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Recombinant Human PLEKHG4 cell lysate

Cat.No. : PLEKHG4-1376HCL
  • Specification
  • Gene Information
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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;

For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.

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