ARHGEF9 polyclonal, anti-human, mouse, rat

Background:
The protein encoded by this gene is a Rho-like GTPase that switches between the active (GTP-bound) state and inactive (GDP-bound) state to regulate CDC42 and other genes. Defects in this gene are a cause of startle disease with epilepsy (STHEE), also known as hyperekplexia with epilepsy. Three transcript variants encoding different isoforms have been found for this gene.

Synonyms: PEM2, EIEE8, PEM-2, HPEM-2, COLLYBISTIN

Cellular Location: Cytoplasm

Immunogen:
Recombinant protein of human ARHGEF9

Gene Symbol: ARHGEF9

Gene ID: 23229

Swiss prot: O43307

Calculated MW: 61kDa

Recommended dilution:
WB 1:1000-5000, IHC 1:50-200,

Purity:
Affinity purification

Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.

Storage:
Store at -20℃. Avoid freeze / thaw cycles.