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Recombinant Human PSPH cell lysate

Cat.No.: PSPH-1430HCL
Description: The protein encoded by this gene belongs to a subfamily of the phosphotransferases. This encoded enzyme is responsible for the third and last step in L-serine formation. It catalyzes magnesium-dependent hydrolysis of L-phosphoserine and is also involved in an exchange reaction between L-serine and L-phosphoserine. Deficiency of this protein is thought to be linked to Williams syndrome.
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: PSPH phosphoserine phosphatase [ Homo sapiens ]
Official Symbol: PSPH
Synonyms: PSPH; phosphoserine phosphatase; PSP; PSPase; L-3-phosphoserine phosphatase; O-phosphoserine phosphohydrolase; PSPHD;
Gene ID: 5723
mRNA Refseq: NM_004577
Protein Refseq: NP_004568
MIM: 172480
UniProt ID: P78330
Chromosome Location: 7p11.2
Pathway: Amino acid synthesis and interconversion (transamination), organism-specific biosystem; Glycine, serine and threonine metabolism, organism-specific biosystem; Glycine, serine and threonine metabolism, conserved biosystem; Metabolic pathways, organism-specific biosystem; Metabolism, organism-specific biosystem; Metabolism of amino acids and derivatives, organism-specific biosystem; Serine biosynthesis, organism-specific biosystem;
Function: calcium ion binding; hydrolase activity; magnesium ion binding; phosphoserine phosphatase activity; phosphoserine phosphatase activity; protein homodimerization activity;

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