Molecular Cloning: A Laboratory Manual, Volume 1 |
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Page 3-35
CLONING IN COSMID VECTORS DIGESTED WITH TWO RESTRICTION
ENZYMES AND TREATED WITH PHOSPHATASE Ish - Horowicz and Burke (
1981 ) have described a modified procedure for the preparation of cosmid
vectors such as ...
CLONING IN COSMID VECTORS DIGESTED WITH TWO RESTRICTION
ENZYMES AND TREATED WITH PHOSPHATASE Ish - Horowicz and Burke (
1981 ) have described a modified procedure for the preparation of cosmid
vectors such as ...
Page 6-13
In this case , after electrophoresis is completed , stain the gel by soaking it for 30–
45 minutes in a solution of ethidium bromide ( 0.5 mg / ml ) as described on page
6.15 . 11. Turn off the electric current and remove the leads and lid from the gel ...
In this case , after electrophoresis is completed , stain the gel by soaking it for 30–
45 minutes in a solution of ethidium bromide ( 0.5 mg / ml ) as described on page
6.15 . 11. Turn off the electric current and remove the leads and lid from the gel ...
Page 7-45
After use , these solutions should be decontaminated by one of the methods
described in Appendix E. Ultraviolet radiation is dangerous , especially to the
eyes . To minimize exposure , make sure that the ultraviolet light source is
adequately ...
After use , these solutions should be decontaminated by one of the methods
described in Appendix E. Ultraviolet radiation is dangerous , especially to the
eyes . To minimize exposure , make sure that the ultraviolet light source is
adequately ...
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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
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Common terms and phrases
activity agar agarose aliquots allow amount appropriate arms bacterial bacteriophage BamHI buffer carrying cells centrifugation Chapter cloning coli colonies completely concentration construction containing cosmid culture described digestion EcoRI efficiency electrophoresis et al ethanol ethidium ethidium bromide extracts Figure filters final foreign DNA fragments gene genetic genome growth Hindi host hybridization Incubate infected inserted libraries ligase ligation linear method microfuge minutes minutes at 4°C mixture molecules mutations nucleic acids obtained original packaging particles pellet plaques plasmid DNA plate polycloning polymerase possible precipitate prepared presence probes problem procedure promoter protein purified reaction recombinant Recover region remove replication restriction enzyme room temperature Sall segment selection sequences single single-stranded Smal solution step sterile stored strains strand supernatant termini transfer transformation tube usually vector volume Xbal yield