SLC25A20 Antilichaam

This gene product is one of several closely related mitochondrial-membrane carrier proteins that shuttle substrates between cytosol and the intramitochondrial matrix space. This protein mediates the transport of acylcarnitines into mitochondrial matrix for their oxidation by the mitochondrial fatty acid-oxidation pathway. Mutations in this gene are associated with carnitine-acylcarnitine translocase deficiency, which can cause a variety of pathological conditions such as hypoglycemia, cardiac arrest, hepatomegaly, hepatic dysfunction and muscle weakness, and is usually lethal in new born and infants.

788

O43772

Human, Mouse, Rat

Recombinant fusion protein containing a sequence corresponding to amino acids 1-301 of human SLC25A20 (NP_000378.1) .

Unconjugated

Primary Antibodies

Other

Affinity purification

Mouse liver

Batch dependent

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

None

Blue Ice

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

Observed: 39kDa

IgG

WB: 1:500 - 1:2000

SLC25A20

Solute carrier family 25 (carnitine/acylcarnitine translocase), member 20

Homo sapiens

SLC25A20, CAC, CACT

WB

Liquid