Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 38
Grow a 2 - ml culture of E . coli strain Y1089 to saturation in LB medium
containing 0 . 2 % maltose , 50 ug / ml ampicillin , and 10 mm MgCl , . 3 . Dilute
50 ul of the saturated culture with 2 ml of LB medium containing 10 mm MgCl , .
Transfer ...
Grow a 2 - ml culture of E . coli strain Y1089 to saturation in LB medium
containing 0 . 2 % maltose , 50 ug / ml ampicillin , and 10 mm MgCl , . 3 . Dilute
50 ul of the saturated culture with 2 ml of LB medium containing 10 mm MgCl , .
Transfer ...
Page 39
Add 50 ul of each culture to 4 ml of prewarmed ( 30°C ) LB medium containing 50
ug / ml ampicillin . Continue incubation at 30°C with vigorous agitation . 9 . Grow
the cultures until the OD 600 = 0 . 45 ( ~ 3 hours of incubation ) . It is essential ...
Add 50 ul of each culture to 4 ml of prewarmed ( 30°C ) LB medium containing 50
ug / ml ampicillin . Continue incubation at 30°C with vigorous agitation . 9 . Grow
the cultures until the OD 600 = 0 . 45 ( ~ 3 hours of incubation ) . It is essential ...
Page 76
Add 5 ml of a mid - log - phase culture of E . coli strain CJ236 ( dut ung F ' ) (
Kunkel et al . 1987 ) . Incubate the culture with vigorous shaking ( 300 cycles /
minute on a rotary shaker ) for 6 hours at 37°C . The bacteriophage suspension
used ...
Add 5 ml of a mid - log - phase culture of E . coli strain CJ236 ( dut ung F ' ) (
Kunkel et al . 1987 ) . Incubate the culture with vigorous shaking ( 300 cycles /
minute on a rotary shaker ) for 6 hours at 37°C . The bacteriophage suspension
used ...
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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
TEST LIGATION 3 29 | 3 |
SYNTHESIS OF THE FIRST STRAND OF cDNA 8 | 11 |
FRAGMENT OF E coli DNA POLYMERASE I 13 59 | 14 |
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Common terms and phrases
acid activity agarose aliquots allow amount amplification appropriate approximately bacteriophage bacteriophage T4 base buffer carried cDNA cells centrifugation Chapter chromatography cleaved clones colonies concentration constructed containing deletions denatured described determine digestion DNA polymerase dNTPs double-stranded efficiency electrophoresis et al ethanol expression Figure filters fragment gene genomic hybridization increase Incubate inserted interest isolated labeled length libraries ligation linear linkers method microfuge minutes mixture molecules mRNA mutagenesis mutagenic mutations Nucleic nucleotides obtained oligonucleotide original plaques plasmid plasmid DNA plate pool position possible prepared presence primer probe problem protein purified radiolabeled reaction recombinant region remove restriction enzyme room temperature samples screening sequence single single-stranded solution specific step Store strand synthesis target DNA target sequence template termini tion transfer transformants tube units usually vector volume