Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 62
In case of contact , immediately flush eyes or skin with copious amounts of water .
Discard contaminated clothing . PMSF , which is labile in aqueous solutions ,
should be added from a stock solution just before the suspension buffer is used .
In case of contact , immediately flush eyes or skin with copious amounts of water .
Discard contaminated clothing . PMSF , which is labile in aqueous solutions ,
should be added from a stock solution just before the suspension buffer is used .
Page 2
Which of the four dNTPs are added to the reaction depends on ( 1 ) the sequence
of the protuding 5 ' termini at the end ( s ) of the DNA and ( 2 ) whether partial or
complete filling is required . For example , to fill recessed 3 ' termini created by ...
Which of the four dNTPs are added to the reaction depends on ( 1 ) the sequence
of the protuding 5 ' termini at the end ( s ) of the DNA and ( 2 ) whether partial or
complete filling is required . For example , to fill recessed 3 ' termini created by ...
Page 10
Ligate the fragment of DNA carrying the newly added linkers to a fragment that
carries compatible termini . Note The effectiveness of the restriction enzyme
digestion can be tested as follows : a . Before adding the enzyme in step 3 ,
remove 2 ...
Ligate the fragment of DNA carrying the newly added linkers to a fragment that
carries compatible termini . Note The effectiveness of the restriction enzyme
digestion can be tested as follows : a . Before adding the enzyme in step 3 ,
remove 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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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