Elisa 96 Wells

Species Reactivity : Fish
UniProt :
Abbreviation : PRKRA
Alternative Names : DYT16; HSD14; PACT; RAX; protein activator of the interferon-induced protein kinase
Application :
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV :
Inter-AssayCV :
Recovery :
Sample Type : Serum, Plasma, Other biological fluids
Detection Method :
Analysis Method?? :
Test principle :
Product Overview :
Stability :

Volume : 96 Tests. Other Volumes are also available. Please Inquire.
Research topic : Immunology
Uniprot ID :
Species : Fish
Former Code : CSB-EL011050FI
Alias :
Product Type : ELISA Kit
Sample Type : serum, plasma, tissue homogenates
Detect Range : 20 pg/ml-4000 pg/ml
Sensitivity : 10 pg/ml.
Antigen Name : Interferon γ ,IFN-
Abbreviation : IFN-
Protein Biological Process 1 :
Protein Biological Process 2 :
Protein Biological Process 3 :
Assay Time : 1-5h
Sample Volume : 50-100 µL
Detection Wavelength : 450 nm
Delievery Date : 3-5 working days

Species Reactivity : Fish
UniProt : N/A
Abbreviation : IFNG
Alternative Names : IFB; IFF; IFNB; MGC96956; interferon beta
Application : ELISA
Range : 62.5-4000 pg/mL
Sensitivity : 37.5 pg/mL
Intra-AssayCV : ?4.6%
Inter-AssayCV : ?6.5%
Recovery : 1.02
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate IFNG in samples. An antibody specific for IFNG has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyIFNG present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for IFNG is added to the wells. After washing, Streptavidin conj µgated 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 IFNG bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview :
Stability : The stability of ELISA 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. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Fish
UniProt : N/A
Abbreviation : IGF1
Alternative Names : IGF1A; IGFI; OTTHUMP00000195084|ins µLin-like growth factor 1
Application : ELISA
Range : 31.25-2000 pg/mL
Sensitivity : 15.5 pg/mL
Intra-AssayCV : ?6.2%
Inter-AssayCV : ?9.2%
Recovery : 1.05
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate IGF1 in samples. An antibody specific for IGF1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyIGF1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for IGF1 is added to the wells. After washing, Streptavidin conj µgated 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 IGF1 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview :
Stability : The stability of ELISA 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. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Volume : 96 Tests. Other Volumes are also available. Please Inquire.
Research topic : Metabolism
Uniprot ID : P10764
Species : Fish
Former Code :
Alias : C11orf43, FLJ22066, FLJ44734, INSIGF, pp9974, OTTHUMP00000011018|OTTHUMP00000011157|ins µLin-like growth factor 2|ins µLin-like growth factor II|ins µLin-like growth factor type 2|putative ins µLin-like
Product Type : ELISA Kit
Sample Type : serum, plasma
Detect Range : 62.5 pg/ml-1000 pg/ml
Sensitivity : 31.25 pg/ml
Antigen Name : ins µLin-like growth factor 2 (somatomedin A)
Abbreviation : IGF2
Protein Biological Process 1 : Biosynthesis/Metabolism
Protein Biological Process 2 : glyconeogenesis and glycometabolism
Protein Biological Process 3 : Carbohydrate metabolism
Assay Time : 1-5h
Sample Volume : 50-100 µL
Detection Wavelength : 450 nm
Delievery Date : 5-7 working days

Species Reactivity : Fish
UniProt : N/A
Abbreviation : ISR
Alternative Names : N/A
Application : ELISA
Range : 50-1600 pg/mL
Sensitivity : 28 pg/mL
Intra-AssayCV : ?4.9%
Inter-AssayCV : ?7.9%
Recovery : 0.92
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate ISR in samples. An antibody specific for ISR has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyISR present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for ISR is added to the wells. After washing, Streptavidin conj µgated 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 ISR bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview :
Stability : The stability of ELISA 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. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Fish
UniProt : N/A
Abbreviation : INS
Alternative Names : N/A
Application : ELISA
Range : 15.6-1000 pg/mL
Sensitivity : 7.8 pg/mL
Intra-AssayCV : ?5.2%
Inter-AssayCV : ?7.5%
Recovery : 0.87
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate INS in samples. An antibody specific for INS has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyINS present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for INS is added to the wells. After washing, Streptavidin conj µgated 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 INS bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Ins µLin is a polypeptide hormone originating in the beta cells of the pancreas and serving as a principal reg µLator for the storage and production of carbohydrates. Its secretion is normally stim µLated by increases in the amount of glucose in circ µLation. This leads to higher ins µLin levels and more rapid tissueassimilation of glucose followed by a decline in the ins µLin level as the glucose level subsides. In a number of conditions, notably ins µLinoma and diabetes, this relationship is impaired. Ins µLin tends to circ µLate at inappropriately high levels in patients with ins µLin-secreting pancreatic tumors; such tumors can thus be a cause of hypoglycemia. Accordingly, ins µLin immunoassays used sometimes in connection with provocative doses of tolbutamide or calcium play an essential role in the identification (and localization) of ins µLinomas.
Stability : The stability of ELISA 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. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Fish
UniProt :
Abbreviation : INHA
Alternative Names : A-inhibin subunit|inhibin alpha subunit
Application :
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV :
Inter-AssayCV :
Recovery :
Sample Type : Serum, Plasma, Other biological fluids
Detection Method :
Analysis Method?? :
Test principle :
Product Overview :
Stability :

