Human eosinophil-derived neurotoxin ELISA Kit;Human RNase UpI-2 ELISA Kit;Human ribonuclease 2 ELISA Kit;Human RNase 2 ELISA Kit;Human ribonuclease US ELISA Kit;Human EDN ELISA Kit;Human RNS2 ELISA Kit;Human RAF3 ELISA Kit;Human ribonuclease A family member 2 ELISA Kit;Human non-secretory ribonuclease ELISA Kit;Human ribonuclease A F3 ELISA Kit;Human ribonuclease, RNase A family, 2 (liver, eosinophil-derived neurotoxin) ELISA Kit;
Catalog
E026718
species
Human
GeneRNASE2
SpecificityThis assay has high sensitivity and excellent specificity for detection of RNASE2. No significant cross-reactivity or interference between RNASE2 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between RNASE2 and all the analogues, therefore, cross reaction may still exist in some cases.
Intended UseHuman RNASE2 ELISA Kit allows for the in vitro quantitative determination of RNASE2 , concentrations in serum, Plasma , tissue homogenates and Cell culture supernates and Other biological fluids.
StorageStore the whole ELISA kit at 4℃
Product Categories/FamilyEpigenetics and Nuclear Signaling
Product Description specificalIntended Uses: This RNASE2 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human RNASE2. This ELISA kit for research use only, not for therapeutic or diagnostic applications!
Principle of the Assay||RNASE2 ELISA kit applies the competitive enzyme immunoassay technique utilizing a Polyclonal anti-RNASE2 antibody and an RNASE2-HRP conjugate. The assay sample and buffer are incubated together with RNASE2-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 RNASE2 concentration since RNASE2 from samples and RNASE2-HRP conjugate compete for the anti-RNASE2 antibody binding site. Since the number of sites is limited, as more sites are occupied by RNASE2 from the sample, fewer sites are left to bind RNASE2-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The RNASE2 concentration in each sample is interpolated from this standard curve.
Human Non-secretory ribonuclease Protein information