Description
The GF-1 Viral Nucleic Acid Extraction Kit is designed for rapid and efficient purification of viral DNA/RNA from samples such as serum, plasma, body fluid or virus-infected cell culture supernatant. The purification is based on the usage of denaturing agents to provide efficient cell lysis, denaturation of proteins and subsequent release of DNA or RNA. Special buffers provided in the kit are optimized to enhance the binding of DNA or RNA onto a specially-treated glass filter membrane for efficient recovery of highly pure DNA or RNA.
Features
- No organic-based extraction required.
- Highly pure DNA or RNA, ready to use for routine molecular biology applications such as PCR and RT-PCR.
Kit Components
- Buffer VL
- Wash Buffer 1 (concentrate)
- Wash Buffer 2 (concentrate)
- Elution Buffer (concentrate)
- Proteinase K (concentrate)
Ordering Information
| Catalog No | Description | Pack Size |
| GF-RD-025 | GF-1 Viral Nucleic Acid Extraction Kit | 25 preps |
| GF-RD-050 | GF-1 Viral Nucleic Acid Extraction Kit | 50 preps |
| GF-RD-100 | GF-1 Viral Nucleic Acid Extraction Kit | 100 preps |
| GF-RD-300 | GF-1 Viral Nucleic Acid Extraction Kit | 300 preps |
Download
Manual
GF-1 Viral Nucleic Acid Extraction Kit
Download
MSDS
GF-1 Viral Nucleic Acid Extraction Kit
Stability Test Report
Application Note
Publication
This Product Has Been Used In:
Atasoy M O et al. (2022) Genetic diversity, frequency and concurrent infections of picobirnaviruses in diarrhoeic calves in Turkey, Tropical Animal Health and Production , 54:127
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Ahmed et al. (2020) Enhanced Efficacy of Direct-Acting Antivirals in Hepatitis C Patients by Coadministration of Black Cumin and Ascorbate as Antioxidant Adjuvants, Oxidative Medicine and Cellular Longevity, Volume 2020, Article ID 7087921.
Azad, A.R. et al. (2020) The Prevalence of Hepatitis B and D Viruses and Evaluating YMDD Mutation in HBV-Suspected Patients in Qom Province, Iran, Jundishapur Journal of Microbiology, 13(2):e100038.
Khaliq SA et al. (2020). Clinico-Hemato-Biochemical and Molecular Diagnostic Investigations of Peste des Petits Ruminants in Goats, . Pakistan Veterinary Journal, 2074-7764.
Ayse Erdem Yayla et al. (2019) Investigation of Human Papillomavirus Prevalence in Married Women and and Molecular Characterization and Phylogenetic Analysis of the Virus, . Obstetrics and Gynecology Science 62(4):264-272.
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MO Timurkan et al. (2019) Identification and molecular characterization of bovine parainfluenza virus-3 and bovine respiratory syncytial virus – first report from Turkey. Journal of Veterinary Research 63:167-173.
Liamnimitr, P. et al. (2018) Non-lethal sampling for Tilapia Lake Virus detection by RT-qPCR and cell culture,. Aquaculture, 75-80.
N.E. Sainei, V.S. Kumar, Y.S. Chin & F.A.M. Salih (2018) High Prevalence of Human Papillomavirus Types 56 and 70 Identified in the Native Populations of Sabah, Malaysia, . Asian Pacific Journal of Cancer Prevention, 19(10):2807-2813.
Turan, T. et al. (2018) Detection and molecular analysis of bovine enteric norovirus and nebovirus in Turkey, Journal of Veterinary Research, 62:129-135.
Zainathan, S.C., Johan, C.A.C., Subramaniam, N., Ahmad, A.A., Halim, N.I.A., Norizan, N.,Ariff, N. (2017). Detection and molecular characterization of Megalocytivirus strain ISKNV in freshwater ornamental fish from Southern Malaysia . , AACL Bioflux Vol. 10, No. 5 (2017).
Majid Rahmati et al. (2016) Cloning and expression of human bone morphogenetic protein-2 gene in Leishmania tarentolae, Biocatalysis and Agricultural Biotechnology https://doi.org/10.1016/j.bcab.2016.01.006.Volume 5, 2016, Pages 199-203, ISSN 1878-8181
Khalafalla, A.I., Al-Busada, K.A., & El-Sabagh, I.M. (2015) Multiplex PCR for Rapid Diagnosis and Differentiation of Pox and Pox-like Diseases in Dromedary Camels. Virology Journal. 12(102), p. 1-10.
Nikoozad, R., Mahzounieh, M.R., & Ghorani, M.R. (2015) Detection of Parvovirus B19 Infection in Thalasemic Patients in Isfahan Province, Iran. Jundishapur Journal of Microbiology. 8(11).
Sasithorn Uttatreea, Jittima Charoenpanich (2015). Isolation and Characterization of a Broad Range pH and Temperature Active Protease from Staphylococcus saprophyticus. Burapha University International Conference 2015
Habib, M., Shah, M.S., Muzammil, H.M., Manzoor, S., Khan, R.S.A., Munir, R., Rajput, Z.I., Farooq, U. (2014). Investigations of Foot-and-Mouth Disease Outbreaks in Faisalabad District of Punjab, Pakistan during the Year 2013, Pakistan Journal of Life and Social Sciences, Vol. 12, No. 3, 165-159 (2014).
Fatima, Z., et. al (2013) Change in Demographic Pattern of Dengue Virus Infection: Evidence from 2011 Dengue Outbreak in Punjab, Pakistan Public Health
Hussain, A. and Idrees, M. (2013) The First Complete Genome Sequence of HCV-1a from Pakistan and a Phylogenetic Analysis with Complete Genomes from the Rest of the World. Virol J.;10: 211.
Hohmann, H., Lamoller, L., Klein-Unseld, R., Maxeiner, H.G., Bechter, K., Schneider, M. (2012) Classification of free nucleic acids in cerebrospinal fluid of psychiatric patients. Neurology, Psychiatry and Brain Research. 18 (2) pp.60
Charoenpanich, Jittima et al. (2011). Production of a thermostable lipase by Aeromonas sp. EBB1 isolated from marine sludge in Angsila, Thailand. ScienceAsia. 37. 105-114. 10.2306/scienceasia1513-1874.2011.37.105.
A.Y. Joseph et al. (2008) Rapid detection and characterization of Chikungunya virus by RT-PCR in febrile patients from Kerala India,. Indian Journal of Experimental Biology, 46:573-578.
