PSPH Antibody

Code CSB-PA018938GA01HU
Size $600
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Product Details

Uniprot No.
Target Names
PSPH
Alternative Names
EC 3.1.3.3 antibody; L 3 phosphoserine phosphatase antibody; L-3-phosphoserine phosphatase antibody; O phosphoserine phosphohydrolase antibody; O-phosphoserine phosphohydrolase antibody; Phosphoserine phosphatase antibody; Phosphoserine phosphatase deficiency; included antibody; PSP antibody; PSPase antibody; Psph antibody; PSPHD antibody; SERB_HUMAN antibody
Raised in
Rabbit
Species Reactivity
Human,Mouse,Rat
Immunogen
Human PSPH
Immunogen Species
Homo sapiens (Human)
Isotype
IgG
Purification Method
Antigen Affinity purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
PBS with 0.02% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
Tested Applications
ELISA,WB
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

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Target Background

Function
Catalyzes the last irreversible step in the biosynthesis of L-serine from carbohydrates, the dephosphorylation of O-phospho-L-serine to L-serine. L-serine can then be used in protein synthesis, to produce other amino acids, in nucleotide metabolism or in glutathione synthesis, or can be racemized to D-serine, a neuromodulator. May also act on O-phospho-D-serine (Probable).
Gene References into Functions
  1. PSPH expression is a novel biomarker for poor prognosis and could play an important role in tumor progression of colorectal cancer. PMID: 28476802
  2. We further uncovered that phosphoserine phosphatase (PSPH), the final rate-limiting enzyme of the SSP pathway, is critical for cMyc-driven cancer progression both in vitro and in vivo PMID: 25793315
  3. study of an intellectual disability family from Pakistan; identified a variant in PSPH: chr7:56088803C>T, NM_004577.3 c.103G>A; p.Ala35Thr (hg19) which segregated in homozygous form with the phenotype in both branches of the family PMID: 25080166
  4. phosphoserine phosphatase deficiency is associated with Neu-Laxova syndrome. PMID: 25152457
  5. status of PSPH in normal skin epidermis and skin tumors along with its sub-cellular localization in epidermal keratinocytes and its requirement for squamous cell carcinoma proliferation PMID: 21726982
  6. purification, crystallization and preliminary X-ray diffraction analysis PMID: 11752790
  7. description of the first crystal structures of the HPSP in complexes with the competitive inhibitor 2-amino-3-phosphonopropionic a PMID: 12213811
  8. human phosphoserine phosphatase structure now shows a sevenfold coordinated Ca(2+) ion in the active site that might explain the inhibitory effect of Ca(2+) on the enzyme PMID: 15291819

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Involvement in disease
Phosphoserine phosphatase deficiency (PSPHD)
Subcellular Location
Cytoplasm, cytosol.
Protein Families
HAD-like hydrolase superfamily, SerB family
Database Links

HGNC: 9577

OMIM: 172480

KEGG: hsa:5723

STRING: 9606.ENSP00000275605

UniGene: Hs.512656

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