Molecular Cloning: A Laboratory Manual, Book 2 |
From inside the book
Results 1-3 of 90
Page 12-4
A few vectors are available that express only the sequences of the foreign protein
(see Chapter 17). More commonly, however, the foreign DNA sequences are
cloned into a restriction site that lies within the coding sequences of a prokaryotic
...
A few vectors are available that express only the sequences of the foreign protein
(see Chapter 17). More commonly, however, the foreign DNA sequences are
cloned into a restriction site that lies within the coding sequences of a prokaryotic
...
Page 2
Several methods have been devised to identify individual clones that synthesize
such proteins in recombinant libraries ... In every case , these methods involve
screening the library with a ligand that binds specifically to the protein of interest .
Several methods have been devised to identify individual clones that synthesize
such proteins in recombinant libraries ... In every case , these methods involve
screening the library with a ligand that binds specifically to the protein of interest .
Page 81
Although both of these methods have yielded much information , they can be
used only with proteins that are available in ... can be identified that map in the
gene coding for the protein of interest and that generate an observable
phenotype .
Although both of these methods have yielded much information , they can be
used only with proteins that are available in ... can be identified that map in the
gene coding for the protein of interest and that generate an observable
phenotype .
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