ArtNr |
20-272-191665 |
Hersteller |
GENWAY
|
Menge |
100 TESTS |
Kategorie |
|
Typ |
Antibody |
Clon |
MEM-55 |
Specific against |
other |
ECLASS 10.1 |
32160702 |
ECLASS 11.0 |
32160702 |
UNSPSC |
12352203 |
Alias |
GWB-83D1A0 |
Similar products |
20-272-191665 |
Lieferbar |
|
Genway ID: |
GWB-83D1A0 |
Clone: |
MEM-55 |
Isotype: |
IgG1 |
Immunogen: |
Thymocytes and T lymphocytes (Human). |
Antigen Species: |
Human |
Specificity: |
Mouse monoclonal [MEM-55] to CD45RB recognizes a siliadase-sensitive epitope of CD45RB antigen. |
Target: |
CD45RB |
Localization: |
Cell Membrane |
Conjugation: |
FITC |
Purification Note: |
Unconjugated FITC is removed by dialysis. Storage |
Preservative: |
15mM Sodium Azide. Constituents: PBS BSA. pH 7. 4 |
Application Note: |
FACS: 1/5. Use 20µ l per 100µ l whole blood. Not tested in other applications. Optimal dilutions/concentrations should be determined by the end user. Cellular |
Localization: |
Cell Membrane CD45RB is an alternatively spliced form of CD45 a cell surface glycoprotein. It is expressed on on peripheral B cells T cytotoxic cells and CD4+ T cells. It has a role in cell signalling regulation through the activation of the Src family of tyrosine kinases. |
Function: |
Required for T-cell activation through the antigen receptor. 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 an dephosphorylates SKAP1 and FYN. |
Catalytic Activity: |
Protein tyrosine phosphate + H2O = protein tyrosine + phosphate. |
Subunit: |
Binds GANAB and PRKCSH (By similarity). Interacts with SKAP1. |
Subcellular Location: |
Membrane; Single-pass type I membrane protein. |
Domain: |
The first PTPase domain interacts with SKAP1. |
Ptm: |
Heavily N- and O-glycosylated. |
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) [MIM:608971]. SCID refers to 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 with SCID present in infancy with 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. |
Disease: |
Genetic variations in PTPRC are involved in multiple sclerosis susceptibility (MS) [MIM:126200]. 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. |
Similarity: |
Belongs to the protein-tyrosine phosphatase family. Receptor class 1/6 subfamily. |
Similarity: |
Contains 2 fibronectin type-III domains. |
Similarity: |
Contains 2 tyrosine-protein phosphatase domains. |
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