CD45+ T cells were enriched from or removed from a mixed population of splenocytes from C57BL/6 mice and Jurkat cells (human T-cell leukemia T lymphocytes). Subsequently,fluorescent staining was performed using anti-CD45 (clone: 30-F11) Alexa Fluor™ 488, and the live cell population was gated for analysis.
Product Details
Product Details
Product Specification
| Format | Dextran-coated iron tetroxide magnetic nanoparticles conjugated with an anti-mouse CD45 monoclonal antibody |
| Capacity |
2 mL magnetic beads: suitable for a total cell count of 1×10⁹, and can perform up to 100 separations 1 mL magnetic beads: suitable for 5×108total cells, and can perform up to 50 separations |
| Principle of Separation | CD45⁺ cells are magnetically labeled using CD45 Nanobeads for mice. The cell suspension is then loaded into a separation column placed within the sorter's magnetic field. The magnetically labeled CD45⁺ cells remain retained in the column, while the unlabeled cells elute; this fraction constitutes the negative fraction after removal of CD45⁺ cells. After removing the separation column from the magnetic field, the magnetically captured CD45⁺ cells can be eluted, yielding the positive sorted fraction. If higher purity is required, the positive fraction containing CD45⁺ cells must be further separated through a second separation column. |
| Reactivity | Mouse |
| Magnetic Bead Size | 20 nm |
| Separation Method | Column-Based |
| Selection Strategy | Positive Selection |
| Stability & Storage | Store protected from light at 2–8°C; do not freeze. |
Background
CD45 Nanobeads, mouseUsed for positive selection or depletion of leukocytes from both lymphoid and non-lymphoid tissues. The CD45 antigen is expressed on all hematopoietically derived cells, except for red blood cells and platelets.
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Validation Data

