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- 详细信息
- 询价记录
- 文献和实验
- 技术资料
- 供应商:
北京中北林格科技发展有限公司
- 英文名:
TransforMax™ EPI300™ Electrocompetent E. coli
- 库存:
大量
- 保存条件:
-70℃
TransforMax™ EPI300™ Electrocompetent E. coli
TransforMax™ EPI300™ Chemically Competent E. coli
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电话:010-88891086(806)
联系人:康 乐
| TransforMax™ EPI300™ E. coli cells lack the tonA gene and are engineered for use with EPICENTRE's CopyControl™ cDNA, Gene, and PCR Cloning Kit and other CopyControl Cloning Systems* that do not require phage T1-resistant cells. The cells contain an inducible mutant trfA gene whose gene product is required for initiation of replication from the oriV origin of replication, such as that in CopyControl pCC1™ vectors or in clones that are retrofitted with CopyControl capability using the Benefits
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| Figure 1. Copy number of CopyControl™ BAC clones can be induced 10- to 20-fold in TransforMax™ EPI300™ E. coli. The yield of BAC DNA from CopyControl BAC clones of 110-145 kb increased >14-fold following addition of CopyControl Induction Solution. U=uninduced cells; I=induced cells. |
Genotype
F- mcrA Δ(mrr-hsdRMS-mcrBC) Φ80dlacZΔM15 ΔlacX74 recA1 endA1 araD139 Δ(ara, leu)7697 galU galK λ- rpsL (StrR) nupG trfA dhfr
TransforMax EPI300 Electrocompetent E. coli
- Transformation efficiency of >1 x 1010 cfu/µg of pUC19.
TransforMax EPI300 Chemically Competent E. coli
- Transformation efficiency of >5 x 108 cfu/µg of pUC19.
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文献和实验DNA and RNA Ligases (EC 6.5.1.1, EC 6.5.1.2, and EC 6.5.1.3)
Ligases are a class of enzymes that catalyze the joining of nucleic acid molecules by the formation of phosphodiester bonds between their termini (1 ). The nucleic acid substrate to be linked may be DNA or RNA depending on the type of ligase
Deoxyribonuclease I (EC 3.1.21.1) and II (EC 3.1.22.1)
From Chapter 1 on nucleases, we know that the term DNase refers to an enzyme that endonucleolytically cleaves DNA molecules. This chapter deals with those DNases that preferentially catalyze the hydrolysis of double-stranded DNA (ds DNA
DNA Methyltransferases (EC 2.1.1.72 and EC 2.1.1.73)
for one or the other base, and modify at the 6-NH2 of dA (EC 2.1.1.72) or at the N4 or 5-C position of dC (EC 2.1.1.73) depending on the particular enzyme (2 ). The reaction is predominantly irreversible. Enzymes, such as O 6 -methylguanine DNA Mtase, that participate
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