LETM1 rabbit pAb - ES15167

LETM1 rabbit pAb

Sizes: 50μL, 100μL

Catalogue Numbers: ES15167-50, ES15167-100

Citations, Manuals and MSDS Available upon request.

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. [provided by RefSeq, Oct 2009],

Source: Rabbit

Applications: WB

Dilution: WB 1: 500-2000

Reactivity: Human; Mouse; Rat

Immunogen: Synthesized peptide derived from human LETM1 AA range: 574-624

Storage and Stability: -20°C/1 year

Clonality: Polyclonal

Isotype: IgG

Concentration: 1 mg/ml

Human Gene ID: 3954

Human SWISS Prot NO: O95202

Subcellular Location: Mitochondrion inner membrane; Single-pass membrane protein.

Research Use Only