Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 17
AFFINITY PURIFICATION OF MONOSPECIFIC ANTIBODIES USING ANTIGEN
IMMOBILIZED ON NITROCELLULOSE FILTERS 1 . Load a preparation
containing the target antigen along the entire length of an SDS - polyacrylamide
gel ( see ...
AFFINITY PURIFICATION OF MONOSPECIFIC ANTIBODIES USING ANTIGEN
IMMOBILIZED ON NITROCELLULOSE FILTERS 1 . Load a preparation
containing the target antigen along the entire length of an SDS - polyacrylamide
gel ( see ...
Page 66
Place the nitrocellulose filter on the stack of 3MM paper . Make sure that the filter
is exactly aligned and that no air bubbles are trapped between it and the 3MM
paper . d . Remove the glass plates holding the SDS - polyacrylamide gel from
the ...
Place the nitrocellulose filter on the stack of 3MM paper . Make sure that the filter
is exactly aligned and that no air bubbles are trapped between it and the 3MM
paper . d . Remove the glass plates holding the SDS - polyacrylamide gel from
the ...
Page 68
If the nitrocellulose filter has been dried , float it on the surface of a tray of
deionized water and allow it to wet from beneath by capillary action . Then ,
submerge the filter in the water for at least 5 minutes to displace trapped air
bubbles . 2 .
If the nitrocellulose filter has been dried , float it on the surface of a tray of
deionized water and allow it to wet from beneath by capillary action . Then ,
submerge the filter in the water for at least 5 minutes to displace trapped air
bubbles . 2 .
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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