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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10 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
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