一般描述
10x REDTaq® PCR Reaction Buffer is a polymerase chain reaction buffer for use with REDTaq® DNA Polymerase (D4309).
应用
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
法律信息
REDTaq is a registered trademark of Merck KGaA, Darmstadt, Germany
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
Virulence comparison of human and poultry campylobacter Jejuni isolates in a mouse model
Vuvckovic D, et al.
Medical Research Engineering, 5(10) (2017)
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
Kimberly P Tucker et al.
The ISME journal, 5(5), 822-830 (2010-12-03)
Knowledge of marine phages is highly biased toward double-stranded DNA (dsDNA) phages; however, recent metagenomic surveys have also identified single-stranded DNA (ssDNA) phages in the oceans. Here, we describe two complete ssDNA phage genomes that were reconstructed from a viral
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
Erin M Symonds et al.
Applied and environmental microbiology, 75(5), 1402-1409 (2009-01-07)
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
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