Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 5
cDNA synthesized from mammalian mRNA should run as a continuous smear
from approximately 500 bases to more than 5 kb ( Figure 8 . 2 ) . The bulk of the
radioactivity should lie between 1 . 5 kb and 2 kb , and there should be no
specific ...
cDNA synthesized from mammalian mRNA should run as a continuous smear
from approximately 500 bases to more than 5 kb ( Figure 8 . 2 ) . The bulk of the
radioactivity should lie between 1 . 5 kb and 2 kb , and there should be no
specific ...
Page 37
However , to allow a margin of safety , cDNA estimated to be larger than
approximately 6 kb should be cloned in a vector with a greater capacity ( see
Kaiser and Murray 1985 ) . For a more detailed description of gt10 , see Chapter
2 , page 2 .
However , to allow a margin of safety , cDNA estimated to be larger than
approximately 6 kb should be cloned in a vector with a greater capacity ( see
Kaiser and Murray 1985 ) . For a more detailed description of gt10 , see Chapter
2 , page 2 .
Page 32
The bottom of the strip should dip into a petri dish filled to a level of approximately
0 . 5 cm with developing buffer ( 0 . 5 m ammonium bicarbonate ) . Cover the jar
and allow the chromatograph to develop until the solvent front has migrated ...
The bottom of the strip should dip into a petri dish filled to a level of approximately
0 . 5 cm with developing buffer ( 0 . 5 m ammonium bicarbonate ) . Cover the jar
and allow the chromatograph to develop until the solvent front has migrated ...
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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