Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 5
The eukaryotic transcription unit consists of noncoding sequences and
sequences coding for selectable markers . It is frequently assembled as a
composite of elements derived from different , well - characterized viral or
mammalian genes .
The eukaryotic transcription unit consists of noncoding sequences and
sequences coding for selectable markers . It is frequently assembled as a
composite of elements derived from different , well - characterized viral or
mammalian genes .
Page 18
The genome is functionally divided into early and late regions , which are
transcribed from the two DNA strands in opposite ... the viral early and late
transcription units and contains a number of different controlling cis elements (
see Figure 16 .
The genome is functionally divided into early and late regions , which are
transcribed from the two DNA strands in opposite ... the viral early and late
transcription units and contains a number of different controlling cis elements (
see Figure 16 .
Page 56
The accuracy with which transcripts are initiated can be determined by mapping
the precise location of the 5 ' terminus of the ... In most cases , therefore , the
ability of the cis - acting elements to modulate the rate of transcription is not
assayed ...
The accuracy with which transcripts are initiated can be determined by mapping
the precise location of the 5 ' terminus of the ... In most cases , therefore , the
ability of the cis - acting elements to modulate the rate of transcription is not
assayed ...
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Contents
BOOK | 3 |
Identification and Analysis of Recombinants 2 108 | 30 |
TRANSFECTION MEDIATED BY DEAEDEXTRAN 16 | 41 |
Copyright | |
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Common terms and phrases
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