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| 357501 | PIPETASPIRATING5ML | 200 |
| 357506 | PIPETSEROL1MLBY1/100MLINCRBP25/box1000/cs | 1000 |
| 357507 | PIPETSEROL2MLBY1/100MLINCR 100/box1000/cs | 1000 |
| 357508 | PIPETSEROL2MLBY1/100MLINCRBP25/box1000/cs | 1000 |
| 357515 | PIPETSEROL25MLBY1/4MLINCRBP20/box200/cs | 200 |
| 357521 | PIPETSEROL1MLBY1/100MLINCR 100/box200/cs | 1000 |
| 357524 | PIPETTRANSFER6INCHNONSTERILE 1000CS | 1000 |
| 357525 | PIPETSEROL25MLIN1/4MLINCR50/box200/cs | 200 |
| 357529 | PIPETSEROL5MLBY1/10MLINCR25/Box500/cs | 500 |
| 357530 | PIPETSEROL10MLBY1/10MLINCR25/BP500/cs | 500 |
| 357535 | 200/cs | 200 |
| 357543 | PIPETSEROL5MLBY1/10MLINCR50/box200/cs | 200 |
| 357550 | PIPETSEROL50MLBY1ML INCR25/box100/cs | 100 |
| 357551 | PIPETSEROL10MLBY1/10MLINCR50/box200/cs | 200 |
| 357558 | PIPETASPIRATING2ML | 200 |
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文献和实验SQ Blood DNA Maxi Protocol for 4-10 ml whole blood
15 ml microcentrifuge tubes 3. Water baths preset at 37°C 4. Paper towels 实验步骤 1. Add one volume of whole blood (or bone marrow) to a nuclease-free 50 ml centrifuge tube containing 3 volume of Buffer ERL. Mix
Immunoprecipitation and Immune Complex kinase assay--according to Tamara Hurley
bucket centrifuge, resuspend in approximately 1 ml Tris and spin at 2K in a microfuge. Wash on plate if adherent cells by aspirating medium, adding 2 to 10 ml Tris, and aspirating again. 2) Lyse cells at 107 cells/ml or (minimally) 500
Freeze-Crack P granule Staining Protocol
Freeze-Crack P granule Staining Protocol 1. Prepare humidity chamber: line large square plate with humid paper towels and place 4 5ml plastic pipets across chamber to support slides. Place aluminum block in dry ice
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