MMAB Polyclonal Antibody

Background:
This gene encodes a protein that catalyzes the final step in the conversion of vitamin B(12) into adenosylcobalamin (AdoCbl), a vitamin B12-containing coenzyme for methylmalonyl-CoA mutase. Mutations in the gene are the cause of vitamin B12-dependent methylmalonic aciduria linked to the cblB complementation group. Alternatively spliced transcript variants have been found.

Research Area: Metabolism, Signal transduction

Synonyms:
aquocob(I)alamin vitamin B12s adenosyltransferase, ATP:cob(I)alamin adenosyltransferase , ATP:corrinoid adenosyltransferase, ATR , c-diamide adenosyltransferase, cblB, Cob, Cob(I)alamin adenosyltransferase, Cob(I)yrinic acid a, cob(I)yrinic acid a c diamide adenosyltransferase mitochondrial, Methylmalonic aciduria (cobalamin deficiency) cblB type, Methylmalonic aciduria type B protein, MGC20496, mitochondrial, MMAB, MMAB gene, MMAB, OTTHUMP00000240563, OTTHUMP00000240564

Immunogen: Fusion protein of human MMAB

Swissprot: Q96EY8
Gene Accession: BC011831

Calculated MW: 27 kDa
Observed MW: Refer to figures

Purification Method: Antigen affinity purification

Buffer: PBS with 0.05% NaN3 and 40% Glycerol, pH7.4

Concentration: 1.02 mg/mL
Dilution: WB 1:1000-1:5000, ELISA 1:5000-1:10000

Storage:
Store at -20°C. Avoid freeze / thaw cycles.