Iright
BRAND / VENDOR: CST

CST, 2919S, GIT-1 Antibody

CATALOG NUMBER: 2919S
Regular price$0.99
/
Shipping calculated at checkout.
  • In stock, ready to ship

  • Backordered, shipping soon

This site is protected by hCaptcha and the hCaptcha Privacy Policy and Terms of Service apply.

Product Description
Polyclonal Antibody for studying GIT1. Validated for Western Blotting,Immunoprecipitation. Highly specific and rigorously validated in-house, GIT-1 Antibody (CST #2919) is ready to ship. Product Usage Information Western Blotting: 1:1000 Immunoprecipitation: 1:100 Storage Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA and 50% glycerol. Store at -20°C. Do not aliquot the antibody. Protocol Available protocols: Western Blotting, Immunoprecipitation Specificity / Sensitivity GIT-1 Antibody recognizes endogenous levels of total GIT-1 protein. Species Reactivity: Human, Mouse, Rat, Hamster, Monkey, Bovine Source / Purification Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to residues near the carboxy terminus of human GIT-1. Antibodies are purified using peptide affinity chromatography. Background 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 (reviewed in 1). GIT1 is localized to focal adhesions, cytoplasmic complexes and membrane protrusions, and regulates cell protrusion formation and migration (2). GIT1 has also been implicated in neuronal functions including synapse formation (3) and the pathology of Huntington's disease (HD) (4). HD is a genetic neurodegenerative condition involving a mutation in the gene encoding the protein huntingtin. Huntingtin is ubiquitinated and degraded in human HD brains (5). Huntingtin interacts directly with GIT1, causing enhanced proteolysis and indicating that GIT1 distribution and function may contribute to HD pathology (4). Alternate Names ARF GAP GIT1; ARF GTPase-activating protein GIT1; CAT-1; CAT1; 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; GIT ArfGAP 1; GIT1; GRK-interacting protein 1 Specification REACTIVITY: H M R Hm Mk B SENSITIVITY: Endogenous MW (kDa): 95 SOURCE: Rabbit

Order Guidelines

1. Price & Stock Available on Request. 📧Click to send email to: service@iright.com

2. Please DO NOT make payment before confirmation.

3. Minimum order value of $1,000 USD required.

Collaboration

Tony Tang

📧Email: Tony.Tang@iright.com

📱Mobile/WhatsApp/Wechat: +86-17717886924