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一般說明
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。
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。
應用
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
特點和優勢
- 典型DNA得率:15 μg - 20 μg
- 提供有适用于革兰氏阳性菌和革兰氏阴性菌的实验方案
- 可在2小时内获得优质基因组DNA
- 可纯化出A260/A280 比率介于1.6-1.9之间的DNA
- 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
原則
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。
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
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说明
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訊號詞
Danger
危險分類
Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Met. Corr. 1 - Resp. Sens. 1 - Skin Irrit. 2 - STOT SE 3
標靶器官
Central nervous system, Respiratory system
儲存類別代碼
3 - Flammable liquids
其他客户在看
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K E Eboigbodin et al.
Applied microbiology and biotechnology, 73(3), 669-675 (2006-07-21)
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Chityal Ganesh Kumar et al.
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Eleven biosurfactant producing bacteria were isolated from different petroleum-contaminated soil and sludge samples. Among these 11 isolates, two were identified as promising, as they reduced the surface tension of culture medium to values below 27 mN m(-1) . Besides biosurfactant
Ivan M Mukisa et al.
International journal of food microbiology, 160(1), 1-10 (2012-11-13)
Obushera includes four fermented cereal beverages from Uganda namely: Obutoko, Enturire, Ekitiribita and Obuteire, whose microbial diversity has not hitherto been fully investigated. Knowledge of the microbial diversity and dynamics in these products is crucial for understanding their safety and
实验方案
的GenElute™细菌基因组DNA试剂盒提供了一种从细菌中分离纯基因组DNA的简便方法。
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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