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- 文献和实验
- 技术资料
- 保存条件:
低温
- 保质期:
保质期内
- 英文名:
MKM
- 库存:
充足
- 供应商:
北京美科美生物技术开发有限公司
- CAS号:
来电咨询
- 规格:
1 ml
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文献和实验Purification of DNA‐Binding Proteins Using Biotin/Streptavidin Affinity Systems
of DNA?either natural or formed from oligonucleotides?containing a high?affinity site for a DNA?binding protein provide a powerful tool for purification. The biotin/streptavidin purification system is based on the tight and essentially irreversible
DNA Isolation from Agarose Gels with DEAE Paper
as supplied by Schleicher and Schuell, however the binding capacity can be increased by washing the paper in 10mM EDTA, pH 7.5 for 10 minutes, 0.5M NaOH for 5 minutes, followed by several rinses in distilled water. The paper can be stored at 4o C
Purification of DNA Fragments from Agarose Gels Using Glass Beads
agarose, electrophoresis onto DEAE-cellulose paper, electroelution (with many variations), and usage of various DNA binding matrices. The following method is based on the capacity of sodium iodide (NaI) to dissolve agarose gels and the binding of DNA
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