GIT1 antibody

Biorbyt

GIT1 antibody

16

1 microg/ml of SMC-413 was sufficient for detection of GIT1 in 10 microg of rat brain lysate by colorimetric immunoblot analysis using Goat anti-mouse IgG:HRP as the secondary antibody.

ImmunoPrecipitation, Western Blot, ImmunoCytoChemistry

WB (1:1000) ELISA, ICC, IF, IHC, WB

Research Use Only

Monoclonal

N39B/8 (Formerly sold as S39B-8)

1 mg/ml

PerCP

Git1

GIT ArfGAP 1

ARF GAP GIT1; ARF GTPase-activating protein GIT1; CAT1; CAT-1; cool-associated and tyrosine-phosphorylated protein 1; G protein-coupled receptor kinase interacting ArfGAP 1; G protein-coupled receptor kinase-associated ADP ribosylation factor GTPase-activating protein (GIT1); G protein-coupled receptor kinase-interactor 1; GRK-interacting protein 1; GRK-interactor 1

Mouse

IgG1

ARF GTPase-activating protein GIT1

Mouse monoclonal to GIT1 (PerCP). G-protein coupled receptor (GPCR) kinase interacting proteins 1 and 2 (GIT-1 and GIT-2) are highly conserved, ubiquitous scaffold proteins involved in localized signaling to help regulate focal contact assembly and cytoskeletal dynamics. GIT proteins contain multiple interaction domains that allow interaction with small GTPases (including ARF, Rac and cdc42), kinases (such as PAK and MEK), the Rho family GEF PIX, and the focal adhesion protein paxillin (reviewed in 1). GIT-1 is localized to focal adhesions, cytoplasmic complexes and membrane protrusions, and regulates cell protrusion formation and cell migration. GIT-1 has also been implicated in neuronal functions including synapse formation and the pathology of Huntington disease. Huntington disease is a genetic neurodegenerative condition involving a mutation in the huntington gene. The huntington gene product (htt) is ubiquitinated and degraded in human Huntington disease brains. Htt interacts directly with GIT-1 causing enhanced htt proteolysis, indicating that GIT-1 distribution and function may contribute to Huntington disease pathology..

Human, Mouse, Rat

See Manual

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