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HLA-DR1 (empty) Antibody
Description
Images & Validation
−| Tested Applications | ELISA, FC, WB |
|---|---|
| Reactivity | Human |
| Application Notes |
Key Properties
−| Antibody Type | Primary Antibody |
|---|---|
| Clonality | Monoclonal |
| Isotype | Mouse IgG2b |
| Clone No. | MEM-267 |
| Immunogen | Purified, insoluble DR1 beta chain (DRB1*0101) expressed in E. coli inclusion bodies. |
| Target | HLA-DR1 (empty) |
| Purification | Purified by protein-A affinity chromatography. |
| Conjugation | Unconjugated |
Storage & Handling
−| 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 |
| Concentration | 1 mg/ml |
| Disclaimer | For research use only |
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Separation of human HLA-DR1 positive lymphocytes (red-filled) from HLA-DR1 negative lymphocytes (black-dashed) in flow cytometry analysis (surface staining) of peripheral whole blood stained using anti-human HLA-DR1 (empty) (MEM-267) purified antibody (concentration in sample 9 µg/ml, GAM APC).

Flow cytometry surface staining pattern of human peripheral whole blood using anti-human HLA-DR1 (empty) (MEM-267) purified antibody (concentration in sample 9 µg/ml, GAM APC).

Anti-HLA-DR1 (empty) (clone MEM-267) works in WB application under reducing and non-reducing conditions. Western blotting analysis was performed on whole cell extracts (RIPA lysis buffer) of Raji and Jurkat cell lines, mixed and heated (100°C, 5 min) with reducing and non-reducing SDS-loading buffer. Samples were resolved using 10% Tris-glycine SDS gel electrophoresis. Nitrocellulose membrane blot was probed with mouse IgG2b monoclonal antibody MEM-267 (1 µg/ml), followed by IRDye 800CW Goat-anti-Mouse IgG (green). Multiplex fluorescent Western blot detection was performed. HLA-DR1 molecules were detected at ~25 kDa in Raji cell line.
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HLA-DR1 (empty) Antibody (orb44258)
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