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- 规格:
1x1mL
| 规格 | l零售价(元) |
| 1x1mL | 1340 |
| 1x5mL | 4760 |
| 5x1mL | 5140 |
| 3x1mL+1x5mL | 7920 |
| 5x5mL | 17500 |
| 沙拉沙星-BSA(或OVA)抗原 |
| 恩诺沙星-BSA(或OVA)抗原 |
| 环丙沙星-BSA(或OVA)抗原 |
| 氧氟沙星-BSA(或OVA)抗原 |
| 氯霉素(CAP)单克隆抗体 |
| 氯霉素(CAP)-BSA(或OVA)抗原 |
| 抗青霉素受体单抗 |
| 头孢氨苄-BSA(或OVA)抗原 |
| 氨苄青霉素-BSA抗原 |
| 氯丙嗪单抗 |
| 西马特罗单抗 |
| 赛庚啶单克隆抗体 |
| 莱克多巴胺(RAC)单抗 |
| 克伦特罗(CL)单抗 |
| 沙丁胺醇(SAL)单抗 |
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文献和实验PREPARATION OF PROTEIN A SEPHAROSE CL 4B BEADS
so that the total volume of beads plus buffer is 2 ml).Blocking and Use1.Remove desired volume of 50% slurry (30 µl of slurry per I.P.or Chip).Put in 15 ml conical tube.2.Spin in table top3.Resuspend beads in cold blocking buffer:T. E.25 ml of T.E0.1% Azide25 µl
Mouse B cell isolation with magnetic beads
and incubate on ice for 15min; l Negative : 1.Resuspend cells with MACS to 400 ul and 80 ul B cell Biotin each spleen,incubate on ice for 15 min; 2. Add 300 MACS and 200 anti-biotin Beads each spleen, incubate on ice for 15 min.
Purification of recombinant sBRF M166L
, prepare the Ni-NTA resin for BRF binding. Transfer 12 mls of Ni-NTA affinity bead slurry (50% beads; 6 ml of beads total) to a 50ml conical tube and centrifuge 3min at 3K RPM in the GPR centrifuge. Equilibrate the beads 2X with Lysis buffer
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