Recombinant Human PTPRM protein is a Human Fragment protein, in the 764 to 1452 aa range, expressed in Baculovirus infected Sf9, with >90% purity and suitable for WB.
Application | Reactivity | Dilution info | Notes |
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Application WB | Reactivity Reacts | Dilution info - | Notes - |
Receptor protein-tyrosine phosphatase that mediates homotypic cell-cell interactions and plays a role in adipogenic differentiation via modulation of p120 catenin/CTNND1 phosphorylation (PubMed:10753936, PubMed:17761881). Promotes CTNND1 dephosphorylation and prevents its cytoplasmic localization where it inhibits SLC2A4 membrane trafficking. In turn, SLC2A4 is directed to the plasma membrane and performs its glucose transporter function (PubMed:21998202).
PTPRL1, PTPRM, Receptor-type tyrosine-protein phosphatase mu, Protein-tyrosine phosphatase mu, R-PTP-mu
Recombinant Human PTPRM protein is a Human Fragment protein, in the 764 to 1452 aa range, expressed in Baculovirus infected Sf9, with >90% purity and suitable for WB.
pH: 7.5
Constituents: 25% Glycerol (glycerin, glycerine), 0.87% Sodium chloride, 0.79% Tris HCl, 0.00385% (R*,R*)-1,4-Dimercaptobutan-2,3-diol, 0.00174% PMSF
Purity was determined to be >90% by densitometry. Affinity purified.
Receptor protein-tyrosine phosphatase that mediates homotypic cell-cell interactions and plays a role in adipogenic differentiation via modulation of p120 catenin/CTNND1 phosphorylation (PubMed:10753936, PubMed:17761881). Promotes CTNND1 dephosphorylation and prevents its cytoplasmic localization where it inhibits SLC2A4 membrane trafficking. In turn, SLC2A4 is directed to the plasma membrane and performs its glucose transporter function (PubMed:21998202).
Belongs to the protein-tyrosine phosphatase family. Receptor class 2B subfamily.
PTPRM also known as Protein Tyrosine Phosphatase Receptor Type M or RPTPmu is a transmembrane protein that acts mechanically by dephosphorylating tyrosine residues on target proteins. This protein weighs approximately 155 kDa. PTPRM displays expression mainly in the brain and epithelial tissues. It is comprised of an extracellular segment a transmembrane domain and an intracellular segment with catalytic activity. Its role involves facilitating cell-cell adhesion through homophilic interactions significantly impacting signaling events that regulate cellular processes.
Within the human cells PTPRM plays a vital role in controlling cell adhesion migration and signaling. As part of the leukocyte common antigen-related (LAR) phosphatase family this protein collaborates with other proteins to modulate cellular junction integrity and movement. The extracellular domain of PTPRM participates in cellular communication while its intracellular catalytic property dephosphorylates signaling molecules to fine-tune cellular responses. These activities highlight its importance in maintaining tissue organization and signaling networks.
PTPRM is involved in the regulation of the cadherin signaling pathway and MAPK signaling pathway. Through its interactions it modulates E-cadherin-mediated adhesion complexes where it cooperates closely with proteins like β-catenin to regulate adhesion strength and cell position. Additionally PTPRM influences the MAPK signaling cascade affecting cell proliferation and differentiation processes. By fine-tuning these pathways PTPRM plays a significant role in ensuring normal cellular function and communication.
Mutations or dysregulations in PTPRM can be associated with cancer particularly colorectal carcinoma and neurological disorders like epilepsy. In colorectal cancer PTPRM's interaction with E-cadherin is particularly affected influencing tumor growth and metastasis. In neurological pathways PTPRM's regulation of signaling proteins like SRC can play significant roles. Alterations in these pathways may lead to abnormal neuronal signaling implicated in epilepsy highlighting the importance of PTPRM in maintaining healthy cellular function and preventing disease.
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SDS-PAGE showing ab71346 at approximately 110kDa.
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