Molecular Cloning: A Laboratory Manual, Book 2 |
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Page 30
5 ml of melted top agar or agarose with each aliquot of infected bacteria and
spread on a freshly poured 150 - mm plate of bottom agar . Alternatively , as
many as 450 , 000 bacteriophages may be mixed with 14 ml of bacteria and
plated in 75 ...
5 ml of melted top agar or agarose with each aliquot of infected bacteria and
spread on a freshly poured 150 - mm plate of bottom agar . Alternatively , as
many as 450 , 000 bacteriophages may be mixed with 14 ml of bacteria and
plated in 75 ...
Page 23
A Laboratory Manual Joseph Sambrook, E. F. Fritsch, Tom Maniatis. METHOD 2
This method is used to transfer many bacterial colonies simultaneously from the
surface of an agar plate to a nitrocellulose filter . The method works with bacterial
...
A Laboratory Manual Joseph Sambrook, E. F. Fritsch, Tom Maniatis. METHOD 2
This method is used to transfer many bacterial colonies simultaneously from the
surface of an agar plate to a nitrocellulose filter . The method works with bacterial
...
Page 65
5 ml of 2 x YT top agar ( melted and cooled to 45°C ) to each culture , and plate
each mixture on a separate YT agar plate . Incubate the plates for 16 hours at 37°
C to allow plaques to form . If mutagenesis is carried out by the Kunkel method ...
5 ml of 2 x YT top agar ( melted and cooled to 45°C ) to each culture , and plate
each mixture on a separate YT agar plate . Incubate the plates for 16 hours at 37°
C to allow plaques to form . If mutagenesis is carried out by the Kunkel method ...
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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