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PTPN22 encodes of member of the non-receptor class 4 subfamily of the protein-tyrosine phosphatase family. Additionally we are shipping PTPN22 Proteins (4) and PTPN22 Kits (1) and many more products for this protein.
Showing 10 out of 65 products:
Human Polyclonal PTPN22 Primary Antibody for EIA, WB - ABIN954376
Bianco, Verreschi, Oliveira, Guedes, Galera, Galera, Barbosa, Lipay: PTPN22 polymorphism is related to autoimmune disease risk in patients with Turner syndrome. in Scandinavian journal of immunology 2010
Show all 3 references for ABIN954376
Human Polyclonal PTPN22 Primary Antibody for WB - ABIN525622
Cao, Yang, Colby, Hogan, Hu, Jennette, Berg, Zhang, Jennette, Falk, Preston: High basal activity of the PTPN22 gain-of-function variant blunts leukocyte responsiveness negatively affecting IL-10 production in ANCA vasculitis. in PLoS ONE 2012
our data suggest a critical role for GITR (show TNFRSF18 Antibodies) in Treg cell homeostasis and indicate that Ptpn22 independently affects the differentiation status of Treg cells and their homeostatic behavior
Tec (show NR4A3 Antibodies) enhances c-Maf (show MAF Antibodies)-dependent IL-4 (show IL4 Antibodies) promoter activity. This effect of Tec (show NR4A3 Antibodies) is counteracted by Ptpn22, which physically interacts with and facilitates tyrosine dephosphorylation of c-Maf (show MAF Antibodies) thereby attenuating its transcriptional activity.
lack of PTPN22 strengthens transplant tolerance to pancreatic islets by expanding both FOXP3 (show FOXP3 Antibodies)(+) Treg and Tr1 (show TXNRD1 Antibodies) cells
Ptpn22 and Cd2 (show CCND2 Antibodies) Variations Are Associated with Altered Protein Expression and Susceptibility to Type 1 Diabetes
T cell activation modulates the expression of PTPN22 and additional inhibitory phosphatases.
PTPN22 is an inhibitor of PAD-4 (show PADI4 Antibodies) and protein citrullination.
Autoimmunity-associated protein tyrosine phosphatase (show ACP1 Antibodies) PEP (show PREP Antibodies) negatively regulates IFN-alpha (show IFNA Antibodies) receptor signaling.
lack of Ptpn22 exacerbates virally-induced type 1 diabetes in lymphocytic choriomeningitis virus mice, while maintaining higher number of Treg cells in the antiviral response in the blood and spleen but not in the pancreatic lymph nodes
Data suggest that a gain-of-function of human PTPN22 transgene encoding the tyrosine phosphatase LYP is unlikely to increase risk of autoimmunity through alterations of thymic selection.
PTPN22 limited signaling via the T cell antigen receptor (TCR) by weak agonists and self antigens while not impeding responses to strong agonist antigens.
sex-specific pattern of association is broadly applicable to different populations, and provides further impetus to undertake mechanistic studies to understand the impact of sex on PTPN22 in JIA.
PTPN22 gene variants were associated with type 1 diabetes susceptibility and autoimmune polyglandular syndrome type III.
Our results do not support association between PTPN22/CSK (show CSK Antibodies) and Henoch-Schonlein purpura
The findings suggest that PTPN22 polymorphisms may predispose the chronicity or the development of cirrhosis and hepatocellular carcinoma in HBV infection.
The association of PTPN22 rs2476601 with juvenile idiopathic arthritis is specific to females
rs56048322 was significantly associated with type 1 diabetes. rs56048322 affects splicing, resulting in a novel isoform of LYP which competes with the wild-type for binding to CSK (show CSK Antibodies) and results in hyporesponsiveness of CD4 (show CD4 Antibodies)+ T cells to antigen stimulation.
role of PTPN22 in type 1 diabetes and Crohn's disease (review
a significant association between PTPN22 R620W polymorphism and MG risk: PTPN22 R620W polymorphism showed increased early-onset myasthenia gravis (EOMG) risk (OR=2.38; 95% CI, 1.52-3.71; I(2)=0%)(Meta-Analysis)
ADA6, PTPN22 and ACP1 (show ACP1 Antibodies) are involved in immune reactions: since endometriosis has an autoimmune component.
suggests that the rs2476601 polymorphism of PTPN22 gene is mono-morphic in Iranian population, containing only C allele
This gene encodes of member of the non-receptor class 4 subfamily of the protein-tyrosine phosphatase family. The encoded protein is a lymphoid-specific intracellular phosphatase that associates with the molecular adapter protein CBL and may be involved in regulating CBL function in the T-cell receptor signaling pathway. Mutations in this gene may be associated with a range of autoimmune disorders including Type 1 Diabetes, rheumatoid arthritis, systemic lupus erythematosus and Graves' disease. Alternatively spliced transcript variants encoding distinct isoforms have been described.
PEST domain-enriched tyrosine phosphatase
, hematopoietic cell protein-tyrosine phosphatase 70Z-PEP
, protein tyrosine phosphatase, non-receptor type 8
, tyrosine-protein phosphatase non-receptor type 22
, PEST-domain phosphatase
, lymphoid phosphatase
, lymphoid-specific protein tyrosine phosphatase