Molecular Cloning: A Laboratory Manual, Book 2 |
From inside the book
Results 1-3 of 64
Page 15-7
Enzymes that generate blunt ends ( FnuDII , AluI , Rsal , and HaeIII ) are
particularly useful because they allow the direct addition of a large variety of
synthetic linkers . However , enzymes that cleave in a staggered fashion can be
used if the ...
Enzymes that generate blunt ends ( FnuDII , AluI , Rsal , and HaeIII ) are
particularly useful because they allow the direct addition of a large variety of
synthetic linkers . However , enzymes that cleave in a staggered fashion can be
used if the ...
Page 15-10
Amount of linker ( in nanograms ) = x / y x 2 x 100 where x = length of linker ( in
nucleotides ) , y = length of linear plasmid DNA ( in nucleotides ) , and z = desired
molar ratio of linkers to target DNA . Usually , a 20 - to 30 - fold molar excess of ...
Amount of linker ( in nanograms ) = x / y x 2 x 100 where x = length of linker ( in
nucleotides ) , y = length of linear plasmid DNA ( in nucleotides ) , and z = desired
molar ratio of linkers to target DNA . Usually , a 20 - to 30 - fold molar excess of ...
Page 15-85
INSERTION OF HEXAMERIC LINKERS INTO PROTEIN - CODING SEQUENCES
The method given below , which is an elaboration of the work of Boeke ( 1981 ) ,
is based on protocols published by Barany ( 1985a , b , 1987 , 1988 ) .
INSERTION OF HEXAMERIC LINKERS INTO PROTEIN - CODING SEQUENCES
The method given below , which is an elaboration of the work of Boeke ( 1981 ) ,
is based on protocols published by Barany ( 1985a , b , 1987 , 1988 ) .
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
DNA METHYLATION 5 | 8-5 |
SOLUTIONS FOR WORKING WITH BACTERIOPHAGEI A | 8-7 |
SYNTHESIS OF THE FIRST STRAND OF DNA 8 | 8-11 |
93 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 isolation 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 vectors volume