Search
Search
Abnova
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.promotions']}}
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.viewpromo']}}
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.promocode']}}: {{promo.promoCode}} {{promo.promoTitle}} {{promo.promoDescription}}. {{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.learnmore']}}
Product may be used with Western Blot (Cell lysate).
Immunogen sequence: AFREERKMVQ EDEKIGFEIS ENQKRQAAMT VRKVPKQKGV NSARSVPPSY PPPQDPLNHG QYLVPDGIAQ SQVFEFTEPK RSQSPFWQNF SRLTPFKK
The protein encoded by this gene is a Rho-like GTPase that switches between the active state and inactive state to regulate CDC42 and other genes. Defects in this gene are a cause of startle disease with epilepsy, also known as hyperekplexia with epilepsy. Three transcript variants encoding different isoforms have been found for this gene.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: Cdc42 guanine nucleotide exchange factor (GEF) 9; Collybistin; hPEM-2 collybistin; PEM-2 homolog; Rac/Cdc42 guanine nucleotide exchange factor 9; Rho guanine nucleotide exchange factor 9
基因别名: ARHDH9; ARHGEF9; COLLYBISTIN; EIEE8; HPEM-2; KIAA0424; PEM-2; PEM2
UniProt ID: (Human) O43307
Entrez Gene ID: (Human) 23229