Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 35
Collect the cells from a 1 - ml culture by centrifugation at 12 , 000g for 1 minute at
0°C in a microfuge or at 3000 rpm for 5 minutes at 0°C in a Sorvall ... Recover the
cell extract by punching a small hole through the bottom of the microfuge tube .
Collect the cells from a 1 - ml culture by centrifugation at 12 , 000g for 1 minute at
0°C in a microfuge or at 3000 rpm for 5 minutes at 0°C in a Sorvall ... Recover the
cell extract by punching a small hole through the bottom of the microfuge tube .
Page 38
Collect the cells from a l - ml culture by centrifugation at 12 , 000g for 1 minute at
0°C in a microfuge or at 3000 rpm for 5 minutes at 0°C in a ... Using a red - hot
hypodermic needle ( 23 gauge ) , make a hole in the lid of the microfuge tube .
Collect the cells from a l - ml culture by centrifugation at 12 , 000g for 1 minute at
0°C in a microfuge or at 3000 rpm for 5 minutes at 0°C in a ... Using a red - hot
hypodermic needle ( 23 gauge ) , make a hole in the lid of the microfuge tube .
Page 39
the microfuge tube . This is best done with a red - hot hypodermic needle ( 23
gauge ) . Place the microfuge tube containing the glass beads inside an empty
microfuge tube . Centrifuge the piggybacked pair of tubes in a 15 - ml Corex tube
at ...
the microfuge tube . This is best done with a red - hot hypodermic needle ( 23
gauge ) . Place the microfuge tube containing the glass beads inside an empty
microfuge tube . Centrifuge the piggybacked pair of tubes in a 15 - ml Corex tube
at ...
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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