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- 2025年07月11日
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999
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北京泽平
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货号：T_70119-156-548
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英文名称：CLEAN ROOM/ISO 7/20X24
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文献和实验Replication timing by density transfer
Calbiochem's Pronase (catalog #53702), which seems pretty clean--i.e., plates spread after Pronase treatment aren't contaminated--but I heard from someone who'd used Sigma's Pronase and had massive growth of Streptomyces. 20x SCP = 0.6 M Na2 HPO
In Situ Hybridization Using Digoxigenin Labeled Probes
morphology. After the pretreatment the slides should be hybridized within 24 hours. 1) Place the slides in 2X SSC at 65°C for 30 minutes 2) Wash for 2 minutes in 2X SSC at room temperature. 3) Acetylate the slides as follows: Prepare 500 ml of 0.1 M
Plant DNA methylation analysis by bisulfite genomic sequencing
) at temperature appropriate for used restriction enzyme; Add 0.5ml Tris-buffer-saturated phenol-chroroform, vortex; Centrifuge with Eppendorf 5414 or equivalent at 10000 x g for 2 minutes; Transfer the upper aqueous phase to clean 1.5ml
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