LETM1 Antibody (C-term) Blocking Peptide
€363.00
In stock
SKU
AC-BP17447b
Background:
This gene encodes a protein that is localized to the innermitochondrial membrane. The protein functions to maintain themitochondrial tubular shapes and is required for normalmitochondrial morphology and cellular viability. Mutations in thisgene cause Wolf-Hirschhorn syndrome, a complex malformationsyndrome caused by the deletion of parts of the distal short arm ofchromosome 4. Related pseudogenes have been identified onchromosomes 8, 15 and 19.
Other Names:
LETM1 and EF-hand domain-containing protein 1, mitochondrial, Leucine zipper-EF-hand-containing transmembrane protein 1, LETM1
Gene Name: LETM1 (HGNC:6556)
Gene ID: 3954
Primary Accession: O95202
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
This gene encodes a protein that is localized to the innermitochondrial membrane. The protein functions to maintain themitochondrial tubular shapes and is required for normalmitochondrial morphology and cellular viability. Mutations in thisgene cause Wolf-Hirschhorn syndrome, a complex malformationsyndrome caused by the deletion of parts of the distal short arm ofchromosome 4. Related pseudogenes have been identified onchromosomes 8, 15 and 19.
Other Names:
LETM1 and EF-hand domain-containing protein 1, mitochondrial, Leucine zipper-EF-hand-containing transmembrane protein 1, LETM1
Gene Name: LETM1 (HGNC:6556)
Gene ID: 3954
Primary Accession: O95202
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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