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Recombinant pig IL-2 Protein (Active) (RMPP-00230537)

Cat. No.: RMPP-00230537

Category: Recombinant Protein

Research Area: Immunology

INQUIRY 20 μg 1 mg

Product Features

Source E.coli
Purity > 95% SDS-PAGE.
Nature Recombinant
Endotoxin Level < 1.000 Eu/µg
Animal Free No
Tags His-DDDDK tag N-Terminus
Form Liquid
Applications MS; SDS-PAGE
Key Features Expression system: E.coli; Purity: > 95% SDS-PAGE; Endotoxin level: < 1.000 Eu/µg; Tags: His-DDDDK tag N-Terminus; Suitable for: MS, SDS-PAGE

Protein Information

UniProt ID P08575
Molecular Weight 30 kDa including tags
Sequence MRGSHHHHHH GMASMTGGQQ MGRDLYDDDD KDRWGSVMIA AQGPLKETIG DFWQMIFQRK VKVIVMLTEL KHGDQEICAQ YWGEGKQTYG
DIEVDLKDTD KSSTYTLRVF ELRHSKRKDS RTVYQYQYTN WSVEQLPAEP KELISMIQVV KQKLPQKNSS EGNKHHKSTP LLIHCRDGSQ
QTGIFCALLN LLESAETEEV VDIFQVVKAL RKARPGMVST FEQYQFLYDV IASTYPAQNG QVKKNNHQED KIEFDNE
Sequence Similarities Belongs to the protein-tyrosine phosphatase family. Receptor class 1/6 subfamily. Contains 2 fibronectin type-III domains. Contains 2 tyrosine-protein phosphatase domains.
Protein Length Protein fragment
Cellular Localization Membrane. Membrane raft. Colocalized with DPP4 in membrane rafts.
Domain The first PTPase domain interacts with SKAP1.
Function Protein tyrosine-protein phosphatase required for T-cell activation through the antigen receptor. Acts as a positive regulator of T-cell coactivation upon binding to DPP4. The first PTPase domain has enzymatic activity, while the second one seems to affect the substrate specificity of the first one. Upon T-cell activation, recruits and dephosphorylates SKAP1 and FYN.
Involvement in Disease Defects in PTPRC are a cause of severe combined immunodeficiency autosomal recessive T-cell-negative/B-cell-positive/NK-cell-positive (T(-)B(+)NK(+) SCID). A form of severe combined immunodeficiency (SCID), a genetically and clinically heterogeneous group of rare congenital disorders characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. Patients present in infancy recurrent, persistent infections by opportunistic organisms. The common characteristic of all types of SCID is absence of T-cell-mediated cellular immunity due to a defect in T-cell development.Genetic variations in PTPRC are involved in multiple sclerosis susceptibility (MS). MS is a neurodegenerative disorder characterized by the gradual accumulation of focal plaques of demyelination particularly in the periventricular areas of the brain. Peripheral nerves are not affected. Onset usually in third or fourth decade with intermittent progression over an extended period. The cause is still uncertain.
Post-translational Modifications Heavily N- and O-glycosylated.

Storage & Shipping

Shipping and Storage Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
pH: 8.00Constituents: 0.32% Tris HCl, 0.88% Sodium chloride, 10% Glycerol (glycerin, glycerine), 0.02% DTT

For research use only. Not for clinical use.