Molecular Cloning: A Laboratory Manual, Book 2 |
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Results 1-3 of 9
Page 9-38
2 N HCl and then rinse briefly with deionized water . 3 . Rinse the gel briefly in
deionized water , and then neutralize it by soaking for 30 minutes in several
volumes of a solution of 1 m Tris ( pH 7 . 4 ) , 1 . 5 m NaCl at room temperature
with ...
2 N HCl and then rinse briefly with deionized water . 3 . Rinse the gel briefly in
deionized water , and then neutralize it by soaking for 30 minutes in several
volumes of a solution of 1 m Tris ( pH 7 . 4 ) , 1 . 5 m NaCl at room temperature
with ...
Page 9-45
2 N HCl and then rinse briefly with deionized water . 3 . While the gel is soaking
in the denaturation / transfer solution , prepare the nylon membrane as follows : a
. Using a fresh scalpel or a paper cutter , cut a piece of membrane about 1 mm ...
2 N HCl and then rinse briefly with deionized water . 3 . While the gel is soaking
in the denaturation / transfer solution , prepare the nylon membrane as follows : a
. Using a fresh scalpel or a paper cutter , cut a piece of membrane about 1 mm ...
Page 11-24
Caution : Handle the KOH and the KOH / methanol solutions with great care . Use
gloves and a face protector . Then wash the glass plates and spacers in warm
detergent solution and rinse thoroughly in tap water , followed by deionized water
...
Caution : Handle the KOH and the KOH / methanol solutions with great care . Use
gloves and a face protector . Then wash the glass plates and spacers in warm
detergent solution and rinse thoroughly in tap water , followed by deionized water
...
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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
DNA METHYLATION 5 | 8-5 |
SOLUTIONS FOR WORKING WITH BACTERIOPHAGEI A | 8-7 |
SYNTHESIS OF THE FIRST STRAND OF DNA 8 | 8-11 |
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Common terms and phrases
aliquots allow amount amplification antibody appropriate approximately bacteriophage bacteriophage T4 base binding buffer carried cDNA cells centrifugation Chapter chromatography cleaved clones colonies complete concentration constructed containing deletions denatured described detection determine digestion dNTPs double-stranded efficiency electrophoresis et al ethanol expression extraction Figure filters four fragment gene genomic DNA hybridization increase Incubate inserted interest isolation Klenow labeled length libraries ligation linear linkers membrane method minutes mixture molecules mRNA mutants nucleic acids nucleotides obtained oligonucleotide plaques plasmid DNA plate position possible precipitation prepared presence primer probe problem protein purified radioactivity radiolabeled reaction recombinant region remove restriction enzyme room temperature samples screening separate sequence single single-stranded solution step stored strand synthesis target DNA target sequence template termini transfer Tris tube units usually vectors volume