Molecular Cloning: A Laboratory Manual, Book 2 |
From inside the book
Results 1-3 of 27
Page xxiv
28 QUANTITATION OF INITIAL CONCENTRATION OF TARGET SEQUENCES
14 . 30 References 14 . 34 15 Site - directed Mutagenesis of Cloned DNA
Generation of Deletions and Insertions 15 . 3 SIMPLE DELETIONS OR
INSERTIONS 15 .
28 QUANTITATION OF INITIAL CONCENTRATION OF TARGET SEQUENCES
14 . 30 References 14 . 34 15 Site - directed Mutagenesis of Cloned DNA
Generation of Deletions and Insertions 15 . 3 SIMPLE DELETIONS OR
INSERTIONS 15 .
Page 13-38
This means that it is possible to isolate not only nested deletions , but also groups
of deletions whose endpoints are tightly clustered . ( 2 ) The method is not
restricted to any particular vector . ( 3 ) The entire series of enzymatic reactions ...
This means that it is possible to isolate not only nested deletions , but also groups
of deletions whose endpoints are tightly clustered . ( 2 ) The method is not
restricted to any particular vector . ( 3 ) The entire series of enzymatic reactions ...
Page 15-18
This means that it is possible to isolate not only nested deletions , but also groups
of deletions whose endpoints are tightly clustered . • The entire series of
enzymatic reactions ( exonuclease digestion , treatment with nuclease Si or
mung ...
This means that it is possible to isolate not only nested deletions , but also groups
of deletions whose endpoints are tightly clustered . • The entire series of
enzymatic reactions ( exonuclease digestion , treatment with nuclease Si or
mung ...
What people are saying - Write a review
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
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
Other editions - View all
Common terms and phrases
activity addition aliquots allow amount amplification appropriate approximately bacteriophage bacteriophage T4 base buffer carried cDNA cells centrifugation Chapter chromatography cleavage cleaved clones complete concentration constructed containing deletions denatured described determine digestion dNTPs double-stranded efficiency electrophoresis et al ethanol expression extraction Figure filter four fragment gene genomic DNA hybridization increase Incubate inserted interest isolation Klenow labeled length libraries ligation linear linkers membrane method minutes mixture molecules mRNA mutations nucleic acids nucleotides obtained oligonucleotide original plasmid DNA plate position possible precipitation prepared presence primer probe problem protein purified radioactivity radiolabeled reaction recombinant region remove restriction enzyme room temperature samples screening separate sequence single single-stranded solution specific step stored strand synthesis target DNA target sequence template termini transfer Tris tube units usually vector volume