Molecular Cloning: A Laboratory Manual, Book 2 |
From inside the book
Results 1-3 of 21
Page 44
cDNAs up to 10 kb in length may be inserted into this site and expressed in either
infected bacteria or induced lysogens , essentially as described for 1gt11 . In
addition , AZAP fusion proteins may be expressed from high - copy - number ...
cDNAs up to 10 kb in length may be inserted into this site and expressed in either
infected bacteria or induced lysogens , essentially as described for 1gt11 . In
addition , AZAP fusion proteins may be expressed from high - copy - number ...
Page 16
Incubate the infected bacteria for 20 minutes at 37°C . Immunological screening
works best when the density of plaques is low . The color produced by the
chromogenic reaction is most intense at the expanding edge of the plaque .
Incubate the infected bacteria for 20 minutes at 37°C . Immunological screening
works best when the density of plaques is low . The color produced by the
chromogenic reaction is most intense at the expanding edge of the plaque .
Page 76
5 hours Plaque - purify recombinant bacteriophage ; make sure that single -
stranded DNA is prepared from an infected culture grown for not more than 4 . 5
hours Titrate primer or use an alternative primer Repurify primer Titrate primer ...
5 hours Plaque - purify recombinant bacteriophage ; make sure that single -
stranded DNA is prepared from an infected culture grown for not more than 4 . 5
hours Titrate primer or use an alternative primer Repurify primer Titrate primer ...
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