Molecular Cloning: A Laboratory Manual, Book 2 |
From inside the book
Results 1-3 of 77
Page viii
77 PELLETING BACTERIOPHAGE PARTICLES 2 . 77 GLYCEROL STEP
GRADIENT 2 . 78 EQUILIBRIUM CENTRIFUGATION IN CESIUM CHLORIDE 2 .
79 EXTRACTION OF BACTERIOPHAGE DNA 2 . 80 Cloning in Bacteriophage i 2
.
77 PELLETING BACTERIOPHAGE PARTICLES 2 . 77 GLYCEROL STEP
GRADIENT 2 . 78 EQUILIBRIUM CENTRIFUGATION IN CESIUM CHLORIDE 2 .
79 EXTRACTION OF BACTERIOPHAGE DNA 2 . 80 Cloning in Bacteriophage i 2
.
Page 9-16
Transfer the cell suspension to a centrifuge tube stored on ice . Wash the petri
dish with 1 ml of TBS , and combine the washing with the cell suspension in the
centrifuge tube . Recover the cells by centrifugation at 1500g for 10 minutes at 4°
C ...
Transfer the cell suspension to a centrifuge tube stored on ice . Wash the petri
dish with 1 ml of TBS , and combine the washing with the cell suspension in the
centrifuge tube . Recover the cells by centrifugation at 1500g for 10 minutes at 4°
C ...
Page 15-21
Purify the closed circular recombinant DNA ( s ) by equilibrium centrifugation in
CsCl - ethidium bromide gradients ( see Chapter 1 , pages 1.421.44 ) . It is
essential to use highly purified closed circular DNA for two reasons : ( 1 ) to
minimize ...
Purify the closed circular recombinant DNA ( s ) by equilibrium centrifugation in
CsCl - ethidium bromide gradients ( see Chapter 1 , pages 1.421.44 ) . It is
essential to use highly purified closed circular DNA for two reasons : ( 1 ) to
minimize ...
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