Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 35
... in step 4 ) . During treatment with chloroquine , it is normal for cells to develop
a vesicularized appearance . After the 3 - 5 - hour treatment with DNA and
chloroquine , remove the medium and the precipitate , wash with PBS , and add 5
ml of ...
... in step 4 ) . During treatment with chloroquine , it is normal for cells to develop
a vesicularized appearance . After the 3 - 5 - hour treatment with DNA and
chloroquine , remove the medium and the precipitate , wash with PBS , and add 5
ml of ...
Page 38
Recover the washed cells by centrifugation , and again discard the supernatant .
3 . Gently resuspend 1 x 10 ' cells in 1 ml of ... for 5 minutes at room temperature ,
and wash them once with PBS . Resuspend the cells in 10 ml of prewarmed ...
Recover the washed cells by centrifugation , and again discard the supernatant .
3 . Gently resuspend 1 x 10 ' cells in 1 ml of ... for 5 minutes at room temperature ,
and wash them once with PBS . Resuspend the cells in 10 ml of prewarmed ...
Page 45
Several different buffers are commonly used to wash protein A - antigen -
antibody complexes . The aim is to displace ... The tighter the binding between
antibody and antigen , the more stringent the washing conditions can be . The
buffer best ...
Several different buffers are commonly used to wash protein A - antigen -
antibody complexes . The aim is to displace ... The tighter the binding between
antibody and antigen , the more stringent the washing conditions can be . The
buffer best ...
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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