Porcine SUCLG2 ELISA KIT

Packing  96Tests

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

Gene Name  SUCLG2

Protein Name  Succinate--CoA ligase [GDP-forming] subunit beta, mitochondrial

Alternative Name

Porcine SUCLG2 ELISA KIT, Porcine G-SCS ELISA KIT ,Porcine GBETA ELISA KIT ,Porcine GTPSCS ELISA KIT ,Porcine succinate--CoA ligase [GDP-forming] subunit beta mitochondrial ELISA KIT ,Porcine GTP-specific succinyl-CoA synthetase beta subunit ELISA KIT ,Porcine GTP-specific succinyl-CoA synthetase subunit beta ELISA KIT ,Porcine SCS-betaG ELISA KIT ,Porcine succinyl-CoA ligase [GDP-forming] subunit beta mitochondrial ELISA KIT ,Porcine succinyl-CoA ligase GDP-forming beta chain mitochondrial ELISA KIT ,Porcine succinyl-CoA synthetase beta-G chain ELISA KIT ,Porcine succinate-CoA ligase GDP-forming beta subunit ELISA KIT

Intended use

Porcine SUCLG2 ELISA KIT allows for the in vitro quantitative determination of SUCLG2 concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.

Test principle      

The microtiter plate provided in Porcine SUCLG2 ELISA KIT has been pre-coated with an SUCLG2 antibody specific to SUCLG2. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for SUCLG2 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 SUCLG2, 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 SUCLG2 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