Anti-Human/Mouse/Rat ARHGEF9 Polyclonal Antibody

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.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA12917
Size 100μl
Host Type Rabbit
Immunogen Recombinant protein of human ARHGEF9
Specificity Detected in brain. Detected at low levels in heart.
Isotype IgG
Reacitivity Human,Mouse,Rat
Clone
Uniprot O43307
Concentration 0.4 mg/mL
Dilution WB 1:1000-1:5000, IHC 1:50-1:200
Formulation
Application WB,IHC,ELISA
Other Names 9630036L12Rik,A230067K14,ARHG9,Arhgef9,Cdc42 guanine nucleotide exchange factor (GEF) 9,Collybistin,collybistin I,EIEE8,HPEM 2,hPEM-2 collybistin,KIAA0424,mKIAA0424,OTTHUMP00000023424,OTTHUMP00000023425,OTTHUMP00000023427,PEM 2,PEM 2 homolog,PEM-2 homolog,PEM2,Rac/Cdc42 guanine nucleotide exchange factor 9,Rho guanine nucleotide exchange factor 9,RP11 357C3.4,RP23 230K20.3
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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