Molecular Cloning: A Laboratory Manual, Book 2 |
From inside the book
Results 1-3 of 83
Page 92
( 1978 ) devised a strategy to generate and clone large numbers of random
fragments of mammalian genomic DNA . Before then , genomic libraries
consisted of fragments of DNA obtained by complete digestion of genomic DNA
with a ...
( 1978 ) devised a strategy to generate and clone large numbers of random
fragments of mammalian genomic DNA . Before then , genomic libraries
consisted of fragments of DNA obtained by complete digestion of genomic DNA
with a ...
Page 34
TRANSFER OF DNA FROM AGAROSE GELS TO SOLID SUPPORTS There are
three methods to transfer fragments of DNA from agarose gels to solid supports (
nitrocellulose filters or nylon membranes ) : 1 . Capillary transfer . In the capillary
...
TRANSFER OF DNA FROM AGAROSE GELS TO SOLID SUPPORTS There are
three methods to transfer fragments of DNA from agarose gels to solid supports (
nitrocellulose filters or nylon membranes ) : 1 . Capillary transfer . In the capillary
...
Page 45
Recover the target DNA fragments containing the inserted kan ' gene by
digesting approximately 30 ug of the pooled plasmid ... Insertion of the fragment
carrying the kan ' gene increases the size of the target fragment by approximately
1 .
Recover the target DNA fragments containing the inserted kan ' gene by
digesting approximately 30 ug of the pooled plasmid ... Insertion of the fragment
carrying the kan ' gene increases the size of the target fragment by approximately
1 .
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