跳转至内容
Merck

G1N10

Sigma-Aldrich

GenElute 哺乳动物基因组DNA小量制备试剂盒

sufficient for 10 purifications

别名:

哺乳动物基因组DNA小量制备, Gen Elute

登录查看公司和协议定价


About This Item

分類程式碼代碼:
41105501
NACRES:
NA.55

用途

sufficient for 10 purifications

品質等級

儲存溫度

15-25°C

正在寻找类似产品? 访问 产品对比指南

相关类别

一般說明

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。

應用

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

特點和優勢

  • 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

原則

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。

其他說明

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

法律資訊

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

訊號詞

Danger

危險分類

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Met. Corr. 1 - Resp. Sens. 1 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

8A - Combustible corrosive hazardous materials

閃點(°F)

483.8 °F

閃點(°C)

251 °C


分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

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
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
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
Michal Kirshner et al.
Journal of molecular neuroscience : MN, 46(3), 554-568 (2011-09-17)
Pronounced neuropathology is a feature of ataxia-telangiectasia (A-T) and Nijmegen breakage syndrome (NBS), which are both genomic instability syndromes. The Nbs1 protein, which is defective in NBS, is a component of the Mre11/RAD50/NBS1 (MRN) complex. This complex plays a major

商品

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

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.

The GenElute Mammalian Genomic DNA Purification Kit Protocol describes the isolation of pure, high molecular weight DNA from a variety of mammalian sources.

An introduction to both Northern and Southern blotting, popular methods for the transfer of macromolecules to membranous support. This article also offers a Southern blot protocol and a northern blot protocol.

相关内容

GenomePlex® Whole Genome Amplification is the method of extracting DNA from the animal sample. GenomePlex® products have been used to amplify genomic DNA from chicken, porcine, bovine, fish, and shrimp source.

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门