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- 详细信息
- 文献和实验
- 技术资料
- 库存:
999
- 供应商:
北京泽平
- 现货状态:
热销品大量现货,其余请咨询
- 保修期:
1年
- 规格:
EA
货号:T_70310226421
中文名称:
英文名称:Kapillarsäule OPTIMA-225 ID: 0,25 mm, Filmdicke: 0,25µm, L=25 m
货期:热销品现货,其他请咨询




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文献和实验In-gel Tryptic Digest for Protein ID by Mass Spectrometry
or silver stained gel.Cut gel band into 1 mm cubes using clean razor blade on a clean glass surface.Transfer to an Eppendorf tube.2.Remove excess water with pipet.Add 25-35 μl acetonitrile to tube to cover gel pieces.Incubate 10 minutes at RT to dehydrate
Single Primer ("Semi-Random") P
in the second cycling regime. If that doesn't work, try changing primers. If problems persist, switch to the long method. Do the following PCR reaction: 15 µL H2O 3 µL 10xM-PCRB 3 µL 4 dNTPs @ 2 mM each 3 µL Po @ 5 µM 3 µL template diluted
Combined 3C-ChIP-Cloning (6C) Assay: A Tool to Unravel Protein-Mediated Genome Architecture
; Fisher BP333) T4 DNA ligase (400 U/µL) TE buffer (pH 8.0) Dilute 10X stock to 1X before use. Triton X-100 (20% v/v; VWR) Trypsin (1X; Invitrogen 25300) Equipment Aluminum foil Cell scraper Centrifuge
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