Brand Name: | Feiyue |
---|---|
Type: | Blood Testing Equipments |
Display type: | Standard |
Specimen: | serum plasma |
Accuracy: | sensitivity |
Model Number: | FY-EH3738 |
Place of Origin: | China (Mainland) |
Size: | 48T |
Quick Details
Specifications
Product Name |
Human EFNA1(Ephrin-A1) ELISA Kit |
Catalog NO. |
FY-EU3738 |
Alias |
EFNA1 ELISA Kit, Ephrin A1 ELISA Kit, EFNA1 ELISA Kit, TNF alpha induced protein 4 ELISA Kit, LERK1 ELISA Kit, EFL1 ELISA Kit, B61 ELISA Kit, ECKLG ELISA Kit, EPLG1 ELISA Kit, TNFAIP4 ELISA Kit, Tumor necrosis factor alpha-induced protein 4 ELISA Kit, TNF alpha-induced protein 4 ELISA Kit, EPH-related receptor tyrosine kinase ligand 1 ELISA Kit, LERK-1 ELISA Kit, Immediate early response protein B61 ELISA Kit |
Application |
EFNA1 ELISA Kit allows for the in vitro quantitative determination of EFNA1 concentrations in serum, plasma, tissue homogenates and other biological fluids |
Size |
48T, 96T |
Storage |
2-8 ℃ for 6 months |
Sensitivity |
< 0.094ng/ml |
Species |
Human |
UniProt ID |
P20827 |
CV(%) |
Intra-Assay: CV<8% |
Note |
for Research Use Only |
Human EFNA1(Ephrin-A1) Introduction
EFNA1 is a protein that in humans is encoded by the EFNA1 gene.Long term ET-1 exposure has been associated with hypertrophic cardiomyopathy.Endothelin-1 receptor antagonists (Bosentan) are used in the treatment of pulmonary hypertension. Inhibition of these receptors prevents pulmonary vasculature constriction and thus decreases pulmonary vascular resistance.
Human EFNA1(Ephrin-A1) ELISA Kit Test Methodthis kit uses sandwich ELISA to detect the concentration of Human EFNA1.
Human EFNA1-specific monoclonal antibody has been pre-coated in the wells of the supplied microplate.Standards samples and controls are added to interact with the immobilized antibody. A sandwich complex is formed by additional anti-human EFNA1 antibody with HRP-Streptavidin.TMB solution is added to react with the sandwich forming optical signal measured by microplate reader.the concentration of human EFNA1 in the sample can be calculated by comparing the absorbance of the sample with the standard curve.