"PLEKHG4" Related Products

Recombinant Human PLEKHG4 cell lysate

Cat.No.: PLEKHG4-1376HCL
Description: The protein encoded by this gene contains multiple domains suggestive of a role in intracellular signaling and cytoskeleton dynamics at the Golgi apparatus. Mutations in this gene are associated with spinocerebellar ataxia 16q22-linked. Several alternatively spliced transcript variants, differing only in the 5 UTR, or encoding a different isoform, have been found for this gene.
Species: Human
Size: 100 ul
Storage Buffer: 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
Applications: Western Blot;
Gene Name: PLEKHG4 pleckstrin homology domain containing, family G (with RhoGef domain) member 4 [ Homo sapiens ]
Official Symbol: PLEKHG4
Synonyms: PLEKHG4; pleckstrin homology domain containing, family G (with RhoGef domain) member 4; SCA4, spinocerebellar ataxia 4; puratrophin-1; ARHGEF44; DKFZP434I216; puratrophin 1; PH domain-containing family G member 4; Purkinje cell atrophy associated protein 1; Purkinje cell atrophy-associated protein 1; pleckstrin homology domain-containing family G member 4; SCA4; PRTPHN1; DKFZp434I216;
Gene ID: 25894
mRNA Refseq: NM_001129727
Protein Refseq: NP_001123199
MIM: 609526
UniProt ID: Q58EX7
Chromosome Location: 16q22.1
Function: Rho guanyl-nucleotide exchange factor activity; guanyl-nucleotide exchange factor activity;

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