GIT1 Antibody (924640) [Alexa Fluor® 405] Summary
E. coli-derived recombinant human GIT1
Ser485-Asp636
Accession # Q9Y2X7
Ser485-Asp636
Accession # Q9Y2X7
Detects human GIT1 in direct ELISAs and human, mouse, and rat GIT1 in Western blots.
IgG2b
Monoclonal
Mouse
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Applications/Dilutions
- Intracellular Staining by Flow Cytometry 0.25-1 ug/10^6 cells
Packaging, Storage & Formulations
Store the unopened product at 2 – 8 °C. Do not use past expiration date.
Supplied 0.2 mg/mL in a saline solution containing BSA and Sodium Azide.
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for GIT1 Antibody (924640) [Alexa Fluor® 405]
- 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 interactor 1
- G protein-coupled receptor kinase-interactor 1
- GIT1
- GRK-interacting protein 1
Background
GIT1 (ARF GTPase-activating protein GIT1) is a 95 kDa protein that belongs to ADP ribosylation factor family and is localized to focal adhesions, cytoplasmic complexes and membrane protrusions, and regulates cell protrusion formation and cell migration. G-protein coupled receptor (GPCR) kinase interacting proteins 1 and 2 (GIT1 and GIT2) 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. GIT1 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 GIT1 causing enhanced htt proteolysis, indicating that GIT1 distribution and function may contribute to Huntington disease pathology. Within amino acids (aa) 485-636, human and mouse GIT1 share 93% aa sequence identity.
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.