ArtNr |
20-272-192779 |
Hersteller |
GENWAY
|
Menge |
0.1 mg |
Kategorie |
|
Typ |
Antibody |
Applikationen |
WB, IP, IHC |
Clon |
MEM-28 |
Specific against |
other |
ECLASS 10.1 |
32160702 |
ECLASS 11.0 |
32160702 |
UNSPSC |
12352203 |
Alias |
GWB-14FA21 |
Similar products |
20-272-192779 |
Lieferbar |
|
Genway ID: |
GWB-14FA21 |
Clone: |
MEM-28 |
Isotype: |
IgG1 |
Immunogen: |
Tissue / cell preparation (Human). (Thymocytes and T lymphocytes). |
Antigen Species: |
Human |
Specificity: |
This product reacts with all alternative forms of human CD45 antigen (Leukocyte Common Antigen) a 180-220 kDa single chain type I transmembrane protein expressed at high level on all cells of hematopoietic origin except erythrocytes and platelets. |
Positive Control: |
Jurkat human leukemia T-cell lysate and Kg-1a human leukemia T-cell lysate |
Target: |
CD45 |
Localization: |
Type I membrane protein |
Concentration: |
1 mg/ml |
Purification Note: |
From mouse ascitic fluid. Storage |
Buffer: |
Phosphate buffered saline pH 7. 4 containing 15mM sodium azide |
Application Note: |
For IHC-P: Use at an assay dependent dilution. No pre-treatment of tissue sections is essential. For WB: Use at a concentration of 2 µ g/ml. Not tested in other applications. Optimal dilutions/concentrations should be determined by the researcher. Cellular |
Localization: |
Type I membrane protein CD45 is a family of single chain transmembraneous glycoproteins consisting of at least four isoforms which share a common large intracellular domain. Their extracellular domains are heavily glycosylated. The different isoforms are produced by alternative messenger RNA splicing of three exons of a single gene on chromosome 1. CD45 is expressed on cells of the human hematopoietic lineage with the exception of mature red cells. It is not detected on differentiated cells of other tissues. It is likely that CD45 plays an important role in signal transduction inhibition or upregulation of various immunological functions. |
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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