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Catalog Number | orb44197 |
---|---|
Category | Antibodies |
Description | Mouse Monoclonal to CD222. |
Clonality | Monoclonal |
Clone Number | MEM-238 |
Tested applications | FC, IP, WB |
Reactivity | Human, Primate |
Isotype | Mouse IgG1 |
Immunogen | Recombinant Vaccinia virus encoding CD222. |
Antibody Type | Primary Antibody |
Concentration | 1 mg/ml |
Dilution range | Flow cytometry: Extracellular and intracellular staining. Recommended dilution: 2-6 μg/ml. Western blotting: Non-reducing conditions. |
Purity | Purified by protein-A affinity chromatography. |
Conjugation | Unconjugated |
Target | CD222 |
Entrez | 3482 |
UniProt ID | P11717 |
RRID | AB_10993907 |
Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Buffer/Preservatives | Phosphate buffered saline (PBS), pH 7.4, 15 mM sodium azide |
Alternative names | Anti-CD222 antibody, anti-IGF2 receptor antibody, Read more... |
Note | For research use only |
Application notes | Flow cytometry: Extracellular and intracellular staining. Recommended dilution: 2-6 μg/ml. Western blotting: Non-reducing conditions. Recommended dilution: 1-2 µg/ml. |
Expiration Date | 12 months from date of receipt. |
Separation of human neutrophil granulocytes (red-filled) from lymphocytes (black-dashed) in flow cytometry analysis (surface staining) of human peripheral whole blood stained using anti-human CD222 (MEM-238) purified antibody (concentration in sample 2 µg/ml) GAM APC.
Flow cytometry surface staining pattern of human peripheral whole blood stained using anti-human CD222 (MEM-238) purified antibody (concentration in sample 2 µg/ml) GAM APC.
Anti-Hu CD222 Purified (clone MEM-238) works in WB application under non-reducing conditions. Western blotting analysis was performed on whole cell extracts (RIPA lysis buffer) of Jurkat, K562, Raji, and HeLa cell lines, mixed and heated (100°C, 5 min) with reducing and non-reducing SDS-loading buffer. Samples were resolved using 7% Tris-glycine SDS gel electrophoresis. Nitrocellulose membrane blot was probed with mouse IgG1 monoclonal antibody MEM-238 (1 µg/ml), followed by IRDye 800CW Goat-anti-Mouse IgG (green). Mouse anti-GAPDH monoclonal antibody FF26A conjugated with DyLight 680 (0.1 µg/ml), was used as the loading control (red). Multiplex fluorescent Western blot detection was performed. CD222 molecules were detected at ~250 kDa in all analysed cell lines.