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Merck

B5926

Sigma-Aldrich

10× REDTaq® PCR Reaction Buffer

To be used with REDTaq® DNA Polymerase

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About This Item

Kod UNSPSC:
41106306
NACRES:
NA.52

Poziom jakości

Postać

liquid

kolor

colorless

temp. przechowywania

−20°C

Opis ogólny

10x REDTaq® PCR Reaction Buffer is a polymerase chain reaction buffer for use with REDTaq® DNA Polymerase (D4309).

Zastosowanie

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

Informacje prawne

REDTaq is a registered trademark of Merck KGaA, Darmstadt, Germany
This page may contain text that has been machine translated.

Kod klasy składowania

12 - Non Combustible Liquids

Klasa zagrożenia wodnego (WGK)

WGK 1

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable


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Odwiedź Bibliotekę dokumentów

Ovidiu Paun et al.
Molecular biology and evolution, 27(11), 2465-2473 (2010-06-17)
Epigenetic information includes heritable signals that modulate gene expression but are not encoded in the primary nucleotide sequence. We have studied natural epigenetic variation in three allotetraploid sibling orchid species (Dactylorhiza majalis s.str, D. traunsteineri s.l., and D. ebudensis) that
Chris Waskewich et al.
Cancer research, 62(7), 2029-2033 (2002-04-04)
Cyclooxygenase-2 (COX-2) is an important cellular target for both therapy and/or prevention of inflammatory disorders and cancer. The advent of selective COX-2 inhibitors now allows a more precise and safer treatment approach. The screening of an array of cancer cell
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
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
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

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