Rat Monoclonal CD44 antibody - conjugated to FITC. Suitable for Flow Cyt and reacts with Mouse samples. Cited in 8 publications.
pH: 7.4
Preservative: 0.1% Sodium azide
Constituents: PBS
Flow Cyt | |
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Mouse | Tested |
Species | Dilution info | Notes |
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Species Mouse | Dilution info 2 µg for 106 Cells | Notes ab18404 - Rat monoclonal IgG1, is suitable for use as an isotype control with this antibody. |
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Cell-surface receptor that plays a role in cell-cell interactions, cell adhesion and migration, helping them to sense and respond to changes in the tissue microenvironment (PubMed:16541107, PubMed:19703720, PubMed:22726066). Participates thereby in a wide variety of cellular functions including the activation, recirculation and homing of T-lymphocytes, hematopoiesis, inflammation and response to bacterial infection (PubMed:7528188). Engages, through its ectodomain, extracellular matrix components such as hyaluronan/HA, collagen, growth factors, cytokines or proteases and serves as a platform for signal transduction by assembling, via its cytoplasmic domain, protein complexes containing receptor kinases and membrane proteases (PubMed:18757307, PubMed:23589287). Such effectors include PKN2, the RhoGTPases RAC1 and RHOA, Rho-kinases and phospholipase C that coordinate signaling pathways promoting calcium mobilization and actin-mediated cytoskeleton reorganization essential for cell migration and adhesion (PubMed:15123640).
CD44, LHR, MDU2, MDU3, MIC4, CD44 antigen, CDw44, Epican, Extracellular matrix receptor III, GP90 lymphocyte homing/adhesion receptor, HUTCH-I, Heparan sulfate proteoglycan, Hermes antigen, Hyaluronate receptor, Phagocytic glycoprotein 1, Phagocytic glycoprotein I, ECMR-III, PGP-1, PGP-I
Rat Monoclonal CD44 antibody - conjugated to FITC. Suitable for Flow Cyt and reacts with Mouse samples. Cited in 8 publications.
pH: 7.4
Preservative: 0.1% Sodium azide
Constituents: PBS
Recognises all isoforms of CD44/pgp-1 (Mr 80-95 kDa)
ab25064 can inhibit hyaluronate-dependent cell aggregation, prevent lympho-hemopoiesis in both Dexter and Whitlock-Witte Cultures, prevent the earliest intrathymic precursors from homing to the thymus, and costimulate the activation of freshly purified splenic CD4+ T cells.
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ab25064 (at a concentration of 1 μg/106 cells) staining cells from BALB/c bone were stained by flow cytometry. Large cells were then gated and analyzed on a FACScan™ flow cytometer (BDIS, San Jose, CA).
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