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Sigma-Aldrich

GenElute 哺乳动物基因组DNA小量制备试剂盒

sufficient for 10 purifications

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别名:
哺乳动物基因组DNA小量制备, Gen Elute
NACRES:
NA.55

用途

sufficient for 10 purifications

储存温度

15-25°C

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一般描述

GenElute哺乳动物基因组DNA纯化试剂盒可以简单、方便地从多种哺乳动物源样本中分离高纯度的大分子量DNA。此类试剂盒使用了为基因组DNA纯化精选的硅胶膜,采用了方便的离心柱形式。

可从培养细胞、组织(包括啮齿动物尾巴)以及新鲜的全血或白血细胞之中分离高纯度的基因组DNA。该试剂盒将硅胶膜技术的优势与微量离心形式结合在一起,同时无需采用昂贵的树脂、乙醇沉淀,以及诸如苯酚和氯仿等有害化学成分。

应用

纯化所得的基因组DNA可直接供以下下游应用使用:
  • 限制性内切酶酶切
  • PCR
  • Southern印迹
  • 测序反应
  • 克隆
  • 连接

特点和优势

  • 预期得率:25 μg / 2 x 106个培养细胞;30 μg / 25 mg组织
  • 洗脱体积:200 - 400 μl
  • 所需时间:细胞裂解后20分钟
  • A260/A280比率:1.6 - 1.9
  • 是否需要机械式均质化:否

原理

起始材料首先使用含有离液盐的溶液进行裂解,以确保大分子彻底变性。之后加入乙醇,裂解物离心通过微量离心管时,DNA会结合到硅胶模上。在洗涤去除污染物后,将DNA放在200 μL的Tris-EDTA溶液中洗脱。预期的基因组DNA得率很大程度上取决于所用的起始材料用量及类型。通过本试剂盒纯化所得的DNA的A260/A280比率介于1.6-1.9之间,最大长度可达50 kb。

其他说明

更多信息,请见www.sigma-aldrich.com/genomicdna

法律信息

GenElute is a trademark of Sigma-Aldrich Co. LLC

试剂盒组分也可单独购买

产品编号
说明
化学品安全说明书

  • C2112Column Preparation Solution化学品安全说明书

  • P2308Proteinase K from Tritirachium album, lyophilized powder, BioUltra, ≥30 units/mg protein, for molecular biology化学品安全说明书

  • R6148RNase A solution化学品安全说明书

推荐

警示用语:

Danger

危险分类

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Met. Corr. 1 - Resp. Sens. 1 - Skin Irrit. 2

储存分类代码

8A - Combustible, corrosive hazardous materials

WGK

WGK 3

闪点(°F)

483.8 °F

闪点(°C)

251 °C

法规信息

常规特殊物品

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Züleyha Doğanyiğit et al.
Phytomedicine : international journal of phytotherapy and phytopharmacology, 20(7), 632-639 (2013-03-05)
In recent years, propolis has been the object of extensive research for its antibacterial, antioxidant, anti-inflammatory, and antitumoral activities. This study aims to determine the hepatoprotective efficiency of propolis on experimental endotoxemia in rats. In the current study, fifty adult
Yuma Yamada et al.
Biomaterials, 33(15), 3952-3958 (2012-03-06)
A quantitative comparison between nuclear DNA release from carriers and their transfection activity would be highly useful for improving the effectiveness of non-viral gene vectors. We previously reported that, for condensed DNA particles, a close relationship exists between the efficiency
Coralie Bertheau et al.
Molecular ecology, 22(12), 3318-3332 (2013-05-29)
Ips typographus and Pityogenes chalcographus are two sympatric Palearctic bark beetle species with wide distribution ranges. As both species are comparable in biology, life history, and habitat, including sharing the same host, Picea abies, they provide excellent models for applying
Matthew J Coussens et al.
Journal of visualized experiments : JoVE, (62)(62), e3303-e3303 (2012-04-18)
The Target ID Library is designed to assist in discovery and identification of microRNA (miRNA) targets. The Target ID Library is a plasmid-based, genome-wide cDNA library cloned into the 3'UTR downstream from the dual-selection fusion protein, thymidine kinase-zeocin (TKzeo). The
Giulia Crispino et al.
Scientific reports, 7(1), 6567-6567 (2017-08-06)
We have previously shown that in vitro transduction with bovine adeno-associated viral (BAAV) vectors restores connexin expression and rescues gap junction coupling in cochlear organotypic cultures from connexin-deficient mice that are models DFNB1 nonsyndromic hearing loss and deafness. The aims

商品

简单的DNA和RNA纯法方法大幅推动了基因组和基因表达的分析和鉴定。人们需要快速、方便地从多种细胞来源分离DNA和RNA,包括哺乳动物、植物和细菌培养物来源的细胞和组织。

The availability of simple methods for purification of DNA and RNA has greatly facilitated the analysis and characterization of the genome and gene expression. There is a demand to isolate DNA and RNA rapidly and conveniently from a variety of cellular sources, including cells and tissues from mammalian, plant and bacterial cultures.

实验方案

Archived Formalin-fixed, Paraffin-embedded (FFPE) tissue samples are invaluable resources for profiling gene expression and studying a variety of diseases.

存档的福尔马林固定和石蜡包埋 (FFPE) 组织样本是分析基因表达和研究多种疾病的宝贵资源。

This protocol provides a simple and convenient method to isolate, amplify, and purify genomic DNA from buccal swabs. Buccal swabs are a convenient method of acquiring a DNA sample.

This protocol provides a simple and convenient method to isolate, amplify, and purify genomic DNA from buccal swabs. Buccal swabs are a convenient method of acquiring a DNA sample.

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相关内容

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