Results 251 to 260 of about 1,136,601 (292)
Digital PCR Validation for Characterization of Quantitative Reference Material of Escherichia coli O157:H7 Genomic DNA. [PDF]
Methods ProtocTere-Peña CP +2 more
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Cultivation and Genomic DNA Extraction of Klebsiella pneumoniae. [PDF]
Curr ProtocPariseau DA, Ring BE, Khadka S, Mike LA.
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Method for isolation of high molecular weight genomic DNA from Botryococcus biomass. [PDF]
PLoS OneCornejo-Corona I +2 more
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RAD51 plays critical roles in DNMT1-mediated maintenance methylation of genomic DNA by dually regulating the ubiquitin ligase UHRF1. [PDF]
Proc Natl Acad Sci U S ALiu G +6 more
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T7 Endonuclease I-Mediated Single-Base Mismatch Biosensing Strategy for High-Resolution Quantitative Analysis of 5-Hydroxymethylcytosine in Genomic DNA. [PDF]
JACS AuZhao Z +8 more
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Preparing Bacterial Genomic DNA
Cold Spring Harbor Protocols, 2022We describe two alternative procedures for purifying bacterial chromosomal DNA. The first procedure incorporates the use of a commercial kit based on silica membrane technology. This approach relies on the selective binding of DNA to a silica-based column in the presence of chaotropic salts (guanidine salts).
Nara Figueroa-Bossi +2 more
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Current Biology, 1994
The extremely high AT content of bat DNA complicates the reconstruction of bat phylogeny from DNA sequence data, but may help throw light on genomic evolution.
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The extremely high AT content of bat DNA complicates the reconstruction of bat phylogeny from DNA sequence data, but may help throw light on genomic evolution.
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Current Protocols in Molecular Biology, 1987
AbstractGenomic DNA libraries are almost always screened by hybridization using a radioactive nucleic acid probe. Since this approach is essentially independent of a particular vector or type of target DNA, the main problem faced when considering creation of a genomic DNA library is simply generating a large enough number of recombinant DNA clones. The
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AbstractGenomic DNA libraries are almost always screened by hybridization using a radioactive nucleic acid probe. Since this approach is essentially independent of a particular vector or type of target DNA, the main problem faced when considering creation of a genomic DNA library is simply generating a large enough number of recombinant DNA clones. The
openaire +2 more sources