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一般說明
10x REDTaq® PCR Reaction Buffer is a polymerase chain reaction buffer for use with REDTaq® DNA Polymerase (D4309).
應用
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
法律資訊
REDTaq is a registered trademark of Merck KGaA, Darmstadt, Germany
儲存類別代碼
10 - Combustible liquids
水污染物質分類(WGK)
WGK 1
閃點(°F)
Not applicable
閃點(°C)
Not applicable
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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
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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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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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