APC Anti-CXCR4/CD184 抗体 [12G5]
APC Anti-CXCR4/CD184 antibody [12G5]
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Anti-CXCR4/CD184 antibody [12G5] conjugated to APC - suitable for flow cytometry, and reacts with human samples. Clone [12G5] is a mouse monoclonal antibody and one of the most commonly used clones for flow cytometry.
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別名を表示する
CD184, C-X-C chemokine receptor type 4, CXC-R4, CXCR-4, FB22, Fusin, HM89, LCR1, Leukocyte-derived seven transmembrane domain receptor, Lipopolysaccharide-associated protein 3, NPYRL, Stromal cell-derived factor 1 receptor, LESTR, LAP-3, LPS-associated protein 3, SDF-1 receptor, CXCR4
- Flow Cyt
Supplier Data
Flow Cytometry - APC Anti-CXCR4/CD184 antibody [12G5] (AB270635)
Flow cytometric analysis of human peripheral whole blood cells labeling CD184 using ab270635, with the concentration of 10 μl reagent /100 μl of peripheral whole blood.
- Flow Cyt
Supplier Data
Flow Cytometry - APC Anti-CXCR4/CD184 antibody [12G5] (AB270635)
Flow cytometric analysis of lymphocytes (red) and monocytes (black) cells labeling CD184 using ab270635. Concentration of 10 μl reagent/100μl peripheral whole blood.
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Reactivity data
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補足情報
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
CXCR4 plays an important role in the immune system hematopoiesis and angiogenesis. It does not function alone and is often part of a larger protein complex where it recruits and activates other G proteins. The receptor mediates chemotactic responses directing cells to sites of inflammation or injury. Its interaction with CXCL12 is critical for maintaining immune surveillance aiding in the movement and positioning of immune cells.
Pathways
CXCR4 integrates into significant cellular signaling pathways such as the PI3K/AKT pathway and the MAPK pathway. It collaborates closely with signaling proteins like AKT1 and MAPK1 impacting cell survival and growth. These pathways are essential for various cellular functions including cell cycle progression and apoptosis regulation. The cross-talk between CXCR4 and these pathways underlines its influence on cell fate decisions.
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