PAK1 / Unconjugated /
Product Details
| Description | Rabbit polyclonal to PAK1.p21-activated kinase 1 (PAK1) belongs to the protein kinase superfamily, STE Ser/Thr protein kinasefamily and STE20 subfamily. PAK1 can be activated by CDC42 and RAC1, and is likely the GTPaseeffector that links the Rho-related GTPases to the JNK MAP kinase pathway. PAK1 is involved in thedissolution of stress fibers and reorganization of focal complexes, as well as in the regulation ofmicrotubule biogenesis through phosphorylation of TBCB. DVL1 and PAK1 form a ternary complexwith MUSK which is important for MUSK-dependent regulation of AChR clustering during theformation of the neuromuscular junction (NMJ). The activity of PAK1 is inhibited in cells undergoingapoptosis, potentially due to binding of CDC2L1 and CDC2L2. - | |
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| Conjugate | Unconjugated | |
| Clone | ||
| Target Species | Human, Mouse | |
| Applications | WB | |
| Supplier | Biorbyt | |
| Catalog # | Sign in to view product details, citations, and spectra | |
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About PAK1
This gene encodes a family member of serine/threonine p21-activating kinases, known as PAK proteins. These proteins are critical effectors that link RhoGTPases to cytoskeleton reorganization and nuclear signaling, and they serve as targets for the small GTP binding proteins Cdc42 and Rac. This specific family member regulates cell motility and morphology. Mutations in this gene have been associated with macrocephaly, seizures, and speech delay. Overexpression of this gene is also reported in many cancer types, and particularly in breast cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2020]
This gene encodes a family member of serine/threonine p21-activating kinases, known as PAK proteins. These proteins are critical effectors that link RhoGTPases to cytoskeleton reorganization and nuclear signaling, and they serve as targets for the small GTP binding proteins Cdc42 and Rac. This specific family member regulates cell motility and morphology. Mutations in this gene have been associated with macrocephaly, seizures, and speech delay. Overexpression of this gene is also reported in many cancer types, and particularly in breast cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2020]
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