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- 文献和实验
- 技术资料
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见瓶身
- 保质期:
/
- 英文名:
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999
- 供应商:
麦飞生物
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- 规格:
15 ml
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文献和实验1) After ECL development, wash membrane once for 10min with PBST. 2) Incubate the membrane in stripping buffer (see below) in a heat-sealed plastic bag for 30min at 50oC with occasional mixing. For low-abundance antigens, the strip
RNA-chromatin immunoprecipitations (RNA-ChIP) in mammalian cells
. Washes Each immune complex was washed five times (1 ml wash, 5 minutes each). After each wash, complexes were pelleted by gentle centrifugation (1000 rpm, 1 minute) and the wash buffer aspirated using a clean pipet tip: Low-salt wash
Synthesis and Probing of Membrane-bound Peptide Arrays
. MATERIALS Buffers, Solutions, and Reagents Buffer salts and ingredients should be of biochemical grade. Bromophenol blue indicator (BPB), 10 mg per ml
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