Molecular Cloning: A Laboratory Manual, Volume 1 |
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Page 163
If the concentration of DNA in the reaction is low , the chances are good that
these two termini will belong to the same molecule of DNA ... Thus , at low
concentrations of DNA , recircularization of the plasmid DNA will occur with high
efficiency .
If the concentration of DNA in the reaction is low , the chances are good that
these two termini will belong to the same molecule of DNA ... Thus , at low
concentrations of DNA , recircularization of the plasmid DNA will occur with high
efficiency .
Page 164
For doublestranded DNA with self - complementary cohesive termini , i = 2 N M x
10-3 ends / ml where N. is Avogadro's number and M is the molar concentration
of the DNA . Theoretically , when j = i , the end of a given DNA molecule is ...
For doublestranded DNA with self - complementary cohesive termini , i = 2 N M x
10-3 ends / ml where N. is Avogadro's number and M is the molar concentration
of the DNA . Theoretically , when j = i , the end of a given DNA molecule is ...
Page 7-8
Add MgCl , and dithiothreitol to final concentrations of 10 mm and 0.1 mm ,
respectively , and then add placental RNAase inhibitor or vanadylribonucleoside
complexes to a final concentration of 1000 units / ml or 10 mm , respectively . 7.
Add MgCl , and dithiothreitol to final concentrations of 10 mm and 0.1 mm ,
respectively , and then add placental RNAase inhibitor or vanadylribonucleoside
complexes to a final concentration of 1000 units / ml or 10 mm , respectively . 7.
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Common terms and phrases
activity agar agarose aliquots allow amount appropriate arms bacterial bacteriophage BamHI buffer carrying cells centrifugation Chapter cloning coli colonies completely concentration construction containing cosmid culture described digestion EcoRI efficiency electrophoresis et al ethanol ethidium ethidium bromide extracts Figure filters final foreign DNA fragments gene genetic genome growth Hindi host hybridization Incubate infected inserted libraries ligase ligation linear method microfuge minutes minutes at 4°C mixture molecules mutations nucleic acids obtained original packaging particles pellet plaques plasmid DNA plate polycloning polymerase possible precipitate prepared presence probes problem procedure promoter protein purified reaction recombinant Recover region remove replication restriction enzyme room temperature Sall segment selection sequences single single-stranded Smal solution step sterile stored strains strand supernatant termini transfer transformation tube usually vector volume Xbal yield