Molecular Cloning: A Laboratory Manual, Book 2 |
From inside the book
Results 1-3 of 88
Page 42
3o Assll ^ 1 - 2 cits 857 sr114° nin5 sr115° Sam100 Note : For a more detailed
description of agt18 and agt19 , see Chapter 2 , page 2 . 45 . ugt20 , agt21 agt20
and igt21 were derived from Igt18 and agt19 , respectively ( Han and Rutter 1988
) ...
3o Assll ^ 1 - 2 cits 857 sr114° nin5 sr115° Sam100 Note : For a more detailed
description of agt18 and agt19 , see Chapter 2 , page 2 . 45 . ugt20 , agt21 agt20
and igt21 were derived from Igt18 and agt19 , respectively ( Han and Rutter 1988
) ...
Page 28
To establish genomic DNA libraries , ligate the fractionated DNA to cosmid
vectors or to the arms of bacteriophage i vectors as described in Chapters 3 and
2 ... described in Chapter 2 , for bacteriophage 1 , or Chapter 3 , for cosmids .
To establish genomic DNA libraries , ligate the fractionated DNA to cosmid
vectors or to the arms of bacteriophage i vectors as described in Chapters 3 and
2 ... described in Chapter 2 , for bacteriophage 1 , or Chapter 3 , for cosmids .
Page 72
65 ) may be screened with " PP - labeled oligonucleotide probes as described in
detail in Chapter 11 . However , because putative positive colonies almost
certainly contain a mixture of wild - type and mutated molecules , it is necessary
to ...
65 ) may be screened with " PP - labeled oligonucleotide probes as described in
detail in Chapter 11 . However , because putative positive colonies almost
certainly contain a mixture of wild - type and mutated molecules , it is necessary
to ...
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
Contents
TEST LIGATION 3 29 | 3 |
SYNTHESIS OF THE FIRST STRAND OF cDNA 8 | 11 |
FRAGMENT OF E coli DNA POLYMERASE I 13 59 | 14 |
Copyright | |
92 other sections not shown
Other editions - View all
Common terms and phrases
acid activity agarose aliquots allow amount amplification appropriate approximately bacteriophage bacteriophage T4 base buffer carried cDNA cells centrifugation Chapter chromatography cleaved clones colonies concentration constructed containing deletions denatured described determine digestion DNA polymerase dNTPs double-stranded efficiency electrophoresis et al ethanol expression Figure filters fragment gene genomic hybridization increase Incubate inserted interest isolated labeled length libraries ligation linear linkers method microfuge minutes mixture molecules mRNA mutagenesis mutagenic mutations Nucleic nucleotides obtained oligonucleotide original plaques plasmid plasmid DNA plate pool position possible prepared presence primer probe problem protein purified radiolabeled reaction recombinant region remove restriction enzyme room temperature samples screening sequence single single-stranded solution specific step Store strand synthesis target DNA target sequence template termini tion transfer transformants tube units usually vector volume