MMAA 抗体
(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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31 results
MMAA
适用: 人, 小鼠
WB, IHC (p)
宿主: 兔
Polyclonal
RB24782
unconjugated
Aliases for MMAA 抗体
methylmalonic aciduria (cobalamin deficiency) type A (Mmaa) 抗体methylmalonic aciduria (cobalamin deficiency) cblA type (MMAA) 抗体
methylmalonic aciduria (cobalamin deficiency) cblA type (Mmaa) 抗体
2810018E08Rik 抗体
AI840684 抗体
cblA 抗体
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