Trans1-T1 Phage Resistant Competent Cell (fast growth) – CD501
174.00$ – 318.00$ CAD
Trans1-T1 Phage Chemically Competent Cell (fast growth)
Trans1-T1 Phage Resistant Chemically Competent cells are specifically designed for chemical transformation of DNA. They are the fastest growing chemically competent cells currently available, offering a doubling time of approximately 50 minutes. Trans1-T1 colonies are visible within 8 hours of plating, enabling you to plate and pick colonies the same day. Perform minipreps after only 4-8 hours of growth from an overnight colony – These cells can save you an entire day of work!
Characteristics of Trans1-T1 Phage Resistant Competent Cells
- Minimal non-specific recombination in your cloned DNA plasmid (recA-).
- Clean preparations of DNA and better results due to the elimination of Endonuclease I (endA1).
- Fast-growth, colonies are visible in 8~9 hours.
- Resistance to T1 and T5 phage (tonA).
- Efficient transformation of unmethylated DNA from PCR amplifications.
- High transformation efficiency: > 10ˆ9 cfu/μg (pUC19 DNA).
- Blue/white selection.
Genotype of MACH1-T1® and Trans1-T1 E.Coli Competent Cells
F- φ80(lacZ)ΔM15 ΔlacX74 hsdR(rK-, mK+) ΔrecA1398 endA1 tonA
Cloning Competent Cell comparison and selection chartCompare !
Product Manual and Datasheet:
Genotype definitions (if applicable to this product)
|ara-14||Blocks arabinose catabolism|
|argF||Ornithine carbamoyltransferase mutation blocks ability to use arginine|
|dam/dcm||Abolishes endogenous adenine methylation at GATC sequences (dam) or cytosine methylation at CCWGG sequences (dcm). Used to propagate DNA for cleavage with certain restriction enzymes (e.g. Ava II, Bcl I)|
|DE3||Lysogen that encodes T7 RNA polymerase. Used to induce expression in T7-driven expression systems|
|endA||endA Mutation in the non-specific endonuclease Endonuclease I; eliminates non-specific endonuclease activity, resulting in improved plasmid preps|
|F´||A self-transmissible, low-copy plasmid used for the generation of single-stranded DNA when infected with M13 phage; may contain a resistance marker to allow maintenance and will often carry the lacI and lacZ∆M15 genotypes|
|galK||Galactokinase mutation blocks catabolism of galactose—cells that are galK minus grow in the presence of galactose as the sole carbon source|
|galU||Glucose-1-phosphate uridylyltransferase mutation blocks ability to use galactose—cells that are galU minus can grow on media that contains galactose as the sole carbon source|
|gyrA96||DNA gyrase mutant produces resistance to nalidixic acid|
|hsd||Mutations in the system of methylation and restriction that allow E. coli to recognize DNA as foreign. The hsd genotype allows efficient transformation of DNA generated from PCR reactions *hsdR–eliminates restriction of unmethylated EcoK I sites. (1) **hs|
|lacI||Encodes the lac repressor that controls expression from promoters that carry the lac operator; IPTG binds the lac repressor and derepresses the promoter; often used when performing blue/white screening or to control expression of recombinant genes|
|lacY1||Blocks use of lactose via β-D-galactosidase mutant|
|lacZ||β-D-galactosidase gene; mutations yield colorless (vs. blue) colonies in the presence of X-gal|
|lacZ∆M15||Element required for β-galactosidase complementation when plated on X-gal; used in blue/white screening of recombinants; usually carried on the lambdoid prophage φ80 or F´|
|leuB||Requires leucine for growth on minimal media via β-isopropyl malate dehydrogenase mutation|
|lon||lon Deficiency in the Lon ATPase-dependent protease; decreases the degradation of recombinant proteins; all B strains carry this mutation|
|mcrA, mcrBC,or mrr||Mutations that allow methylated DNA to not be recognized as foreign; this genotype is necessary when cloning genomic DNA or methylated cDNA|
|nupG||Mutation for the transport of nucleosides|
|ompT||Indicates that the E. coli lack an outer membrane protease—reduces degradation of heterologous the strains and recovery of intact recombinant proteins is improved in ompT minus strains|
|P3||A 60-kb low-copy plasmid that carries the ampicillin and tetracycline resistance genes with amber mutations; used predominantly for selection of supF-containing plasmids; carries the kanamycin resistance gene for selection|
|pLys||pLys Plasmid that encodes T7 lysozyme; used to reduce basal expression in T7-driven expression systems by inhibiting basal levels of T7 RNA polymerase|
|proAB||proAB Requires proline for growth on minimal media|
|recA||Mutation in a gene responsible for general recombination of DNA; particularly desirable when cloning genes with direct repeats|
|relA||RNA is synthesized in absence of protein synthesis (relaxed phenotype) relA locus regulates the coupling between transcription and translation. In the wild type, limiting amino acid concentrations results in the shutdown of RNA synthesis.|
|rpsL||Confers resistance to streptomycin (this makes a mutant ribosomal protein, small subunit, the target of the drug)|
|supE,F||tRNA glutamine suppressor of amber (supE)(UAG) or tyrosine (supF)|
|thi-1||Requires thiamine for growth on minimal media|
|Tn10||Confers tetracycline resistance via a transposon|
|tonA||Confers resistance to the lytic bacteriophage T1, T5 and f80|
|traD, D36||Prevents transfer of F’ episome via transfer factor mutation|
|tsx||Confers resistance to phage T6 and colicin K|
|xyl-5||Blocks catabolism of xylose|
5 x 100 ul, 10 x 100 ul, 20 x 100 ul