H/ACA ribonucleoprotein comple

Mouse H/ACA ribonucleoprotein complex subunit 1, GAR1 ELISA KIT

96 Tests

Operating instructions

FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS!PLEASE READ THROUGH ENTIRE PROCEDURE BEFORE BEGINNING!

Synonyms

GAR1,GAR1 ribonucleoprotein; snoRNP protein GAR1; GAR1 ribonucleoprotein homolog; NOLA1; nucleolar protein family A member 1; nucleolar protein family A member 1,H/ACA small nucleolar RNPs, H/ACA ribonucleoprotein complex subunit 1,Nucleolar protein family A member 1,snoRNP protein GAR1,

Search name

Mouse GAR1 ELISA KIT ,Mouse GAR1 ribonucleoprotein ELISA KIT ,Mouse snoRNP protein GAR1 ELISA KIT ,Mouse GAR1 ribonucleoprotein homolog ELISA KIT ,Mouse NOLA1 ELISA KIT ,Mouse nucleolar protein family A member 1 ELISA KIT ,Mouse nucleolar protein family A member 1 ELISA KIT ,Mouse H/ACA small nucleolar RNPs ELISA KIT ,Mouse  H/ACA ribonucleoprotein complex subunit 1 ELISA KIT ,Mouse Nucleolar protein family A member 1 ELISA KIT ,Mouse snoRNP protein GAR1 ELISA KIT

Intended use

This immunoassay kit allows for the in vitro quantitative determination of Mouse H/ACA ribonucleoprotein complex subunit 1concentrations in serum, plasma, tissue homogenates, cell culture supernates, and other biological fluids.

Test principle

The ELISA is based on the competitive binding enzyme immunoassaytechnique. The microtiter plate provided in this kit has been pre-coated with an antibody specific toH/ACA ribonucleoprotein complex subunit 1, During the reaction,H/ACA ribonucleoprotein complex subunit 1in the sample or standard competes with a fixed amount of biotin-labeledH/ACA ribonucleoprotein complex subunit 1 for sites on a pre-coated Monoclonal antibody specific to H/ACA ribonucleoprotein complex subunit 1. Excess conjugate and unbound sample or standard are washed from the plate. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Thena TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of H/ACA ribonucleoprotein complex subunit 1 in the samples is then determined by comparing the O.D. of the samples to the standard curve.

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