Molecular Cloning: A Laboratory Manual, Book 2 |
From inside the book
Results 1-3 of 64
Page 56
It has therefore been possible to use oligonucleotides of defined sequence to
probe fetal DNA for the presence of specific point mutations that cause conditions
such as sickle - cell anemia ( Conner et al . 1983 ) , certain thalassemias ( Orkin
et ...
It has therefore been possible to use oligonucleotides of defined sequence to
probe fetal DNA for the presence of specific point mutations that cause conditions
such as sickle - cell anemia ( Conner et al . 1983 ) , certain thalassemias ( Orkin
et ...
Page 51
In contrast to most other methods of mutagenesis , which typically spawn mixed
populations of variants , oligonucleotide - mediated mutagenesis specifically
generates mutations designed by the experimenter . Because of this precision ,
the ...
In contrast to most other methods of mutagenesis , which typically spawn mixed
populations of variants , oligonucleotide - mediated mutagenesis specifically
generates mutations designed by the experimenter . Because of this precision ,
the ...
Page 81
A less direct type of analysis may be used if naturally occurring mutations can be
identified that map in the gene coding for the protein of interest and that generate
an observable phenotype . The mutant genes can then be cloned , and their ...
A less direct type of analysis may be used if naturally occurring mutations can be
identified that map in the gene coding for the protein of interest and that generate
an observable phenotype . The mutant genes can then be cloned , and their ...
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
TEST LIGATION 3 29 | 3 |
SYNTHESIS OF THE FIRST STRAND OF cDNA 8 | 11 |
FRAGMENT OF E coli DNA POLYMERASE I 13 59 | 14 |
Copyright | |
92 other sections not shown
Other editions - View all
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