Elisa 96 Wells

Volume : 96 Test. Other Volumes are also available. Please Inquire.
Species Reactivity : Human (Homo sapiens)
UniProt : N/A
Abbreviation : 8-iso-PGF2a
Alternative Names : N/A
Application : ELISA
Range : 31.25-2000 pg/mL
Sensitivity : 15 pg/mL
Intra-AssayCV : ≤3.8%
Inter-AssayCV : ≤8.6%
Recovery : 0,98
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 8-iso-PGF2a in samples. An antibody specific for 8-iso-PGF2a has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any8-iso-PGF2a present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for 8-iso-PGF2a 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 8-iso-PGF2a bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : The isoprostanes are a family of eicosanoids of non-enzymatic origin produced by the random oxidation of tissue phospholipids by oxygen radicals. Isoprostanes appear as artifacts in tissue and plasma samples which have undergone oxidative degradation during prolonged or improper storage. They also appear in the plasma and urine under normal conditions and are elevated by oxidative stress. At least one of the isoprostanes, 8-isoprostane (8-epi PGF2α), has been shown to have biological activity. It is a potent p µLmonary and renal vasoconstrictor1 and has been implicated as a causative mediator of hepatorenal syndrome and p µLmonary oxygen toxicity.2 8-Isoprostane has been proposed as a marker of antioxidant deficiency and oxidative stress and elevated levels have been found in heavy smokers.3 8-Isoprostane levels are also a relative indicator of sample integrity for lipid-containing samples such as serum, plasma, and whole cell preparations.
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 : Human (Homo sapiens)
UniProt : N/A
Abbreviation : 8-iso-PGF2a
Alternative Names : N/A
Application : ELISA
Range : 31.25-2000 pg/mL
Sensitivity : 15 pg/mL
Intra-AssayCV : ?3.8%
Inter-AssayCV : ?8.6%
Recovery : 0.98
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 8-iso-PGF2a in samples. An antibody specific for 8-iso-PGF2a has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any8-iso-PGF2a present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for 8-iso-PGF2a 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 8-iso-PGF2a bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : The isoprostanes are a family of eicosanoids of non-enzymatic origin produced by the random oxidation of tissue phospholipids by oxygen radicals. Isoprostanes appear as artifacts in tissue and plasma samples which have undergone oxidative degradation during prolonged or improper storage. They also appear in the plasma and urine under normal conditions and are elevated by oxidative stress. At least one of the isoprostanes, 8-isoprostane (8-epi PGF2?), has been shown to have biological activity. It is a potent p µLmonary and renal vasoconstrictor1 and has been implicated as a causative mediator of hepatorenal syndrome and p µLmonary oxygen toxicity.2 8-Isoprostane has been proposed as a marker of antioxidant deficiency and oxidative stress and elevated levels have been found in heavy smokers.3 8-Isoprostane levels are also a relative indicator of sample integrity for lipid-containing samples such as serum, plasma, and whole cell preparations.
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 : Cell Biology
Uniprot ID :
Species : Human
Former Code :
Alias :
Product Type : ELISA Kit
Sample Type : serum, urine, tissue homogenates
Detect Range : 2 ng/ml-800 ng/ml
Sensitivity : 0.8 ng/ml
Antigen Name : 8-Hydroxydeoxyguanosine (8-OHdG)
Abbreviation : 8-OHdG
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 : Human (Homo sapiens)
UniProt : N/A
Abbreviation : 8-OHdG
Alternative Names : N/A
Application : ELISA
Range : 12.5-800 ng/mL
Sensitivity : 6.0 ng/mL
Intra-AssayCV : ?3.9%
Inter-AssayCV : ?7.5%
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 8-OHdG in samples. An antibody specific for 8-OHdG has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any8-OHdG present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for 8-OHdG 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 8-OHdG bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : 8-oxo-7,8-dihydro-2 deoxyguanosine(8-OHdG), is probably the most important product of "oxidative stress” in DNA. Its concentration in DNA is, in fact. a quantitative analysis of the degree of DNA damage that an organism has undergone. Due to the importance of 8-OHdG of nucleic acidg in mutagenesis, carcinogenesis and aging, numerous chemical and biological investigations have been made on this subject in the past time. Kuchino and co-workers have found that 8-OHdG residue in DNA is misreading during the process of DNA replication. Recently, some reports have been presented on high 8-OHdG levels in patients suffering from various diseases such as chronic hepatitis, Fanconi s anemia, diabetes mellitus and Helicobacter pylori infections. As a res µLt, 8-OHdG is a usef µL marker for the study of DNA damage arising from reactive oxygen species and is of great significance for cancer research.
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 : Others
Uniprot ID :
Species : Human
Former Code :
Alias :
Product Type : ELISA Kit
Sample Type : serum, urine, tissue homogenates
Detect Range : 78 pg/ml-5000 pg/ml
Sensitivity : 19.5 pg/ml
Antigen Name : 8-epi-prostaglandin F2alpha,8-epi-PGF2α
Abbreviation : 8-epi-PGF2α
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

