Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 17
Oligonucleotides That Contain a Neutral Base at Positions of Degeneracy Probes
of this type are used to reduce the degeneracy of pools of oligonucleotides . At
positions where there is a choice of two , three , or four conventional bases , a ...
Oligonucleotides That Contain a Neutral Base at Positions of Degeneracy Probes
of this type are used to reduce the degeneracy of pools of oligonucleotides . At
positions where there is a choice of two , three , or four conventional bases , a ...
Page 11
In this procedure ( Maxam and Gilbert 1980 ) , a fragment of DNA radiolabeled at
one end is partially cleaved in five separate chemical reactions , each of which is
specific for a particular base or type of base . This generates five populations of ...
In this procedure ( Maxam and Gilbert 1980 ) , a fragment of DNA radiolabeled at
one end is partially cleaved in five separate chemical reactions , each of which is
specific for a particular base or type of base . This generates five populations of ...
Page 100
One or a few bands in two ladders pro - duced by cleavage reactions that do not
normally share base specificity . Cleavage is consistent with base specificity
everywhere else in the sequencing pattern . 13 . Difficulty in identifying the band
...
One or a few bands in two ladders pro - duced by cleavage reactions that do not
normally share base specificity . Cleavage is consistent with base specificity
everywhere else in the sequencing pattern . 13 . Difficulty in identifying the band
...
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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 |
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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