MMAB Proteins
(Methylmalonic Aciduria (Cobalamin Deficiency) CblB Type (MMAB))
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. [provided by RefSeq, Apr 2011].
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5 results
MMAB
Origin: Human
Host: Wheat germ
Recombinant
ELISA, AP, AA, WB
1 image
MMAB
Origin: Human
Host: Escherichia coli (E. coli)
Recombinant
> 95 % by SDS - PAGE
SDS
1 image
MMAB
Origin: Human
Host: HEK-293 Cells
Recombinant
> 80 % as determined by SDS-PAGE and Coomassie blue staining
AbP, STD
1 image
Aliases for MMAB Proteins
methylmalonic aciduria (cobalamin deficiency) cblB type (MMAB) Proteinsmethylmalonic aciduria (cobalamin deficiency) cblB type homolog (human) (Mmab) Proteins
9130222L19Rik Proteins
ATR Proteins
cblB Proteins
cob Proteins
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