Molecular Cloning: A Laboratory Manual, Book 3 |
From inside the book
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Page 9
lines of cells that permanently express more modest levels of the transfected
genes . Genes encoding selectable markers DNA , which enters only a small
proportion of mammalian cells in a given culture , becomes stably maintained in
an ...
lines of cells that permanently express more modest levels of the transfected
genes . Genes encoding selectable markers DNA , which enters only a small
proportion of mammalian cells in a given culture , becomes stably maintained in
an ...
Page 38
While the precipitate is forming , collect the exponentially growing cells by
centrifugation at 800g for 5 minutes at 4°C . Discard the supernatant , and
resuspend the cell pellet in 20 volumes of ice - cold phosphate - buffered saline (
PBS ; see ...
While the precipitate is forming , collect the exponentially growing cells by
centrifugation at 800g for 5 minutes at 4°C . Discard the supernatant , and
resuspend the cell pellet in 20 volumes of ice - cold phosphate - buffered saline (
PBS ; see ...
Page 70
Furthermore , because the cellular machinery for transcription , translation , and
processing are very uniform across all mammalian species , a single gene
transferred to cells from a different species could be expected to be expressed in
a ...
Furthermore , because the cellular machinery for transcription , translation , and
processing are very uniform across all mammalian species , a single gene
transferred to cells from a different species could be expected to be expressed in
a ...
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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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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