MMAA Proteins
(Methylmalonic Aciduria (Cobalamin Deficiency) Type A (MMAA))
The protein encoded by this gene is involved in the translocation of cobalamin into the mitochondrion, where it is used in the final steps of adenosylcobalamin synthesis. Adenosylcobalamin is a coenzyme required for the activity of methylmalonyl-CoA mutase. Defects in this gene are a cause of methylmalonic aciduria. [provided by RefSeq, Jul 2008].
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3 results
MMAA
Origin: Human
Host: Wheat germ
Recombinant
ELISA, AP, AA, WB
1 image
MMAA
Origin: Human
Host: HEK-293 Cells
Recombinant
> 80 % as determined by SDS-PAGE and Coomassie blue staining
AbP, STD
1 image
Aliases for MMAA Proteins
methylmalonic aciduria (cobalamin deficiency) type A (Mmaa) Proteinsmethylmalonic aciduria (cobalamin deficiency) cblA type (MMAA) Proteins
methylmalonic aciduria (cobalamin deficiency) cblA type (Mmaa) Proteins
2810018E08Rik Proteins
AI840684 Proteins
cblA Proteins
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