Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 27
The chief practical advantage of this procedure is that no synthesis of the second
strand of cDNA is required . Furthermore , the procedure should , in theory , allow
the sequences at the 5 ' terminus of the mRNA ( which are often lost ...
The chief practical advantage of this procedure is that no synthesis of the second
strand of cDNA is required . Furthermore , the procedure should , in theory , allow
the sequences at the 5 ' terminus of the mRNA ( which are often lost ...
Page 70
Allow the slurry to settle for a few minutes and then release the hemostat . The
column will form as the buffer drips from the pipette . If necessary , add more
Sepharose CL - 4B until the packed matrix almost fills the pipette . Wash the
column ...
Allow the slurry to settle for a few minutes and then release the hemostat . The
column will form as the buffer drips from the pipette . If necessary , add more
Sepharose CL - 4B until the packed matrix almost fills the pipette . Wash the
column ...
Page 22
5 volumes of lysis solution in beakers . Allow the powders to spread over the
surface of the lysis solution , and then shake the beakers to submerge the
material . When all the material is in solution , transfer the solutions to centrifuge
tubes . 3 .
5 volumes of lysis solution in beakers . Allow the powders to spread over the
surface of the lysis solution , and then shake the beakers to submerge the
material . When all the material is in solution , transfer the solutions to centrifuge
tubes . 3 .
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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
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