B5926
10× REDTaq® PCR Reaction Buffer
To be used with REDTaq® DNA Polymerase
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About This Item
UNSPSC Code:
41106306
NACRES:
NA.52
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General description
10x REDTaq® PCR Reaction Buffer is a polymerase chain reaction buffer for use with REDTaq® DNA Polymerase (D4309).
Application
10× REDTaq® PCR Reaction Buffer has been used as a component of reaction mix:
- for PCR detection of virulence genes from Campylobacter jejuni food and clinical isolates in BALB/c mice
- for PCR detection of virulence genes of Campylobacter coli isolates from infected mice liver
- for identifying K-ras mutated alleles by PCR-restriction fragment length polymorphism (RFLP) in patients with colorectal carcinoma
Legal Information
REDTaq is a registered trademark of Merck KGaA, Darmstadt, Germany
Storage Class
12 - Non Combustible Liquids
wgk_germany
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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Christoph P Dieterle et al.
Clinical cancer research : an official journal of the American Association for Cancer Research, 10(2), 641-650 (2004-02-05)
The aim of this study was to identify K-ras mutations as marker for isolated tumor cells in liver, lymph node, and bone marrow specimens of colorectal cancer patients. To detect these, a PCR-RFLP assay was used with a sensitivity exceeding
Birte Meyer et al.
Microbiology (Reading, England), 153(Pt 7), 2026-2044 (2007-06-30)
Newly developed PCR assays were used to PCR-amplify and sequence fragments of the dissimilatory adenosine-5'-phosphosulfate (APS) reductase genes (aprBA) comprising nearly the entire gene locus (2.2-2.4 kb, equal to 92-94 % of the protein coding sequence) from 75 sulfate-reducing prokaryotes
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Erin M Symonds et al.
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Human fecal matter contains a large number of viruses, and current bacterial indicators used for monitoring water quality do not correlate with the presence of pathogenic viruses. Adenoviruses and enteroviruses have often been used to identify fecal pollution in the
Romain Marti et al.
Applied and environmental microbiology, 75(15), 4967-4974 (2009-06-16)
The objective of this study was to identify a microbial marker for pig manure contamination. We quantified the persistence of four dominant bacterial groups from the pig intestinal tract throughout manure handling at 10 livestock operations (including aerobic digestion) by
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