Human ARHGEF9 protein
Recombinant protein from the full-length sequence of Homo sapiens Cdc42 guanine nucleotide exchange factor 9 (ARHGEF9), transcript variant 1 (NM_015185), with a His tag.
COLLYBISTIN; EIEE8; HPEM-2; PEM-2; PEM2
>90% by SDS-PAGE gel and Coomassie Blue staining
Antigens, Western, ELISA and other in vitro binding or in vivo functional assays, and protein-protein interaction studies; For research & development use only!
Purified protein formulated in a sterile solution of PBS buffer, pH7.2, without any preservatives
Endotoxin level is < 0.1 ng/µg of protein (<1EU /µg)
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.[provided by RefSeq, Mar 2010].
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