epitope mapping within an internal region of TBC1D2B of human origin
Modification Notes
GTPase-activating proteins (GAPs) accelerate the intrinsic rate of GTP hydrolysis of Ras-related proteins, resulting in downregulation of their active form. TBC1D2B (TBC1 domain family, member 2B) is a 963 amino acid protein that is thought to play a role in GTPase activation. Containing one PH domain and a Rab-GAP TBC domain, TBC1D2B exists as three alternatively spliced isoforms. The gene encoding TBC1D2B maps to human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of TBC1D2B of mouse, rat and human origin by WB, IP, IF and ELISA non cross-reactive with other TBC1D family members also reactive with additional species, including equine, canine, bovine, porcine and avian:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope mapping within an internal region of TBC1D2B of human origin
Tissue Specificity
epitope mapping within an internal region of TBC1D2B of human origin
Western blot analysis of TBC1D2B expression in non-transfected: (A) and human TBC1D2B transfected: (B) 293T whole cell lysates.
Application Notes
recommended for detection of TBC1D2B of mouse, rat and human origin by WB, IP, IF and ELISA non cross-reactive with other TBC1D family members also reactive with additional species, including equine, canine, bovine, porcine and avian:
Additional Information
Form
Liquid
Storage Instructions
For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.