Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 14
AMPLIFICATION METHODS Precautions Because the polymerase chain reaction
is capable of amplifying as little as a single molecule of DNA , precautions should
be taken to guard against contamination of the reaction mixture with trace ...
AMPLIFICATION METHODS Precautions Because the polymerase chain reaction
is capable of amplifying as little as a single molecule of DNA , precautions should
be taken to guard against contamination of the reaction mixture with trace ...
Page 1-2
See Polymerase chain reaction of gene copy number in mammalian cells using
adenosine deaminase, 16.29 using dihydrofolate reductase, 16.28-16.29 of
genomic DNA library in bacteriophage X, 9.30 of plasmid DNA using
chloramphenicol ...
See Polymerase chain reaction of gene copy number in mammalian cells using
adenosine deaminase, 16.29 using dihydrofolate reductase, 16.28-16.29 of
genomic DNA library in bacteriophage X, 9.30 of plasmid DNA using
chloramphenicol ...
Page 43
See also Klenow fragment ( large fragment ) of E . coli DNA polymerase I ; T4
bacteriophage , DNA polymerase Subtracted probes . See Probes Sucrose
density gradients containing methylmercuric hydroxide , for RNA , 7 . 35 – 7 .
See also Klenow fragment ( large fragment ) of E . coli DNA polymerase I ; T4
bacteriophage , DNA polymerase Subtracted probes . See Probes Sucrose
density gradients containing methylmercuric hydroxide , for RNA , 7 . 35 – 7 .
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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