Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 8-39
Other Bacteriophage Vectors Used for cDNA Cloning LORF8 cDNAs inserted into
agt11 have only one chance in six of being expressed in bacteria : Only one half
of the cDNA molecules will be inserted into the vector in the correct orientation ...
Other Bacteriophage Vectors Used for cDNA Cloning LORF8 cDNAs inserted into
agt11 have only one chance in six of being expressed in bacteria : Only one half
of the cDNA molecules will be inserted into the vector in the correct orientation ...
Page 9-9
A solution to this problem is to include a chi sequence in one of the arms of the
vector . The presence of this sequence ... Among the vectors that carry a chi
sequence are EMBL3 and 4 , 12001 , IFIX and ADASH . ( For further discussion
of chi ...
A solution to this problem is to include a chi sequence in one of the arms of the
vector . The presence of this sequence ... Among the vectors that carry a chi
sequence are EMBL3 and 4 , 12001 , IFIX and ADASH . ( For further discussion
of chi ...
Page 9-13
COSMID VECTORS RECOMMENDED FOR CONSTRUCTION OF LIBRARIES
OF EUKARYOTIC GENOMIC DNA The steps ... The DNA of a cosmid vector is
cleaved with appropriate restriction enzyme ( s ) and , in some cases , treated
with ...
COSMID VECTORS RECOMMENDED FOR CONSTRUCTION OF LIBRARIES
OF EUKARYOTIC GENOMIC DNA The steps ... The DNA of a cosmid vector is
cleaved with appropriate restriction enzyme ( s ) and , in some cases , treated
with ...
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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
CONCENTRATING NUCLEIC ACIDS E | 8-10 |
SYNTHESIS OF THE FIRST STRAND OF DNA 8 | 8-11 |
MEASUREMENT OF RADIOACTIVITY IN NUCLEIC ACIDS E | 8-18 |
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Common terms and phrases
aliquots allow amount amplification antibody appropriate approximately bacteriophage bacteriophage T4 base binding buffer carried cDNA cells centrifugation Chapter chromatography cleaved clones colonies complete concentration constructed containing deletions denatured described detection determine digestion dNTPs double-stranded efficiency electrophoresis et al ethanol expression extraction Figure filters four fragment gene genomic DNA hybridization increase Incubate inserted interest isolated Klenow labeled length libraries ligation linear linkers membrane method minutes mixture molecules mRNA mutants nucleic acids nucleotides obtained oligonucleotide plaques 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 step stored strand synthesis target DNA target sequence template termini transfer Tris tube units usually vector volume