Molecular Cloning: A Laboratory Manual, Book 2 |
From inside the book
Results 1-3 of 87
Page 9-92
The average distance between EcoRI sites in the mammalian genome is
approximately 4 kb ( Botchan et al . 1974 ) , and complete digests therefore
contain approximately 100 different fragments of DNA . Consequently , a library
constructed ...
The average distance between EcoRI sites in the mammalian genome is
approximately 4 kb ( Botchan et al . 1974 ) , and complete digests therefore
contain approximately 100 different fragments of DNA . Consequently , a library
constructed ...
Page 11-32
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 ...
Page 15-67
Oligonucleotides will remain at the origin , whereas ATP and inorganic
phosphate will migrate in the same direction as the solvent ( inorganic phosphate
migrates slightly slower than the solvent front and ATP is approximately
equidistant ...
Oligonucleotides will remain at the origin , whereas ATP and inorganic
phosphate will migrate in the same direction as the solvent ( inorganic phosphate
migrates slightly slower than the solvent front and ATP is approximately
equidistant ...
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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
CONCENTRATING NUCLEIC ACIDS E | 8-10 |
SYNTHESIS OF THE FIRST STRAND OF DNA 8 | 8-11 |
MEASUREMENT OF RADIOACTIVITY IN NUCLEIC ACIDS E | 8-18 |
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Common terms and phrases
aliquots allow amount amplification antibody appropriate approximately bacteriophage bacteriophage T4 base binding buffer carried cDNA cells centrifugation Chapter chromatography cleaved clones colonies complete concentration constructed containing deletions denatured described detection determine digestion dNTPs double-stranded efficiency electrophoresis et al ethanol expression extraction Figure filters four fragment gene genomic DNA hybridization increase Incubate inserted interest isolated Klenow labeled length libraries ligation linear linkers membrane method minutes mixture molecules mRNA mutants nucleic acids nucleotides obtained oligonucleotide plaques plasmid DNA plate position possible precipitation prepared presence primer probe problem protein purified radioactivity radiolabeled reaction recombinant region remove restriction enzyme room temperature samples screening separate sequence single single-stranded solution step stored strand synthesis target DNA target sequence template termini transfer Tris tube units usually vector volume