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coli 16S rDNA Contamination 100 U <10 copies Endonuclease 100 U <10% converted Storage -20&°C
The best value available anywhere for simple cloning and plasmid propagation
The QuickExtract Plant method allows for the inexpensive processing of one to hundreds of samples simultaneously
non-catalytic thermostable ligase that catalyzes the intramolecular ligation (i
circularization) of ssDNA templates
E. cloni-10G ELITE Electrocompetent Cells (SOLOs) size:12 rxns coli 16S rDNA Contamination 100E. cloni 10G and 10GF' Electrocompetent Cells Direct replacements for standard cloning strains (e. g., DH5, DH10B, JM109, TOP10, XL1 Blue, etc.) Optimized genetics for high yields: phage T1 resistant, endonuclease and recombination minus, blue white screening capable. Available in a range of high transformation efficiencies (5 109 to 4 1010 cfu g). Convenient packaging options. Lucigens E. cloni competent cells share the most useful genetic elements
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