Rat Nicotinamide riboside kinase 1, NRK1 ELISA KIT

96 Tests

Operating instruction

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

Synonyms

Search name

NRK1,C9orf95,Nicotinamide riboside kinase 1,NRK 1,NmR-K 1,Ribosylnicotinic acid kinase 1;2.7.1.173;Nicotinic acid riboside kinase 1);Ribosylnicotinamide kinase 1,RNK 1, NMRK1,bA235O14.2; NRK 1; RNK 1; nicotinic acid riboside kinase 1; nmR-K 1; ribosylnicotinamide kinase 1; ribosylnicotinic acid kinase 1; nicotinamide riboside kinase 1

Search name

Rat NRK1 ELISA KIT ,Rat C9orf95 ELISA KIT ,Rat Nicotinamide riboside kinase 1 ELISA KIT ,Rat NRK 1 ELISA KIT ,Rat NmR-K 1 ELISA KIT ,Rat Ribosylnicotinic acid kinase ELISA KIT, Rat Nicotinic acid riboside kinase 1 ELISA KIT, Rat Ribosylnicotinamide kinase 1 ELISA KIT ,Rat RNK 1 ELISA KIT ,Rat NMRK1 ELISA KIT ,Rat bA235O14.2 ELISA KIT ,Rat NRK 1 ELISA KIT ,Rat RNK 1 ELISA KIT ,Rat nicotinic acid riboside kinase 1 ELISA KIT ,Rat nmR-K 1 ELISA KIT ,Rat ribosylnicotinamide kinase 1 ELISA KIT ,Rat ribosylnicotinic acid kinase 1 ELISA KIT ,Rat nicotinamide riboside kinase 1 ELISA KIT

Intended use

This immunoassay kit allows for the in vitro quantitative determination of Rat Nicotinamide riboside kinase 1, NRK1 concentrations in serum, Plasma, tissue homogenates and Cell culture supernates and Other biological fluids.

Test principle

The microtiter plate provided in this kit has been pre-coated with an antibody specific to *. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated polyclonal antibody preparation specific for * and Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. Only those wells that contain *, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 * in the samples is then determined by comparing the O.D. of the samples to the standard curve.