Human USP39 ELISA KIT

Packing  96Tests

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

Gene Name  USP39

Protein Name  U4/U6.U5 tri- snRNP- associated protein 2

Alternative Name

Human USP39 ELISA KIT ,Human 65K ELISA KIT ,Human CGI-21 ELISA KIT ,Human HSPC332 ELISA KIT ,Human SAD1 ELISA KIT ,Human SNRNP65 ELISA KIT ,Human U4/U6.U5 tri-snRNP-associated protein 2 ELISA KIT ,Human SAD1 homolog ELISA KIT ,Human SnRNP assembly defective 1 homolog ELISA KIT ,Human U4/U6.U5 tri-snRNP-associated 65 kDa protein ELISA KIT ,Human inactive ubiquitin-specific peptidase 39 ELISA KIT ,Human small nuclear ribonucleoprotein 65kDa (U4/U6.U5) ELISA KIT ,Human ubiquitin specific protease 39 ELISA KIT ,Human ubiquitin specific peptidase 39 ELISA KIT

Human USP39 ELISA KIT Range  0.156-10ng/mL

Intended use

Human USP39 ELISA KIT allows for the in vitro quantitative determination of USP39 concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.

Test principle      

The microtiter plate provided in Human USP39 ELISA KIT has been pre-coated with an USP39 antibody specific to USP39. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for USP39 and then 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 USP39, 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 USP39 in the samples is then determined by comparing the O.D. of the samples to the standard curve.

Sample collection and storage 

Serum - Use a serum separator tube (SST) and allow samples to clot for 30 minutes before centrifugation for 15 minutes at approximately 1000 × g. Remove serum and assay immediately or aliquot and store samples at -20