Molecular Cloning: A Laboratory Manual, Volume 1 |
From inside the book
Results 1-3 of 40
Page 2-34
... Xbal 34070 Pvul 32770 Sacl 33990 Bgill -32770 Xhol 32770 BamHI 32760 Hindill 29160 Bgill 29020 Bgill 26240 Pvul 26160 Bgill 25290 San 24790 Sall 23660 Smal 32760 EcoRI 32760 Xbal 20020 Xbal -20010 EcoRI 20010 Hindill 20000 BamHI 19400 ...
... Xbal 34070 Pvul 32770 Sacl 33990 Bgill -32770 Xhol 32770 BamHI 32760 Hindill 29160 Bgill 29020 Bgill 26240 Pvul 26160 Bgill 25290 San 24790 Sall 23660 Smal 32760 EcoRI 32760 Xbal 20020 Xbal -20010 EcoRI 20010 Hindill 20000 BamHI 19400 ...
Page 2-36
... Xbal 34310 Bg / ll 32800 Sall 34080 Pvul 34000 Bgfl 32780 EcoRI 32780 BamHI 32770 Hindill -32770 Sacl 32770 Xhol 29160 Bgl 29020 Bgill 26240 Pvul 26160 Bgill 25290 Sall 24790 Sall 23660 Smal 32760 Xbal 20040 Xbal -20030 Xhol 20030 Sacl ...
... Xbal 34310 Bg / ll 32800 Sall 34080 Pvul 34000 Bgfl 32780 EcoRI 32780 BamHI 32770 Hindill -32770 Sacl 32770 Xhol 29160 Bgl 29020 Bgill 26240 Pvul 26160 Bgill 25290 Sall 24790 Sall 23660 Smal 32760 Xbal 20040 Xbal -20030 Xhol 20030 Sacl ...
Page 2-38
... Xbal 34080 Pvul 32790 Sacl 34000 Bgl 32770 Sall 32760 Xhol 32760 EcoRI 32760 Xbal 29160 Bgl 29020 Bgl 26240 Pvul 26160 Bgill 25290 Sall 24790 Sall 23660 Smal 19400 Smal 18560 Kpnl 17050 Kpnl 11930 Pvul 20030 Xbal 20030 EcoRI 20020 Xhol ...
... Xbal 34080 Pvul 32790 Sacl 34000 Bgl 32770 Sall 32760 Xhol 32760 EcoRI 32760 Xbal 29160 Bgl 29020 Bgl 26240 Pvul 26160 Bgill 25290 Sall 24790 Sall 23660 Smal 19400 Smal 18560 Kpnl 17050 Kpnl 11930 Pvul 20030 Xbal 20030 EcoRI 20020 Xhol ...
Contents
Essential Features of Plasmids 1 | 1-3 |
Staininging RNA Before and After Transfer to Nitrocellulose Filters 7 51 | 1-7 |
Index | 1-8 |
Copyright | |
95 other sections not shown
Other editions - View all
Common terms and phrases
activity agar agarose aliquots allow amount appropriate arms bacterial bacteriophage BamHI buffer carrying cells centrifugation Chapter cloning coli colonies competent 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 gradients growth Hindill host hybridization Incubate infected inserted libraries ligase ligation linear method microfuge minutes minutes at 4°C mixture molecules mutations Nucleic Acids obtained original packaging pellet plaques plasmid DNA plate polycloning polymerase possible precipitate prepared presence probes procedure protein purified Pvul reaction recA recombinant Recover region remove replication restriction enzyme resulting room temperature Sall screening segment selection sequences single single-stranded Smal solution step sterile stored strains strand supernatant termini transfer transformation tube usually vector volume yield