Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 12
Protein A is remarkably resilient and withstands repeated cycles of exposure to
low pH extremely well ; it can also be treated with high concentrations of
denaturing agents such as urea , guanidine hydrochloride , or potassium
isothiocyanate ...
Protein A is remarkably resilient and withstands repeated cycles of exposure to
low pH extremely well ; it can also be treated with high concentrations of
denaturing agents such as urea , guanidine hydrochloride , or potassium
isothiocyanate ...
Page 51
In an Erlenmeyer flask , prepare the appropriate volume of solution containing
the desired concentration of acrylamide for the resolving gel , using the values
given in Table 18 . 3 on page 18 . 52 . Mix the components in the order shown .
In an Erlenmeyer flask , prepare the appropriate volume of solution containing
the desired concentration of acrylamide for the resolving gel , using the values
given in Table 18 . 3 on page 18 . 52 . Mix the components in the order shown .
Page 10
The precipitate of nucleic acid , which is allowed to form in the presence of
moderate concentrations of monovalent cations , is recovered by centrifugation
and redissolved in an appropriate buffer at the desired concentration . The
technique is ...
The precipitate of nucleic acid , which is allowed to form in the presence of
moderate concentrations of monovalent cations , is recovered by centrifugation
and redissolved in an appropriate buffer at the desired concentration . The
technique is ...
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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