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NA2100

Sigma-Aldrich

GenElute 细菌基因组DNA试剂盒

sufficient for 10 purifications

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别名:
细菌基因组DNA, Gen Elute
NACRES:
NA.55

用途

sufficient for 10 purifications

储存温度

15-25°C

一般描述

GenElute 细菌基因组DNA试剂盒可以简单、方便地从革兰氏阴性菌中分离高纯度基因组DNA。对于大多数革兰氏阳性菌,本试剂盒必须结合选购的溶菌酶 (L4919)来有效裂解较厚的肽聚糖细胞壁。为方便您制备溶菌酶储液,我们提供了一种稀释的革兰氏阳性溶解溶液。

该试剂盒将硅胶膜系统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

纯化所得的细菌基因组DNA可用于以下游应用:
  • 限制性内切酶酶切
  • PCR
  • Southern印迹
  • 克隆

特点和优势

  • 起始材料:不超过1.5 mL培养物
  • 预期得率:至多20 μg
  • 洗脱体积:400 μl
  • 所需时间:70 - 120分钟
  • A260/A280比率:1.6 - 1.9
  • 无需苯酚、氯仿或乙醇沉淀步骤

原理

细菌首先在含有离液盐的溶液之中裂解,以确保大分子彻底变性。之后加入乙醇,从而使DNA在溶解物通过微量离心管在硅胶膜上离心时,结合到膜上。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得率取决于细菌培养物的细胞密度、细菌种属以及所用的菌株。通过GenElute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

  • W0263Wash Solution 1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

警示用语:

Danger

危险分类

Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Met. Corr. 1 - Resp. Sens. 1 - Skin Irrit. 2 - STOT SE 3

靶器官

Central nervous system

储存分类代码

3 - Flammable liquids

WGK

WGK 2

法规信息

危险化学品
常规特殊物品

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Susana Delgado et al.
Microbial ecology, 65(3), 763-772 (2013-02-12)
Stomach mucosa biopsies and gastric juices samples of 12 healthy persons were analysed by culturing in selective- and non-selective-rich media. Microbial DNA from four mucosal samples was also amplified by nested PCR using universal bacterial primers, and the 16S rDNA
Christopher S Barker et al.
American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics, 143(3), 317-323 (2013-03-05)
Our objective was to determine whether components of fixed orthodontic appliances as received from the manufacturers and after exposure to the clinical environment are free from microbial contamination before clinical use. A pilot molecular microbiologic laboratory study was undertaken at
James A Parejko et al.
Applied and environmental microbiology, 79(12), 3887-3891 (2013-04-16)
We investigated the taxonomic placement of phenazine-producing fluorescent Pseudomonas spp. in the Inland Pacific Northwest region of the United States. Five distinct species were identified, two of which were provisionally considered to be new. Agroclimatic zone and soil silt content
Jeung Hee Lee et al.
Applied microbiology and biotechnology, 96(4), 993-1005 (2012-05-31)
Lipase (lip) and lipase-specific foldase (lif) genes of a biodegradable polyhydroxyalkanoate (PHA)-synthesizing Pseudomonas resinovorans NRRL B-2649 were cloned using primers based on consensus sequences, followed by polymerase chain reaction-based genome walking. Sequence analyses showed a putative Lip gene product (314
Lizbeth Sayavedra et al.
Environmental microbiology, 23(6), 3164-3181 (2021-04-21)
Sulfate-reducing bacteria (SRB) are widespread in human guts, yet their expansion has been linked to colonic diseases. We report the isolation, sequencing and physiological characterization of strain QI0027T , a novel SRB species belonging to the class Desulfovibrionia. Metagenomic sequencing

实验方案

GenElute Bacterial Genomic DNA Kit protocol describes a simple and convenient way for the isolation of pure genomic DNA from bacteria.

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