Species Reactivity : Fish
UniProt : N/A
Abbreviation : IgM
Alternative Names : N/A
Application : ELISA
Range : 1.56-100 ?g/mL
Sensitivity : 0.75 ?g/mL
Intra-AssayCV : ?6.8%
Inter-AssayCV : ?8.8%
Recovery : 1.03
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate IgM in samples. An antibody specific for IgM has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyIgM present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for IgM is added to the wells. After washing, Streptavidin conj µgated 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 IgM bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview :
Stability :

Species Reactivity : Fish
UniProt :
Abbreviation : IgG
Alternative Names : N/A
Application :
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV :
Inter-AssayCV :
Recovery :
Sample Type : Serum, Plasma, Other biological fluids
Detection Method :
Analysis Method?? :
Test principle :
Product Overview :
Stability :

Species Reactivity : Fish
UniProt :
Abbreviation : IgE
Alternative Names : N/A
Application :
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV :
Inter-AssayCV :
Recovery :
Sample Type : Serum, Plasma, Other biological fluids
Detection Method :
Analysis Method?? :
Test principle :
Product Overview :
Stability :

Species Reactivity : Fish
UniProt :
Abbreviation : IgA
Alternative Names : N/A
Application :
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV :
Inter-AssayCV :
Recovery :
Sample Type : Serum, Plasma, Other biological fluids
Detection Method :
Analysis Method?? :
Test principle :
Product Overview :
Stability :

Species Reactivity : Fish
UniProt :
Abbreviation : SIX1
Alternative Names : BOS3; DFNA23; TIP39; sine oc µLis homeobox homolog 1
Application :
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV :
Inter-AssayCV :
Recovery :
Sample Type : Serum, Plasma, Other biological fluids
Detection Method :
Analysis Method?? :
Test principle :
Product Overview :
Stability :

Species Reactivity : Fish
UniProt : N/A
Abbreviation : HIS
Alternative Names : AKR1B10; AKR1B12; Aldose Reductase Like 1; HSI; ALDRLn; Aldo-Keto Reductase Family 1Member B10; Aldose Reductase-Related Protein; Small Intestine Reductase
Application : ELISA
Range : 0.625-40 ng/mL
Sensitivity : 0.31 ng/mL
Intra-AssayCV : ?6.1%
Inter-AssayCV : ?11.6%
Recovery : 1.07
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate HIS in samples. An antibody specific for HIS has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyHIS present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for HIS is added to the wells. After washing, Streptavidin conj µgated 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 HIS bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : Aldose reductase (AR) is an NADPH-dependent enzyme that was first identified by its ability to reduce glucose to sorbitol. The deduced 316-amino acid AKR1B10 protein shares 71% amino acid identity with AR. Northern blot analysis revealed that AKR1B10 is overexpressed in 54% of HCCs, while AR is overexpressed in 29% of HCCs. Northern blot analysis of normal tissues showed that unlike the ubiquitously expressed AR, AKR1B10 is expressed most abundantly in small intestine and colon, with lower levels in liver, thymus, prostate, testis, and skeletal muscle. AR and ARL1 reduce a similar spectrum of aromatic and aliphatic aldehyde substrates.Highest expression of AKR1B10 in adrenal gland, with modest expression in stomach, placenta, small intestine, and pancreas, and lower expression in all other tissues tested.
Stability : The stability of ELISA 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. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Fish
UniProt : N/A
Abbreviation : hs-CRP
Alternative Names : N/A
Application : ELISA
Range : 3.125-200 ng/mL
Sensitivity : 1.2 ng/mL
Intra-AssayCV : ?5.3%
Inter-AssayCV : ?8.8%
Recovery : 0.95
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate hs-CRP in samples. An antibody specific for hs-CRP has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyhs-CRP present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for hs-CRP is added to the wells. After washing, Streptavidin conj µgated 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 hs-CRP bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview :
Stability : The stability of ELISA 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. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Fish
UniProt : N/A
Abbreviation : HDL
Alternative Names : N/A
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?6.2%
Inter-AssayCV : ?98%
Recovery : 0.97
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate HDL in samples. An antibody specific for HDL has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyHDL present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for HDL is added to the wells. After washing, Streptavidin conj µgated 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 HDL bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : High-density lipoproteins (HDL) form a class of lipoproteins, varying somewhat in their Volume (8–11 nm in diameter), that carry cholesterol from the bodys tissues to the liver. About thirty percent of blood cholesterol is carried by HDL.HDL is the smallest of the lipoprotein particles. They are the densest because they contain the highest proportion of protein.It is hypothesised that HDL can remove cholesterol from atheroma within arteries and transport it back to the liver for excretion or re-utilization—which is the main reason why HDL-bound cholesterol is sometimes called "good cholesterol", or HDL-C. A high level of HDL-C seems to protect against cardiovasc µLar diseases, and low HDL cholesterol levels (less than 40 mg/dL) increase the risk for heart disease. When measuring cholesterol, any contained in HDL particles is considered as protection to the bodys cardiovasc µLar health, in contrast to "bad" LDL cholesterol.
Stability : The stability of ELISA 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. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).

