Molecular Cloning: A Laboratory Manual, Volume 1 |
From inside the book
Results 1-3 of 64
Page xxv
... 10.40 SUBTRACTED LIBRARIES 10.40 SUBTRACTED PROBES
RADIOLABELED TO HIGH SPECIFIC ACTIVITY 10.43 Synthesis of Total cDNA
Probes Complementary to Single - stranded RNA Using Oligonucleotides as
Primers 10.44 ...
... 10.40 SUBTRACTED LIBRARIES 10.40 SUBTRACTED PROBES
RADIOLABELED TO HIGH SPECIFIC ACTIVITY 10.43 Synthesis of Total cDNA
Probes Complementary to Single - stranded RNA Using Oligonucleotides as
Primers 10.44 ...
Page xxxi
Oligonucleotide - mediated Mutagenesis 15.51 Preparation of Single - stranded
Target DNA 15.53 Design and Selection of Mutagenic Oligonucleotides 15.54
Hybridization of Oligonucleotides to the Template DNA and Primer Extension
15.57 ...
Oligonucleotide - mediated Mutagenesis 15.51 Preparation of Single - stranded
Target DNA 15.53 Design and Selection of Mutagenic Oligonucleotides 15.54
Hybridization of Oligonucleotides to the Template DNA and Primer Extension
15.57 ...
Page 1-35
generation of probes , 14.6–14.8 inverse , for amplification of segments flanking
target sequence , 14.1214.13 methods , 14.18–14.19 mixed oligonucleotide
primed amplification of cDNA , 14.7 precautions to prevent contamination , 14.14
...
generation of probes , 14.6–14.8 inverse , for amplification of segments flanking
target sequence , 14.1214.13 methods , 14.18–14.19 mixed oligonucleotide
primed amplification of cDNA , 14.7 precautions to prevent contamination , 14.14
...
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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