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Your present location:HomeProductsCloning and Mutagenesis SystemCloning Competent Cells / Trans1-Blue Chemically Competent Cell
  • Product Name: Trans1-Blue Chemically Competent Cell
  • Catalog Number: CD401
  • Storage: at -70 °C for six months
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Overview

Description

Trans1-Blue Chemically Competent Cell is specifically designed for chemical transformation of DNA. It permits a transformation efficiency of over 108 cfu/μg DNA (tested by pUC19 plasmid DNA). The competent cell is resistant to tetracycline (TetR).

 

Genotype

recA1 endA1 gyrA96 thi-1 hsdR17 supE44 (rk-,mk+), relA1 lac [F' proAB lacIqZΔM15: Tn10 (TetR)]

 

Features

• High transformation efficiency: >108 cfu/μg ( pUC19 DNA).

• TetR.

• Blue/white selection.

 

Procedures

•Equilibrate a water bath to 42oC.

•Warm a vial of SOC medium or LB medium to room temperature. Warm selective plates at 37oC for 30 minutes.

•Thaw a vial of 100 μl of Trans1-Blue Chemically Competent Cell on ice, aliquot 50 μl of the cells into a prechilled 1.5 ml tube, add target DNA (1 to 5 μl ) into the tube. Do not mix by pipetting up and down. Incubate the cells on ice for 30 minutes.

•Heat-shock the cells for 45 seconds at 42oC without shaking. Immediately transfer the tube to ice. Incubate on ice for 2 minutes without shaking.

•Add 500 μl of prewarmed SOC medium or LB medium (without antibiotic) into the tube, mix well and shake at 37oC for 1 hour at 200 rpm for cell recovery and for the expression of antibiotic resistance.

•Spread 20 to 200 μl from each transformation vial on a prewarmed selective plate. The remaining can be stored at 4oC and plated the next day if needed.

•Invert the plate and incubate at 37oC overnight.

•Select colonies and analyze by restriction enzyme digestion, PCR, or sequencing.

 

Notes

•Higher efficiency transformation can be achieved by transforming cells immediately following thawing.

•Avoid repeated thawing.

•Gentle handling is required for the entire procedure.

 

Contents& storage

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Citations & references
Literature Journal IF Author Date Link
Role of two amino acid residues’ insertion on thermal stability of thermophilic α-amylase AMY121 from a deep sea bacterium Bacillus sp. SCSIO 15121 Bioprocess and Biosystems Engineering 1.997 Lizhen Li, et al. 2015 May http://link.springer.com/article/10.1007/s00449-014-1330-2
The N-Terminal GH10 Domain of a Multimodular Protein from Caldicellulosiruptor bescii Is a Versatile Xylanase/β-Glucanase That Can Degrade Crystalline Cellulose Applied and Environmental Microbiology 3.668 Xianli Xue, et al. 2015 Mar http://aem.asm.org/content/81/11/3823.short
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