LETM1 Antilichaam

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.

3954

O95202

Human, Mouse, Rat

Recombinant fusion protein containing a sequence corresponding to amino acids 1-140 of human LETM1 (NP_036450.1) .

Unconjugated

Primary Antibodies

Other

Affinity purification

A-431

Batch dependent

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

None

Blue Ice

Store at -20˚ C. Avoid freeze / thaw cycles.

Observed: 83kDa

IgG

WB: 1:500 - 1:2000

LETM1

HeLa

Mouse heart

Mouse liver

Rat brain

Leucine zipper-EF-hand containing transmembrane protein 1

Homo sapiens

LETM1

WB

Liquid