Mouse ACACa(Acetyl Coenzyme A Carboxylase Alpha) ELISA Kit

3h

20ng/mL

Sandwich

0.117ng/mL

Mus musculus

0.312-20ng/mL

Metabolic pathway;

ACAC; ACC1; ACCA; ACAC; ACC2; ACCB; ACACB; ACACA; Acetyl CoA Carboxylase; Biotin carboxylase

E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays,E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays

N terminal acetylation or CH3CO as epigenetic regulation of Mouse ACACa( Coenzyme A Carboxylase Alpha) ELISA Kit by NATs.The Mouse ACACa( Coenzyme A Carboxylase Alpha) ELISA Kit is a α- or alpha protein sometimes glycoprotein present in blood.

ELISA Enzyme-linked immunosorbent assays Code 90320007 SNOMED,Mouse or mice from the Mus musculus species are used for production of mouse monoclonal antibodies or mabs and as research model for humans in your lab. Mouse are mature after 40 days for females and 55 days for males. The female mice are pregnant only 20 days and can give birth to 10 litters of 6-8 mice a year. Transgenic, knock-out, congenic and inbread strains are known for C57BL/6, A/J, BALB/c, SCID while the CD-1 is outbred as strain.

The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Acetyl Coenzyme A Carboxylase Alpha (ACACα). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Acetyl Coenzyme A Carboxylase Alpha (ACACα). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Acetyl Coenzyme A Carboxylase Alpha (ACACα), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Acetyl Coenzyme A Carboxylase Alpha (ACACα) in the samples is then determined by comparing the O.D. of the samples to the standard curve.