万千商家帮你免费找货
0 人在求购买到急需产品
- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
-20
- 保质期:
1年
- 英文名:
Exonuclease VIII, truncated
- 库存:
999
- 供应商:
上海淳麦
- 规格:
1000U/10000U
Exonuclease VIII, truncated, is a genetically engineered active domain of exonuclease VIII from E. coli. Exonuclease VIII, truncated is able to initiate nucleotide removal from the 5´ termini of linear double-stranded DNA in the 5´ to 3´ direction (1). The enzyme does not degrade supercoiled dsDNA and circular ssDNA.
Product Source
An E. coli strain that carries a plasmid with genetic engineering active domain of Exonuclease VIII.
Reagents Supplied
The following reagents are supplied with this product:
| Store at (°C) | Concentration | |
| NEBuffer 4 | -20 | 10X |
Description
Exonuclease VIII, truncated, is a genetically engineered active domain of exonuclease VIII from E. coli. Exonuclease VIII, truncated is able to initiate nucleotide removal from the 5´ termini of linear double-stranded DNA in the 5´ to 3´ direction (1). The enzyme does not degrade supercoiled dsDNA and circular ssDNA.
Product Source
An E. coli strain that carries a plasmid with genetic engineering active domain of Exonuclease VIII.
Reagents Supplied
The following reagents are supplied with this product:
| Store at (°C) | Concentration | |
| NEBuffer 4 | -20 | 10X |
Advantages and Features
Applications
• Degradation of linear dsDNA while maintaining double stranded circular DNA.
Properties and Usage
Unit Definition
One unit is defined as the amount of enzyme required to produce 1 nmol of acid-soluble deoxyribonucleotide from double-stranded DNA in a total reaction volume of 50 µl in 30 minutes at 37°C in 1X NEBuffer 4 with 0.15 mM sonicated duplex [3H] DNA.
Reaction Conditions
1X NEBuffer 4
Incubate at 37°C
1X NEBuffer 4:
50 mM Potassium Acetate
20 mM Tris-acetate
10 mM Magnesium Acetate
1 mM DTT
pH 7.9 @ 25°C
Storage Temperature
-20°C
Storage Conditions
50 mM Tris-HCl
100 mM NaCl
0.1 mM EDTA
1 mM DTT
0.1% Triton® X-100
50% Glycerol
pH 7.5 @ 25°C
Heat Inactivation
70°C for 15 min
Unit Assay Conditions
1X NEBuffer 4 with 0.15 mM with sonicated duplex 3H- DNA.
References
1. Chang, et al. (2001). J. Biol. Chem.. 46004–46010.

上海淳麦生物科技有限公司专注于感受态细胞、质粒、载体、农杆菌、酵母等生命科学领域的产品研发和技术服务支持。
上海淳麦生物科技有限公司在感受态细胞的研发方面,实力雄厚,拥有了克隆、表达、酵母和农杆菌4大类,共计百余种感受态细胞。在电击感受态方面,拥有了大肠杆菌和农杆菌电击感受态种类,极大提高了客户在转基因以及文库构建方面的成功率。

风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验EXAMINING THE FUNCTION OF PROTEINS AND PROTEIN NETWORKS WITH THE YEAST TWO-HYBRID SYSTEM
I. SUMMARY The yeast two-hybrid system provides a relatively straight forward approach to understanding protein function. Section II outlines the basic components of the interaction trap, a yeast two-hybrid
In situ hybridization of yeast cells (RNA and Oligonucleotide probes)
I. General considerations: In situ hybridization of yeast cells is almost identical to mammalian cells, except that the cell wall has to be removed by spheroplasting the cells prior to hybridization. The following
Preparation of Poly A+ RNA and Northern Analysis
Preparation of Poly A+ RNA and Northern Analysis Procedure (Pharmacia #27-9255-01) Use RNase-free tips and reagents and wear gloves 1) Remove organs from six C57Bl mice (do cervical dislocation immediately before organ
技术资料暂无技术资料 索取技术资料





