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| Items | Size （2mg） | Size（5mg X 2） |
| Particle size | 2 μm | 2 μm |
| Physical appearance | Powder mixture | Powder mixture |
| Amount of Coupled Protein | ≈1032 pmol (32.6 μg) TROP-2/mg beads | ≈1032 pmol (32.6 μg) TROP-2/mg beads |
| Binding Capacity | >266 pmol (40μg) Anti-trop-2 antibody/mg beads | >266 pmol (40μg) Anti-trop-2 antibody/mg beads |
| Formulation | PBS, pH7.4, with 10% Trehalose | PBS, pH7.4, with 10% Trehalose |
| Reconstitution | 2 mL sterile deionized water (1 mg beads/mL) | 5 mL sterile deionized water (1 mg beads/mL) |
See Certificate of Analysis (CoA) for detailed instruction.
The magnetic beads technology makes use of the easy and efficient collection of beads in magnetic field to facilitate antibody purification in a simple workflow of “bind-wash-elute”. In contrast to common separation techniques, this method does not require columns or centrifugation, and is therefore ideal in high-throughput applications.
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Immobilized 32.6 μg TROP-2/1 mg beads can bind Anti-TROP-2 mAb with an EC50 of 0.8505 μg/mL.
Accelerated stability test. After placing the lyophilized beads at 37°C for 7 days, binding activity between the Human TROP-2-coupled Magnetic Beads (Cat.No. MBS-K028) and anti-trop-2 mAb showed little deviation from the unaccelerated sample (%RSD<10%). Data were measured on day 0, 3, 7 respectively.
Freeze-thaw stability test. After different freeze-thaw cycles, binding activity between the Human TROP-2-coupled Magnetic Beads (Cat.No. MBS-K028) and anti-trop-2 mAb showed little deviation from the unfreeze-thaw sample (%RSD<10%). Three freeze-thaw cycles were performed.
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