Molecular Cloning: A Laboratory Manual, Book 3 |
From inside the book
Results 1-3 of 22
Page xxii
24 Purification and Ligation of the Target DNA 13 . 24 Fragmentation of the
Target DNA 13 . 26 SONICATION 13 . 26 DIGESTION WITH DNAase I IN THE
PRESENCE OF MANGANESE IONS 13 . 28 Repair and Size Selection of DNA
13 .
24 Purification and Ligation of the Target DNA 13 . 24 Fragmentation of the
Target DNA 13 . 26 SONICATION 13 . 26 DIGESTION WITH DNAase I IN THE
PRESENCE OF MANGANESE IONS 13 . 28 Repair and Size Selection of DNA
13 .
Page xxiv
15 Tag DNA POLYMERASE 14 . 16 DEOXYRIBONUCLEOSIDE
TRIPHOSPHATES 14 . 16 TARGET SEQUENCES 14 . 16 Amplification
Reactions 14 . 18 Amplification of DNA Generated by Reverse Transcription of
mRNA 14 .
15 Tag DNA POLYMERASE 14 . 16 DEOXYRIBONUCLEOSIDE
TRIPHOSPHATES 14 . 16 TARGET SEQUENCES 14 . 16 Amplification
Reactions 14 . 18 Amplification of DNA Generated by Reverse Transcription of
mRNA 14 .
Page 1
The target fragment can then be ligated to the vector without enzymatic
manipulation of either piece of DNA . In many cases , however , the termini of the
target fragment and vector are incompatible . It is then necessary to convert one
or both ...
The target fragment can then be ligated to the vector without enzymatic
manipulation of either piece of DNA . In many cases , however , the termini of the
target fragment and vector are incompatible . It is then necessary to convert one
or both ...
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LibraryThing Review
User Review - iayork - LibraryThingthe BIBLE of every biologist: So few and so much to say about this bible of Biology at the bench... You'll really find everything you want in it, including the composition of all the buffers and ... Read full review
Contents
BOOK | 3 |
Identification and Analysis of Recombinants 2 108 | 30 |
TRANSFECTION MEDIATED BY DEAEDEXTRAN 16 | 41 |
Copyright | |
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Common terms and phrases
acetate activity added Adjust aliquots allow amount antibody antigen Appendix appropriate approximately aqueous assay bacterial bacteriophage base binding buffer carried cells centrifugation Chapter chromatography Cl pH cloned coli column complete concentration containing culture deionized water described desired detected dilution Dissolve EDTA efficiency electrophoresis enzyme et al ethanol expression extract Figure filter final fragment gene growth hybridization Incubate levels ligation mammalian cells medium method mg/ml microfuge tube minutes mixture mRNAs nucleic acid pellet phase phosphate Place plasmid plate polymerase precipitation prepared procedure Products promoter protein radioactive radiolabeled reaction remove restriction room temperature sample screen selection sequence sodium solution specific step sterile stored strain TABLE Telephone termini tion transcription transfection transfer transformation Tris ug/ml usually vectors volume wash western blotting ОН