Comparison

CD45RB [MEM-55] (FITC)

Item no. 20-272-191665
Manufacturer GENWAY
Amount 100 TESTS
Category
Type Antibody
Clone MEM-55
Specific against other
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias GWB-83D1A0
Similar products 20-272-191665
Available
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.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 100 TESTS
Available: In stock
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