ABCbiolab
SKU:ABCC25007
ELISA Kit for S-Adenosyl Methionine (SAM)
ELISA Kit for S-Adenosyl Methionine (SAM)
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Format
48T, 96T, 96T×5, 96T×10, 96T×100
Detection range
12.35-1,000ng/mL
Application
Enzyme-linked immunosorbent assay for Antigen Detection.
Organism species
Pan-species (General)
Sensitivity
The minimum detectable dose of this kit is typically less than 4.84ng/mL
Sample type
serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
Assay length
2h
Method
Competitive Inhibition
Test principle
This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to S-Adenosyl Methionine (SAM) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled S-Adenosyl Methionine (SAM) and unlabeled S-Adenosyl Methionine (SAM) (Standards or samples) with the pre-coated antibody specific to S-Adenosyl Methionine (SAM). After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of S-Adenosyl Methionine (SAM) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of S-Adenosyl Methionine (SAM) in the sample.
Alternative Names
SAMe; SAM-e; S-Adenosylmethionine; S-(5'-Adenosyl)-L-Methionine Chloride
Item Name
S-Adenosyl Methionine
Research Area
Reference
Hyperhomocysteinemia causes ER stress and impaired autophagy that is reversed by Vitamin B supplementation;Attenuated expression of MTR in both prenatally androgenized mice and women with the hyperandrogenic phenotype of PCOS;Metabolic engineering of Acremonium chrysogenum for improving cephalosporin C production independent of methionine stimulation;
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