Molecular Cloning: A Laboratory Manual, Book 2 |
From inside the book
Results 1-3 of 72
Page 8-66
To all four aliquots , add 100 ng of a plasmid such as Xf3 or PBR322 that has
been digested to completion with Psti , purified by extraction with phenol :
chloroform and precipitation with ethanol , and dissolved in TE ( pH 8.0 ) at a
concentration ...
To all four aliquots , add 100 ng of a plasmid such as Xf3 or PBR322 that has
been digested to completion with Psti , purified by extraction with phenol :
chloroform and precipitation with ethanol , and dissolved in TE ( pH 8.0 ) at a
concentration ...
Page 10-20
The Km of the enzyme is different for each of the four dNTPs ( Travaglini et al .
1975 ) : dGTP MCTP DATP dTTP 45 um 200 um 12 um 140 uM When the
concentration of each of the four dNTPs in the reaction is greater than Km , the
synthesis ...
The Km of the enzyme is different for each of the four dNTPs ( Travaglini et al .
1975 ) : dGTP MCTP DATP dTTP 45 um 200 um 12 um 140 uM When the
concentration of each of the four dNTPs in the reaction is greater than Km , the
synthesis ...
Page 13-100
An extraneous band across all four lad - ders at one position in a sequencing
pattern . Some double - stranded DNA molecules are Attempt to derive the
sequence surrounding nicked by a restriction enzyme at a se the break on both
strands ...
An extraneous band across all four lad - ders at one position in a sequencing
pattern . Some double - stranded DNA molecules are Attempt to derive the
sequence surrounding nicked by a restriction enzyme at a se the break on both
strands ...
What people are saying - Write a review
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
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 |
90 other sections not shown
Other editions - View all
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