Flow cytometric analysis of C57BL/6 mouse splenocytes labeling Mouse CD197 (CCR7) at 1/200 (1 μg) dilution / (Right panel) compared with a Rat IgG, Isotype Control / (Left panel). Goat Anti - Rat IgG Alexa Fluor® 488 was used as the secondary antibody. Then cells were stained with CD3 - Brilliant Violet 421™ separately. Gated on total viable cells.
Product Details
Product Details
Product Specification
Host | Rat |
Antigen | CD197 (CCR7) |
Synonyms | C-C chemokine receptor type 7; C-C CKR-7; CC-CKR-7; Epstein-Barr virus-induced G-protein coupled receptor 1 (EBI1; EBV-induced G-protein coupled receptor 1); MIP-3 beta receptor; Cmkbr7; Ebi1; Ebi1h |
Location | Cell membrane |
Accession | P47774 |
Clone Number | S-R528 |
Antibody Type | Rat mAb |
Isotype | IgG2a,k |
Application | FCM |
Reactivity | Ms |
Purification | Protein G |
Concentration | 2 mg/ml |
Conjugation | Unconjugated |
Physical Appearance | Liquid |
Storage Buffer | PBS pH7.4 |
Stability & Storage | 12 months from date of receipt / reconstitution, 2 to 8 °C as supplied. |
Dilution
application | dilution | species |
FCM | 1:200 | Ms |
Background
CD197, also known as CCR7 or BLR2, is a protein that belongs to the G protein-coupled receptor family and is a subset of chemokines. It is identified as being induced by the Epstein-Barr virus (EBV) and is considered a mediator of the effects of EBV on B lymphocytes. CCR7 is expressed in blood, bone marrow, lymph nodes, and the gastrointestinal tract, particularly on lymphoid tissues and activated B and T lymphocytes. It has been shown to control the migration of memory T cells to inflamed tissues and the maturation of dendritic cells. The chemokine (C-C motif) ligand 19 (CCL19/ECL) is reported to be a specific ligand for this receptor. CD197 is involved in the cellular response to cytokine stimuli, myeloid dendritic cell chemotaxis, and the positive regulation of neutrophil chemotaxis. In the context of T cell maturation, CD197 is expressed on recent thymic emigrants (RTEs) that mature into naive T lymphocytes. These cells differentiate into short-term effector T cells and further into memory T cells, which include central memory T cells (expressing CCR7 and CD62L) and effector memory T cells (which do not migrate to lymph nodes). In cancer immunology, particularly in lung cancer, the presence of memory T cells in metastatic lymph nodes has been shown to be an independent positive prognostic factor. Tregs, which play a significant role in regulating the immune response to tumors, can be differentiated into naive, effector, and terminal effector subtypes based on the expression of the CD45RO marker.
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