Volume : 96 Test. Other Volumes are also available. Please Inquire.
Species Reactivity : Human (Homo sapiens)
UniProt : N/A
Abbreviation : 8-epi-PGF2a
Alternative Names : N/A
Application : ELISA
Range : 24.69-2000 pg/mL
Sensitivity : 9.55 pg/mL
Intra-AssayCV : ≤5.5%
Inter-AssayCV : ≤10.7%
Recovery : 103
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 8-epi-PGF2a in samples. An antibody specific for 8-epi-PGF2a has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any8-epi-PGF2a present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for 8-epi-PGF2a 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 8-epi-PGF2a bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : The isoprostanes are a family of eicosanoids of non-enzymatic origin produced by the random oxidation of tissue phospholipids by oxygen radicals. Isoprostanes appear as artifacts in tissue and plasma samples which have undergone oxidative degradation during prolonged or improper storage. They also appear in the plasma and urine under normal conditions and are elevated by oxidative stress. At least one of the isoprostanes, 8-isoprostane (8-epi PGF2α), has been shown to have biological activity. It is a potent p µLmonary and renal vasoconstrictor1 and has been implicated as a causative mediator of hepatorenal syndrome and p µLmonary oxygen toxicity.2 8-Isoprostane has been proposed as a marker of antioxidant deficiency and oxidative stress and elevated levels have been found in heavy smokers.3 8-Isoprostane levels are also a relative indicator of sample integrity for lipid-containing samples such as serum, plasma, and whole cell preparations.
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 : Human (Homo sapiens)
UniProt : N/A
Abbreviation : 8-epi-PGF2a
Alternative Names : N/A
Application : ELISA
Range : 24.69-2000 pg/mL
Sensitivity : 9.55 pg/mL
Intra-AssayCV : ?5.5%
Inter-AssayCV : ?10.7%
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 8-epi-PGF2a in samples. An antibody specific for 8-epi-PGF2a has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any8-epi-PGF2a present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for 8-epi-PGF2a 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 8-epi-PGF2a bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : The isoprostanes are a family of eicosanoids of non-enzymatic origin produced by the random oxidation of tissue phospholipids by oxygen radicals. Isoprostanes appear as artifacts in tissue and plasma samples which have undergone oxidative degradation during prolonged or improper storage. They also appear in the plasma and urine under normal conditions and are elevated by oxidative stress. At least one of the isoprostanes, 8-isoprostane (8-epi PGF2?), has been shown to have biological activity. It is a potent p µLmonary and renal vasoconstrictor1 and has been implicated as a causative mediator of hepatorenal syndrome and p µLmonary oxygen toxicity.2 8-Isoprostane has been proposed as a marker of antioxidant deficiency and oxidative stress and elevated levels have been found in heavy smokers.3 8-Isoprostane levels are also a relative indicator of sample integrity for lipid-containing samples such as serum, plasma, and whole cell preparations.
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 : Human (Homo sapiens)
UniProt : Q7L2J0
Abbreviation : MEPCE
Alternative Names : BCDIN3; FLJ20257; 7SK snRNA methylphosphate capping enzyme|bin3; bicoid-interacting 3; homolog
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?3.6%
Inter-AssayCV : ?7.6%
Recovery : 1
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 MEPCE in samples. An antibody specific for MEPCE has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyMEPCE present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for MEPCE 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 MEPCE 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 : Q9UBM7
Species : Human
Former Code :
Alias : SLOS, delta-7-dehydrocholesterol reductase|sterol delta-7-reductase
Product Type : ELISA Kit
Sample Type : serum, plasma, tissue homogenates
Detect Range : 31.25 pg/ml-2000 pg/ml
Sensitivity : 7.8 pg/ml
Antigen Name : 7-dehydrocholesterol reductase
Abbreviation : DHCR7
Protein Biological Process 1 : Biosynthesis/Metabolism
Protein Biological Process 2 : Lipogenesis and lipometabolism
Protein Biological Process 3 : Cholesterol biosynthesis
Assay Time : 1-5h
Sample Volume : 50-100 µL
Detection Wavelength : 450 nm
Delievery Date : 5-7 working days

Species Reactivity : Human (Homo sapiens)
UniProt : Q9UBM7
Abbreviation : DHCR7
Alternative Names : SLOS; delta-7-dehydrocholesterol reductase|sterol delta-7-reductase
Application : ELISA
Range : 0.156-10 ng/mL
Sensitivity : 0.055 ng/mL
Intra-AssayCV : ?6.2%
Inter-AssayCV : ?10.5%
Recovery : 0.99
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 DHCR7 in samples. An antibody specific for DHCR7 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyDHCR7 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for DHCR7 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 DHCR7 bound in the initial step. The color development is stopped and the intensity of the color is measured.
Product Overview : 7-dehydrocholesterol reductasean enzyme that removes the C(7-8) double bond in the B ring of sterols and catalyzes the conversion of 7-dehydrocholesterol to cholesterol. This gene is ubiquitously expressed and its transmembrane protein localizes to the endoplasmic retic µLum membrane and nuclear outer membrane. Mutations in this gene cause Smith-Lemli-Opitz syndrome (SLOS); a syndrome that is metabolically characterized by reduced serum cholesterol levels and elevated serum 7-dehydrocholesterol levels and phenotypically characterized by mental retardation, facial dysmorphism, syndactyly of second and third toes, and holoprosencephaly in severe cases to minimal physical abnormalities and near-normal intelligence in mild cases. Alternative splicing res µLts in m µLtiple transcript variants that encode the same protein.
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 : Human (Homo sapiens)
UniProt : Q9UNU6
Abbreviation : CYP8B1
Alternative Names : CP8B; CYP12; FLJ17826; 7 alpha-hydroxy-4-cholesten-3-one 12-alpha-hydroxylase|cytochrome P450; subfamily VIIIB (sterol 12-alpha-hydroxylase); polypeptide 1|sterol 12-alpha-hydroxylase
Application : ELISA
Range : Request Information
Sensitivity : Request Information
Intra-AssayCV : ?7.9%
Inter-AssayCV : ?9.2%
Recovery : 1.01
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 CYP8B1 in samples. An antibody specific for CYP8B1 has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and anyCYP8B1 present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conj µgated antibody specific for CYP8B1 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 CYP8B1 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).