Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 10
A Laboratory Manual Joseph Sambrook, E. F. Fritsch, Tom Maniatis. 2 . If an
amino acid with six possible codons must be used , synthesize two separate
pools of oligonucleotides so that only the six correct codons are represented . In
the case ...
A Laboratory Manual Joseph Sambrook, E. F. Fritsch, Tom Maniatis. 2 . If an
amino acid with six possible codons must be used , synthesize two separate
pools of oligonucleotides so that only the six correct codons are represented . In
the case ...
Page 15
It is possible , and often desirable , to synthesize a small pool of 2 - 8 guessmers
that contains all possible choices at certain positions . It is best to carry out this
kind of limited substitution when an amino acid whose codon is highly
degenerate ...
It is possible , and often desirable , to synthesize a small pool of 2 - 8 guessmers
that contains all possible choices at certain positions . It is best to carry out this
kind of limited substitution when an amino acid whose codon is highly
degenerate ...
Page 82
It is therefore possible to selectively label a designated terminus with the
appropriate [ * ? P ] dNTP and the Klenow fragment of E . coli DNA polymerase I .
In the example shown in Figure 13 . 11 , a recombinant plasmid carrying the
target at ...
It is therefore possible to selectively label a designated terminus with the
appropriate [ * ? P ] dNTP and the Klenow fragment of E . coli DNA polymerase I .
In the example shown in Figure 13 . 11 , a recombinant plasmid carrying the
target at ...
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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