- ¥600
- 上海羽朵生物
- YDS3326
- 2025年07月16日
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- 规格：
1x1mL
| 规格 | l零售价（元） |
| 1x1mL | 600 |
| 1x5mL | 2300 |
| 5x1mL | 2600 |
| 3x1mL+1x5mL | 3800 |
| 5x5mL | 8200 |
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| SalmonellaO-antigens,沙门氏菌O抗原 |
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| Bovinecoronavirus,牛冠状病毒 |
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| IBV,传染性支气管炎病毒 |
| IBDV,传染性法氏囊病毒 |
| H5，甲型流感H5亚型 |
| H7，甲型流感H7 |
| MDV,马立克氏病 |
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文献和实验Coupling Antibodies to Protein A or G
1. use 2 mg of antibody per ml wet beads (use appropriate antibody/protein A or G combination). 2. mix antibodies with beads and bind at room temperature for at least 1 hr (on roller). 3. wash the beads twice with 10 volumes borate buffer, spin
Mouse B cell isolation with magnetic beads
ml conical tube; 6.Centrifuge cells at 1700 rpm(500 g), 5 min, 4°C; 7. Remove red blood cell : Resuspend cells in ACK to 1 ml/1X10 8 cells, and stand in RT for 1 min. Constant volume to 20 ml/ 1X10 8 cells
Purification of DNA Fragments from Agarose Gels Using Glass Beads
to glass surfaces at high salt concentration. A very high DNA binding capacity is achieved by using a fine powder of crushed glass. After washing, the DNA can be readily eluted from the glass in water, at a final concentration of up to 100 �g/mL.
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