Molecular Cloning: A Laboratory Manual, Volume 1 |
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Results 1-3 of 64
Page 125
Remove the medium by aspiration , leaving the bacterial pellet as dry as possible
. The supernatant can be conveniently removed with a disposable pipette tip
attached to a vacuum line ( see Figure 1.3 ) . Use a gentle vacuum and touch the
tip ...
Remove the medium by aspiration , leaving the bacterial pellet as dry as possible
. The supernatant can be conveniently removed with a disposable pipette tip
attached to a vacuum line ( see Figure 1.3 ) . Use a gentle vacuum and touch the
tip ...
Page 7-21
Check that the pellet of RNA has not fallen out of the tube . Depending on the
amount of RNA present , the pellet may be invisible in the tube , but it can be
seen easily enough if it falls onto the pad of Kimwipes . Should this occur , use
sterile ...
Check that the pellet of RNA has not fallen out of the tube . Depending on the
amount of RNA present , the pellet may be invisible in the tube , but it can be
seen easily enough if it falls onto the pad of Kimwipes . Should this occur , use
sterile ...
Page 7-24
Dissolve the pellet in a small volume of guanidine HCl homogenization buffer II .
Use 10-15 ml of buffer for every gram of original cells or tissue . The pellet is often
difficult to dissolve , and it may be necessary to use a homogenizer to assist in ...
Dissolve the pellet in a small volume of guanidine HCl homogenization buffer II .
Use 10-15 ml of buffer for every gram of original cells or tissue . The pellet is often
difficult to dissolve , and it may be necessary to use a homogenizer to assist in ...
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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
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