LETM1 Rabbit Polyclonal Antibody

Ab type

Primary antibody

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.

Reactivity

Human, Mouse, Rat

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Immunogen

Synthesized peptide derived from human LETM1

Storage Stability

-20°C for 1 year

Concentration

1 mg/ml

MolecularWeight_Da

81290

synonyms

LETM1