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- 文献和实验
- 技术资料
- 保存条件:
低温
- 英文名:
11814427001
- 库存:
现货
- 供应商:
上海善然生物科技有限公司
ApplicationReady-to-use, disposable, microfuge-compatible columns designed for the removal of unincorporated radiolabeled nucleotides from RNA labeled by polymerase or end-labeling techniques.[1][2][3]
Use the highly purified RNA in northern blotting.
The mini Quick Spin columns are designed for use with variable-speed, fixed-angle microcentrifuges.Features and Benefits• Save time and effort with ready-to-use columns.
• Purify more nucleic acid in less time - process up to 75μl of sample in only 7 minutes.
• Minimize sample loss while maximizing yield - short and effective two-step procedure.
• Easy-to-use - column and cap allow for rapid resuspension of the gel matrix, and the bottom tip can be quickly snapped off.
• Ensure optimal performance and reproducibility with quality tested columns:
High recovery of radiolabeled RNA
Maximum retention of unincorporated nucleotides
Absence of RNases
Contents
Pre-packed, pre-swollen, microfuge-compatible columns with a cap and snap-off bottom tip.
Suspension of Sephadex G-50 in STE buffer (10mM Tris-HCI, pH 7.5, 1mM EDTA, 100mM NaCl).General description下载特定产品批次和规格的CofA、SDS和IFU。 Ready-to-use, microcentrifuge-compatible chromatography columns for quick and efficient purification of RNA from labeling reactions.Other Notes仅用于生命科学研究。不可用于诊断。PrincipleThe mini Quick Spin gel filtration columns separate molecules based on their relative size. This rapid chromatographic separation can be done in a conventional tabletop microcentrifuge. During centrifugation, mini Quick Spin Columns allow larger molecules (DNA, RNA, or oligonucleotides) to pass through quickly while retaining smaller molecules, such as unincorporated nucleotides.Preparation NoteSample size: 20 – 75μl
Time required: 7 minutes
Reactions/standard sample: 50QualityRNases are not detected, according to the current Quality Control procedures.SpecificationsRecovery of labeled RNA: ≥80%
Retention of unincorporated nucleotides: >99%
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文献和实验秒。在4℃下以12,000g离心裂解物20分钟并收集上清液。用600μl缓冲液NPI-10平衡Ni-NTA离心柱,以890g离心2分钟。将含有6×His标记蛋白的600-μl裂解液加载到预平衡的Ni-NTA离心柱上,以270 g离心5分钟并收集流通液用600μl缓冲液NPI-20洗涤Ni-NTA离心柱三次,以890g离心2分钟。用300μl缓冲液NPI-500洗脱蛋白质两次,以890g离心2分钟并收集洗脱液。经验如果缓冲液中的固体颗粒阻塞旋转柱,则应首先过滤该方案中使用的所有缓冲液,并确保缓冲液含有精确
至1.10–1.13。填料体积偏差对BXP层析柱柱高影响较大,如果需要严格按照压缩系数装填,可以先用30-60cm/h流速进行沉降。下压操作也可根据经验进行:在采用本文推荐的装柱缓冲液和流速装柱的场景下,20 cm左右的标记高度,可下压到标记高度以下1-1.5 cm的形式完成压柱。 其他 BXP层析柱整体装柱流程与BXK系列基本一致,本文重点介绍的是两者在结构设计及装柱细节上的区别。 如果您希望系统了解实验室层析柱的完整装柱流程,可参考过往推文《如何快速成为博格隆 BXK 柱装柱达人?》。
11、将树脂/DNA 混合液抽干后,加13ml柱子洗脱溶液至离心管中, 对管底部的树脂/DNA 进行洗脱(柱子一边旋转一边加入洗脱液),并加入柱子中。 12、真空抽干所加入的洗脱。 13、 再加12ml柱子洗脱液进柱子并抽干。 14、 加入5ml 80%乙醇漂洗柱中的树脂, 柱子真空抽干后将柱子放入用户提供的离心管中,2500rpm(1300g)离心5分钟。 15、 取出柱子,真空抽干5分钟,再将柱子放入系统中所提供的离心管中,2500rpm(1300g)离心5分钟。 16
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