Molecular Cloning: A Laboratory Manual, Volume 1 |
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Page xxxv
Radiolabeling the Target Protein 18.26 RADIOLABELING MAMMALIAN CELLS
WITH ( SJMETHIONINE AND [ S ] CYSTEINE 18.27 METABOLIC
RADIOLABELING OF PROTEINS EXPRESSED IN YEASTS AND BACTERIA
18.29 Lysis of Cells ...
Radiolabeling the Target Protein 18.26 RADIOLABELING MAMMALIAN CELLS
WITH ( SJMETHIONINE AND [ S ] CYSTEINE 18.27 METABOLIC
RADIOLABELING OF PROTEINS EXPRESSED IN YEASTS AND BACTERIA
18.29 Lysis of Cells ...
Page 2-5
The N protein is therefore a positive regulatory element whose activity is
necessary for the lytic growth of bacteriophages carrying ... ( ori ) ( see Figure 2.2
) , which is activated by two virus - encoded proteins , the products of the O and P
genes .
The N protein is therefore a positive regulatory element whose activity is
necessary for the lytic growth of bacteriophages carrying ... ( ori ) ( see Figure 2.2
) , which is activated by two virus - encoded proteins , the products of the O and P
genes .
Page 2-7
Further maturation , which involves removal of the scaffolding protein and
proteolytic processing of other components , depends on a protein ( the groE
gene product ) supplied by the host . The resulting structures are called preheads
.
Further maturation , which involves removal of the scaffolding protein and
proteolytic processing of other components , depends on a protein ( the groE
gene product ) supplied by the host . The resulting structures are called preheads
.
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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