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The protein encoded by PSPH belongs to a subfamily of the phosphotransferases. Additionally we are shipping Phosphoserine Phosphatase Proteins (19) and Phosphoserine Phosphatase Kits (3) and many more products for this protein.
Showing 10 out of 111 products:
Mouse (Murine) Polyclonal PSPH Primary Antibody for WB - ABIN1881701
Veiga-da-Cunha, Collet, Prieur, Jaeken, Peeraer, Rabbijns, Van Schaftingen: Mutations responsible for 3-phosphoserine phosphatase deficiency. in European journal of human genetics : EJHG 2004
Show all 3 references for ABIN1881701
Human Monoclonal PSPH Primary Antibody for EIA, IHC (p) - ABIN317526
Kim, Heo, Kim, Park, Moon, Kim, Kwon, Yoon, Shin, Jeong, Park, Lee, Jeon, Ro, Cho, Hwang: Molecular basis for the local conformational rearrangement of human phosphoserine phosphatase. in The Journal of biological chemistry 2002
Show all 2 references for ABIN317526
Human Polyclonal PSPH Primary Antibody for WB - ABIN2786785
Ewing, Chu, Elisma, Li, Taylor, Climie, McBroom-Cerajewski, Robinson, OConnor, Li, Taylor, Dharsee, Ho, Heilbut, Moore, Zhang, Ornatsky, Bukhman, Ethier, Sheng, Vasilescu, Abu-Farha, Lambert, Duewel et al.: Large-scale mapping of human protein-protein interactions by mass spectrometry. ... in Molecular systems biology 2007
Human Polyclonal PSPH Primary Antibody for ELISA, WB - ABIN451753
Veeranna, Shetty: Phosphoserine phosphatase of human brain: partial purification, characterization, regional distribution, and effect of certain modulators including psychoactive drugs. in Neurochemical research 1991
PSP, comprises eight exons and seven introns, is strongly expressed in parotid glands, but is not present in heart, liver, lung, kidney, muscle, or stomach.
We further uncovered that phosphoserine phosphatase (PSPH), the final rate-limiting enzyme of the SSP pathway, is critical for cMyc (show MYC Antibodies)-driven cancer progression both in vitro and in vivo
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
phosphoserine phosphatase deficiency is associated with Neu-Laxova syndrome.
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
human phosphoserine phosphatase structure now shows a sevenfold coordinated Ca(2 (show CA2 Antibodies)+) ion in the active site that might explain the inhibitory effect of Ca(2 (show CA2 Antibodies)+) on the enzyme
PSP (show BPIFA2 Antibodies) has a role in neural stem cell proliferation and may regulate signaling between neural stem cells and other cells within the stem cell niche.
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.
, parotid secretory protein
, O-phosphoserine phosphohydrolase
, L-3-phosphoserine phosphatase