Rac1 (Ras-related C3 Botulinum Toxin Substrate 1) (human) (rec.)

CHF 366.00
In stock
YIF-LF-P01410.2 mgCHF 366.00
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Product Details
Synonyms RAC1; MIG5; TC25; p21-Rac1; Ras-like Protein TC25; Cell Migration-inducing Gene 5 Protein; Ras-related C3 Botulinum Toxin Substrate 1
Product Type Protein
Properties
Source/Host E. coli
Crossreactivity Human
Purity ≥95% (SDS-PAGE)
Formulation Lyophilized from 50mM HEPES, pH8.0 / 10mM GSH.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

Declaration Manufactured by AbFrontier
Shipping and Handling
Shipping BLUE ICE
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Avoid freeze/thaw cycles.
Use/Stability After reconstitution, store at -80°C.
Documents
MSDS Inquire
Product Specification Sheet
Datasheet Download PDF

Rho-family GTPases, including Cdc42, Rac1 and RhoA, regulate actin cytoskeleton and cell adhesion and play a central role in establishing cell polarisation. They also play an important role in cell growth and differentiation as well as transcriptional regulation. Migrating vertebrate cells in tissue culture display a characteristic polarization of the actin cytoskeleton. The dynamic organization of the actin cytoskeleton provides the force for cell motility and is regulated by small GTPases of the Rho family, in particular Rac1, RhoA and Cdc42. Rac1 (Ras-related C3 botulinum toxin substrate 1) is a small (~21 kDa) GTPase, and is a member of the Rac subfamily of the family Rho family of GTPases. Rac can be activated by extracellular signals through various types of membrane receptors including receptor tyrosine kinases such as the PDGF receptor. Rac executes its biological functions through activating downstream effectors, such as PAK (p21-activated kinase). Rac plays critical roles in a wide variety of cell functions including cell cycle control, regulation of gene expression, activation of NADPH oxidase of phagocytic cells, actin cytoskeletal reorganization, axonal guidance and cell migration.

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