Molecular Cloning: A Laboratory Manual, Volume 1 |
From inside the book
Results 1-3 of 78
Page 159
Alternatively , the fragment can be inserted into the vector at any sites that
generate compatible termini . For example , the restriction enzymes BamHI and
BglII , which recognize different hexanucleotide sequences , generate restriction
...
Alternatively , the fragment can be inserted into the vector at any sites that
generate compatible termini . For example , the restriction enzymes BamHI and
BglII , which recognize different hexanucleotide sequences , generate restriction
...
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 5-11
NNNNNNC Cp GGNNNNNN5 ' Blunt ends generated in this manner can be
joined using bacteriophage T4 DNA ligase , although the efficiency of the
reaction is somewhat lower than for ligation of cohesive termini . Nevertheless ,
joining of ...
NNNNNNC Cp GGNNNNNN5 ' Blunt ends generated in this manner can be
joined using bacteriophage T4 DNA ligase , although the efficiency of the
reaction is somewhat lower than for ligation of cohesive termini . Nevertheless ,
joining of ...
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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