GPR143 Antilichaam

This gene encodes a protein that binds to heterotrimeric G proteins and is targeted to melanosomes in pigment cells. This protein is thought to be involved in intracellular signal transduction mechanisms. Mutations in this gene cause ocular albinism type 1, also referred to as Nettleship-Falls type ocular albinism, a severe visual disorder. A related pseudogene has been identified on chromosome Y.

4935

P51810

Human, Mouse, Rat

Recombinant fusion protein containing a sequence corresponding to amino acids 314-404 of human GPR143 (NP_000264.2) .

Unconjugated

Primary Antibodies

Neuroscience, Signal Transduction

Affinity purification

U-251MG

Batch dependent

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

None

Blue Ice

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

Observed: 44kDa

IgG

WB: 1:1000 - 1:2000

GPR143

BT-474

SW480

Mouse liver

Mouse kidney

Rat kidney

G protein-coupled receptor 143

Homo sapiens

NYS6, OA1, G-protein coupled receptor 143, ocular albinism 1, ocular albinism type 1 protein

WB

Liquid