TIANamp Virus DNA/RNA Kit

.. 835 / Publication

Column-based technology for virus DNA/RNA extraction from plasma, serum, and cell-free materials

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• StorageRoom temperature (15-25℃)
• DescriptionThe TIANamp Virus DNA/RNA Kit provides a fast, simple, and cost-effective method for virus DNA and RNA purification from plasma, serum and other cell-free samples. This kit is based on silica membrane technology and unique buffer system. Carrier RNA in this kit improves the binding of virus DNA/RNA to the silica membrane especially in the case of trace amount of samples. With no phenol/chloroform extraction, high-quality virus DNA/RNA is eluted in a small volume of RNase-Free ddH₂O. The purified DNA/RNA is ready for use in downstream applications such as PCR, restriction enzyme digestion, Southern blot, reverse transcription, etc.By applying this kit, high quality DNA/RNA could be purified from various virus samples including HBV, HPV, HCV and enterovirus within one hour.
• Required ReagentsEthanol
• Features■ High quality DNA/RNA can be purified within one hour.■ No need for phenol/chloroform extraction.■ High yield, excellent repeatability.■ Totally free from contaminants and inhibitors.

Publication

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Journals

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• Immunogenicity and protective efficacy of a novel bacterium-like particle-based vaccine displaying canine distemper virus antigens in mice and dogs.Microbiology spectrum2024-04-08 Read Article.. used for viral RNA extraction using the TIANamp Virus DNA/RNA Kit (Tiangen; Beijing; China).
• Analysis of Free Amino Acid Composition and Honey Plant Species in Seven Honey Species in ChinaFoods2024-03-29 Read Article.. plants; extracted DNA from plant leaf samples (Rapid DNA Extraction Kit; TIANGEN; Beijing; China); performed PCR and sequencing for
• The segmented flavivirus Alongshan virus reduces mitochondrial mass via degrading STAT2 to suppress innate immune responsebioRxiv2024-03-07 Read ArticlePrePrint: .. cell-culture supernatants using a viral RNA extraction kit (TIANGEN; Cat# DP315); and transcribed
• On-site detection and differentiation of African swine fever virus variants using an orthogonal CRISPR-Cas12b/Cas13a-based assayiScience2024-03-01 Read Article849 850 Nucleic acids of common swine pathogens were extracted using a TIANamp 851 virus DNA/RNA kit (TIANGEN; China).
• Rapid and sensitive detection of two fungal pathogens in soybeans using the recombinase polymerase amplification/CRISPR-Cas12a method for potential on-site disease diagnosis.Pest management science2024-02-08 Read ArticleAbstract: BACKGROUND: Diaporthe aspalathi and Diaporthe caulivora are two of the fungal pathogens causing soybean stem canker (SSC) in soybean; which is one of the most widespread diseases in soybean growing regions and can cause 100% loss of yield.. Current methods for the detection of fungal pathogens; including morphological identification and molecular detection; are mostly limited by the need for professional laboratories and staff.. To develop a detection method for potential on-site diagnosis for two of the fungal pathogens causing SSC; we designed a rapid assay combining recombinase polymerase amplification (RPA) and CRISPR-Cas12a-based diagnostics to specifically detect D. aspalathi and D. caulivora.
• TIANamp Virus DNA/RNA Kit
• E-mail: maggie@go2biotech.com / morgan@go2biotech.com
• Telephone:+86 755 8399 5017
• Address: Rm.1501 Grand Millennium Plaza (Lower Block),181
• Queen’s Road Central, Hong Kong