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IRMM449

Genomic DNA of Escherichia coli O157 (EDL 933)

IRMM®, certified reference material

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About This Item

UNSPSC Code:
41116107
NACRES:
NA.24

grade

certified reference material

agency

IRMM®

manufacturer/tradename

JRC

application(s)

genomic analysis

format

neat

storage temp.

−20°C

General description

Certified for Genomic DNA Eschericha coli O157, strain EDL 933 confirmed by fliC gene.

IRMM-449_cert

IRMM-449_report

Analysis Note

For more information please see:
IRMM449

Legal Information

IRMM is a registered trademark of European Commission

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Berenice Talamantes-Becerra et al.
Journal of microbiological methods, 160, 11-19 (2019-03-22)
Bacterial identification methods used in routine identification of pathogens in medical microbiology include a combination approach of biochemical tests, mass spectrometry or molecular biology techniques. Extensive publicly-available databases of DNA sequence data from pathogenic bacteria have been amassed in recent
James F Parsons et al.
Acta crystallographica. Section D, Biological crystallography, 64(Pt 5), 607-610 (2008-05-06)
The electron carrier menaquinone is one of many important bacterial metabolites that are derived from the key intermediate chorismic acid. MenF, the first enzyme in the menaquinone pathway, catalyzes the isomerization of chorismate to isochorismate. Here, an improved structure of
Berenice Talamantes-Becerra et al.
BMC microbiology, 20(1), 114-114 (2020-05-15)
This study demonstrates the use of reduced-representation genotyping to provide preliminary identifications for thermophilic bacterial isolates. The approach combines restriction enzyme digestion and PCR with next-generation sequencing to provide thousands of short-read sequences from across the bacterial genomes. Isolates were
Bianca J Lam et al.
Nature biotechnology, 27(3), 288-292 (2009-02-24)
RNA enzymes have been developed that undergo self-sustained replication at a constant temperature in the absence of proteins. These RNA molecules amplify exponentially through a cross-replicative process, whereby two enzymes catalyze each other's synthesis by joining component oligonucleotides. Other RNA

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