Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 59
Remove the medium from cells growing in monolayers in 90 - mm tissue culture
dishes by gentle aspiration . Wash the monolayers three times with 5 ml of
phosphate - buffered saline ( PBS ; see Appendix B ) lacking magnesium and
calcium ...
Remove the medium from cells growing in monolayers in 90 - mm tissue culture
dishes by gentle aspiration . Wash the monolayers three times with 5 ml of
phosphate - buffered saline ( PBS ; see Appendix B ) lacking magnesium and
calcium ...
Page 14
Antibodies that are directed against specific contaminating antigens ( e . g . ,
bacterial antigens ) can be removed by adsorption . ... Methods to remove
antibacterial antibodies from antisera used for such screening are described on
pages 12 .
Antibodies that are directed against specific contaminating antigens ( e . g . ,
bacterial antigens ) can be removed by adsorption . ... Methods to remove
antibacterial antibodies from antisera used for such screening are described on
pages 12 .
Page 15
Removal of Cross - reacting Antibodies from Antisera To remove antibodies that
react with antigens present in mammalian cells , use an acetone extract of a cell
line or tissue that is known not to express the true target antigen . If such a cell ...
Removal of Cross - reacting Antibodies from Antisera To remove antibodies that
react with antigens present in mammalian cells , use an acetone extract of a cell
line or tissue that is known not to express the true target antigen . If such a cell ...
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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