each sample is interpolated from this standard curve.<br><br>Intended Uses: This TSST1 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human TSST1. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
⇄⧉search_terms => string (624) "aaa17193 human this assay has high sensitivity and excellent specificity for...
$value[13]['_source']['search_terms']
aaa17193 human this assay has high sensitivity and excellent specificity for detection of tsst1 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 aaa17193_sc elisa kit toxic shock syndrome toxin 1 tsst tst 26,447 da sav2011 q7a2n8_staam 15925001 np_372535.1 q7a2n8 nc_002758.2 samples serum plasma cell culture supernatants body fluid tissue homogenate type quantitative competitive 0.1 ng ml toxin1 competitive0.1
⇄⧉products_description => string (838) "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-Human Shiga Toxin 1 +2 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 (315) "aaa22774 human typical testing data standard curve for reference only aaa227...
$value[14]['_source']['search_terms']
aaa22774 human typical testing data standard curve for reference only aaa22774_sc elisa kit verotoxin 1 +2 shiga toxin samples serum plasma or cell culture supernatant assay type quantitative sandwich detection range 10 ng ml 0.156 sensitivity up to 0.05 intra precision <= 8 inter 12 verotoxin1 range10 <=8 inter12
⇄⧉specificity => string (183) "This assay has high sensitivity and excellent specificity for detection of h...
$value[15]['_source']['specificity']
This assay has high sensitivity and excellent specificity for detection of human SPAM1. No significant cross-reactivity or interference between human SPAM1 and analogues was observed.
⇄purity => string (3) "N/A"
$value[15]['_source']['purity']
⇄form => string (3) "N/A"
$value[15]['_source']['form']
⇄concentration => string (3) "N/A"
$value[15]['_source']['concentration']
⇄⧉storage_stability => string (129) "Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please ...
$value[15]['_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[15]['_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[15]['_source']['products_description']
Principle of the Assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for SPAM1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any SPAM1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for SPAM1 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 SPAM1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
⇄⧉search_terms => string (706) "aaa18205 human this assay has high sensitivity and excellent specificity for...
$value[15]['_source']['search_terms']
aaa18205 human this assay has high sensitivity and excellent specificity for detection of spam1 no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa18205_td elisa kit sperm adhesion molecule 1 ph 20 hyaluronidase zona pellucida binding hya1 hyal1 hyal3 hyal5 mgc26532 ph20 spag15 otthump00000211901 hyaluronoglucosaminidase surface protein isoform 2 hel s 96n hyal epididymis secretory li 57,848 da hyalp_human 291290979 np_001167515.1 p38567 nm_001174044.1 q8tc30 600930 samples serum plasma tissue homogenates urine type quantitative sandwich range 15.6 pg ml 1000 < 3.9 intra precision within an cv molecule1 isoform2 <3.9
⇄products_name => string (21) "Angiotensin I (Ang-I)"
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⇄products_name_oem => string (37) "Human Angiotensin I (Ang-I) ELISA Kit"
$value[17]['_source']['products_name_oem']
⇄products_name_syn => string (3) "N/A"
$value[17]['_source']['products_name_syn']
⇄products_gene_name => string (5) "Ang-I"
$value[17]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[17]['_source']['products_gene_name_syn']
⇄⧉products_description => string (827) "Principle of the Assay: As mentioned above, this kit utilizes the Double Ant...
$value[17]['_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 Ang-I 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 (649) "aaa12606 human no cross reaction with other factors typical testing data sta...
$value[17]['_source']['search_terms']
aaa12606 human no cross reaction with other factors typical testing data standard curve for reference only aaa12606_sc elisa kit angiotensin i ang angiotensinogen preproprotein serpin peptidase inhibitor clade a member 8 agt anhu serpina8 a8 ii pre alpha 1 antiproteinase antitrypsin serine or cysteine proteinase 53,154 da a8cleaved into the following chains:angiotensin 1alternative name s 10 iii iv angt_human 4557287 np_000020.1 p01019 nm_000029.3 q16358 q16359 q96f91 267430 samples serum plasma cell culture supernatant assay type quantitative sandwich detection range 1000 pg ml 15.6 sensitivity up to 5 intra precision member8 alpha1 s10 to5
⇄specificity => string (78) "Specifically recognize APOA1BP, 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.
⇄products_name_oem => string (50) "Human Apolipoprotein A-I-binding protein ELISA Kit"
$value[18]['_source']['products_name_oem']
⇄⧉products_name_syn => string (135) "APOA1BP/AIBP/YJEFN1/YjeF_N1/AI-BP/YjeF N-terminal domain-containing protein ...
$value[18]['_source']['products_name_syn']
APOA1BP/AIBP/YJEFN1/YjeF_N1/AI-BP/YjeF N-terminal domain-containing protein 1/Apolipoprotein A-I-binding protein ()/NAD (P)HX epimerase
⇄products_gene_name => string (7) "APOA1BP"
$value[18]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[18]['_source']['products_gene_name_syn']
⇄⧉products_description => string (1753) "Background: Apolipoprotein A-I-binding protein, also known as AIBP, is a pro...
$value[18]['_source']['products_description']
Background: Apolipoprotein A-I-binding protein, also known as AIBP, is a protein encoded by the APOA1BP gene. It interacts with apolipoprotein A-I (apoA-I), the major protein component of high-density lipoprotein (HDL) particles, and modulates its function. APOA1BP is involved in cholesterol metabolism and transport, particularly in the reverse cholesterol transport pathway, where it facilitates cholesterol efflux from peripheral tissues to the liver for excretion. APOA1BP has been implicated in the regulation of lipid metabolism, inflammation, and atherosclerosis. Studies have shown that APOA1BP expression is altered in various metabolic diseases, such as obesity, diabetes, and cardiovascular diseases, suggesting its potential as a therapeutic target for metabolic disorders.<br><br>Principle of the Assay: This kit was based on sandwich enzyme-linked immune-sorbent assay technology. Anti APOA1BP antibody was pre-coated onto the 96-well plate. The biotin conjugated anti APOA1BP 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 APOA1BP 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 APOA1BP 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 (569) "aaa17708 human this assay has high sensitivity and excellent specificity for...
$value[18]['_source']['search_terms']
aaa17708 human this assay has high sensitivity and excellent specificity for detection of apoa1bp no significant cross reactivity or interference between analogues was observed typical testing data standard curve reference only aaa17708_sc elisa kit apolipoprotein a i binding protein aibp yjefn1 yjef_n1 ai bp yjef n terminal domain containing 1 nad p hx epimerase 318054060 np_001187647.1 nm_001200718.1 samples serum plasma tissue homogenates other biological fluids type quantitative sandwich range 0.156 10ng ml 0.094ng intra precision cv<8 inter cv<10 containing1
⇄products_name_oem => string (33) "Human troponin I (Tn-I) 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 (4) "Tn-I"
$value[19]['_source']['products_gene_name']
⇄products_gene_name_syn => string (3) "N/A"
$value[19]['_source']['products_gene_name_syn']
⇄⧉products_description => string (826) "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-Human Tn-I 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 (285) "aaa22556 human typical testing data standard curve for reference only aaa225...
$value[19]['_source']['search_terms']
aaa22556 human typical testing data standard curve for reference only aaa22556_sc elisa kit troponin i tn 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 to5 <=8 inter12
