MMADHC 抗体
(Methylmalonic Aciduria (Cobalamin Deficiency) CblD Type, with Homocystinuria (MMADHC))
This gene encodes a mitochondrial protein that is involved in an early step of vitamin B12 metabolism. Vitamin B12 (cobalamin) is essential for normal development and survival in humans. Mutations in this gene cause methylmalonic aciduria and homocystinuria type cblD (MMADHC), a disorder of cobalamin metabolism that is characterized by decreased levels of the coenzymes adenosylcobalamin and methylcobalamin. Pseudogenes have been identified on chromosomes 11 and X.[provided by RefSeq, Nov 2008].
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40 results
MMADHC
适用: 人, 小鼠, 大鼠, Cow, 犬, 山羊, 豚鼠, 马, 兔, 斑马鱼
WB
宿主: 兔
Polyclonal
unconjugated
1 image
MMADHC
适用: 人, 小鼠, 大鼠, Cow, 犬, 山羊, 豚鼠, 马, 兔, 斑马鱼
WB
宿主: 兔
Polyclonal
unconjugated
1 image
Aliases for MMADHC 抗体
methylmalonic aciduria and homocystinuria, cblD type (MMADHC) 抗体methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria (Mmadhc) 抗体
methylmalonic aciduria and homocystinuria, cblD type (Mmadhc) 抗体
2010311D03Rik 抗体
AI314967 抗体
C2orf25 抗体
cblD 抗体
CL25022 抗体
RGD1303272 抗体
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