RMND1 抗体
(Required For Meiotic Nuclear Division 1 Homolog (RMND1))
The protein encoded by this gene belongs to the evolutionary conserved sif2 family of proteins that share the DUF155 domain in common. This protein is thought to be localized in the mitochondria and involved in mitochondrial translation. Mutations in this gene are associated with combined oxidative phosphorylation deficiency-11. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2012].
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11 results
RMND1
适用: 人
ELISA, IF (cc), IF (p), IHC (fro), IHC (p)
宿主: 兔
Polyclonal
unconjugated
Latest Publications for our RMND1 抗体
: "Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutation." in: American journal of human genetics, Vol. 91, Issue 4, pp. 729-36, (2012) (PubMed).Aliases for RMND1 抗体
required for meiotic nuclear division 1 homolog (RMND1) 抗体required for meiotic nuclear division 1 homolog (rmnd1) 抗体
required for meiotic nuclear division 1 homolog (Rmnd1) 抗体
0610042C05Rik 抗体
AA408137 抗体
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bA351K16 抗体
bA351K16.3 抗体
C6orf96 抗体
COXPD11 抗体
DKFZp469I1433 抗体
Iag-1 抗体
RGD1309546 抗体
RMD1 抗体
zgc:113022 抗体
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