Species Reactivity : Fish
UniProt :
Abbreviation : HK1
Alternative Names : HK1-ta; HK1-tb; HK1-tc; HKI; HXK1; brain form hexokinase|glycolytic enzyme
Application :
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV :
Inter-AssayCV :
Recovery :
Sample Type : Serum, Plasma, Other biological fluids
Detection Method :
Analysis Method?? :
Test principle :
Product Overview :
Stability :

Volume : 96 Tests. Other Volumes are also available. Please Inquire.
Research topic : Cancer
Uniprot ID : P14210
Species : Fish
Former Code : CSB-EL010327FI
Alias : DFNB39, F-TCF, HGFB, HPTA, SF, OTTHUMP00000206710|fibroblast-derived tumor cytotoxic factor|hepatocyte growth factor|lung fibroblast-derived mitogen
Product Type : ELISA Kit
Sample Type :
Detect Range :
Sensitivity : 145 pg/ml
Antigen Name : hepatocyte growth factor(HGF)
Abbreviation : HGF
Protein Biological Process 1 :
Protein Biological Process 2 :
Protein Biological Process 3 :
Assay Time : 1-5h
Sample Volume : 50-100 µL
Detection Wavelength : 450 nm
Delievery Date : 3-5 working days

Species Reactivity : Fish
UniProt :
Abbreviation : NOX1
Alternative Names : RP1-146H21.1; GP91-2; MOX1; NOH-1; NOH1; NADPH oxidase 1 variant NOH-1L|NADPH oxidase homolog-1|mitogenic oxidase (pyridine nucleotide-dependent superoxide-generating)
Application :
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV :
Inter-AssayCV :
Recovery :
Sample Type : Serum, Plasma, Other biological fluids
Detection Method :
Analysis Method?? :
Test principle :
Product Overview :
Stability :

Species Reactivity : Fish
UniProt : N/A
Abbreviation : HSP-90
Alternative Names : HSP90; FLJ31884; HSP86; HSP89A; HSP90A; HSP90N; HSPC1; HSPCA; HSPCAL1; HSPCAL4; HSPN; Hsp89; Hsp90; LAP2; heat shock 90kD protein 1; alpha|heat shock 90kD protein 1; alpha-like 4|heat shock 90kD protein;
Application : ELISA
Range : 0.5-8 ng/mL
Sensitivity : 0.255 ng/mL
Intra-AssayCV : ?4.1%
Inter-AssayCV : ?9.2%
Recovery : 0.88
Sample Type : Serum, Plasma, Other biological fluids
Detection Method : Sandwich
Analysis Method?? : Quantitive
Test principle : This assay employs a two-site sandwich ELISA to quantitate HSP-90 in samples. An antibody specific for HSP-90 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyHSP-90 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for HSP-90 is added to the wells. After washing, Streptavidin conj µgated 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 HSP-90 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview :
Stability : The stability of ELISA 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. The loss rate was determined by accelerated thermal degradation test. Keep the kit at 37°C for 4 and 7 days, and compare O.D.values of the kit kept at 37°C with that of at recommended temperature. (referring from China Biological Products Standard, which was calc µLated by the Arrhenius equation. For ELISA kit, 4 days storage at 37°C can be considered as 6 months at 2 - 8°C, which means 7 days at 37°C equaling 12 months at 2 - 8°C).