Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 2
The development of methods for the introduction of DNA into cultured
mammalian cells has made it possible to express cloned genes in a broad range
of cell types from different species . These methods have been used to
overproduce ...
The development of methods for the introduction of DNA into cultured
mammalian cells has made it possible to express cloned genes in a broad range
of cell types from different species . These methods have been used to
overproduce ...
Page 3
In addition , production of authentic , biologically active eukaryotic proteins from
cloned DNA frequently requires posttranslational modifications such as accurate
disulfide bond formation , glycosylation , phosphorylation , oligomerization , or ...
In addition , production of authentic , biologically active eukaryotic proteins from
cloned DNA frequently requires posttranslational modifications such as accurate
disulfide bond formation , glycosylation , phosphorylation , oligomerization , or ...
Page 11
To provide a pi promoter to direct transcription of a cloned gene that has an E .
coli ribosome - binding site : 1 . Digest pKC30 with Hpal . 2 . Digest the cloned
DNA with appropriate restriction enzymes at a position 5 ' of the initiation codon
and ...
To provide a pi promoter to direct transcription of a cloned gene that has an E .
coli ribosome - binding site : 1 . Digest pKC30 with Hpal . 2 . Digest the cloned
DNA with appropriate restriction enzymes at a position 5 ' of the initiation codon
and ...
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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
BOOK | 3 |
Identification and Analysis of Recombinants 2 108 | 30 |
TRANSFECTION MEDIATED BY DEAEDEXTRAN 16 | 41 |
Copyright | |
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acetate activity added Adjust aliquots allow amount antibody antigen Appendix appropriate approximately aqueous assay bacterial bacteriophage base binding buffer carried cells centrifugation Chapter chromatography Cl pH cloned coli column complete concentration containing culture deionized water described desired detected dilution Dissolve EDTA efficiency electrophoresis enzyme et al ethanol expression extract Figure filter final fragment gene growth hybridization Incubate levels ligation mammalian cells medium method mg/ml microfuge tube minutes mixture mRNAs nucleic acid pellet phase phosphate Place plasmid plate polymerase precipitation prepared procedure Products promoter protein radioactive radiolabeled reaction remove restriction room temperature sample screen selection sequence sodium solution specific step sterile stored strain TABLE Telephone termini tion transcription transfection transfer transformation Tris ug/ml usually vectors volume wash western blotting ОН