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人 PHLPP1 抗体对
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人 PHLPP1 抗体对

01AB02252

PH domain and leucine rich repeat protein phosphatase 1 (PHLPP1) is a magnesium/manganese-dependent serine/threonine phosphatase that serves as a critical regulator of cell signaling. It specifically dephosphorylates the hydrophobic motif of various AGC kinases, including Akt2/3, PKC alpha/beta, and S6K1, as well as nuclear substrates like STAT1 and histones. By inactivating these targets, PHLPP1 functions as a broad tumor suppressor that dampens the PI3K-Akt and RAS-ERK pathways, thereby limiting cell proliferation and promoting apoptosis. It also modulates metabolic and immune signaling through the repression of receptor tyrosine kinase transcription. Clinically, the loss or dysregulation of PHLPP1 is linked to multiple cancers, including prostate and hematologic malignancies, and is associated with the development of obesity and type 2 diabetes due to impaired insulin signaling.

Human
规格起售价
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技术参数

靶点基因名
PHLPP1
基因别名
KIAA0606; PHLPP; PLEKHE1; SCOP
蛋白别名
PH domain and leucine rich repeat protein phosphatase 1; PHLPP1
UniProt
O60346
物种
Human

产品详情

靶点名称
PHLPP1
蛋白名称
PH domain and leucine rich repeat protein phosphatase 1
蛋白别名
PH domain leucine-rich repeat-containing protein phosphatase 1; Pleckstrin homology domain-containing family E member 1; PH domain-containing family E member 1; Suprachiasmatic nucleus circadian oscillatory protein; hSCOP
靶点基因名
PHLPP1
基因别名
KIAA0606; PHLPP; PLEKHE1; SCOP
UniProt
O60346
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

PH domain and leucine rich repeat protein phosphatase 1 (PHLPP1) is a magnesium/manganese-dependent serine/threonine phosphatase that serves as a critical regulator of cell signaling. It specifically dephosphorylates the hydrophobic motif of various AGC kinases, including Akt2/3, PKC alpha/beta, and S6K1, as well as nuclear substrates like STAT1 and histones. By inactivating these targets, PHLPP1 functions as a broad tumor suppressor that dampens the PI3K-Akt and RAS-ERK pathways, thereby limiting cell proliferation and promoting apoptosis. It also modulates metabolic and immune signaling through the repression of receptor tyrosine kinase transcription. Clinically, the loss or dysregulation of PHLPP1 is linked to multiple cancers, including prostate and hematologic malignancies, and is associated with the development of obesity and type 2 diabetes due to impaired insulin signaling.