OSTM1 Antilichaam

This gene encodes a protein that may be involved in the degradation of G proteins via the ubiquitin-dependent proteasome pathway. The encoded protein binds to members of subfamily A of the regulator of the G-protein signaling (RGS) family through an N-terminal leucine-rich region. This protein also has a central RING finger-like domain and E3 ubiquitin ligase activity. This protein is highly conserved from flies to humans. Defects in this gene may cause the autosomal recessive, infantile malignant form of osteopetrosis.

28962

Q86WC4

Human, Mouse, Rat

Recombinant fusion protein containing a sequence corresponding to amino acids 32-284 of human OSTM1 (NP_054747.2) .

Unconjugated

Primary Antibodies

Cancer, Cell Cycle, Signal Transduction

Affinity purification

HeLa

Batch dependent

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

None

Blue Ice

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

Observed: 30-37kDa

IgG

WB: 1:500 - 1:2000

OSTM1

293T

A-549

Raji

B cells

Mouse brain

Osteopetrosis-associated transmembrane protein 1

Homo sapiens

Osteopetrosis-associated transmembrane protein 1, Chloride channel 7 beta subunit, OSTM1, GL

WB

Liquid