LETM1 antibody (clone 6F7), anti-human

Background:
This gene encodes a protein that is localized to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19.

Other Names:
LETM1 and EF-hand domain-containing protein 1, mitochondrial, Leucine zipper-EF-hand-containing transmembrane protein 1, LETM1

Antigen Type:
Recombinant Protein

Gene Name: LETM1 (HGNC:6556)
Gene ID: 3954
NCBI Accession: NP_036450.1
Primary Accession: O95202
Other Accession: NM_012318
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .