OPTIMASI DETEKSI GEN PADA Stelechocarpus burahol (Bl.) Hook.f. & Th. MENGGUNAKAN DIRECT KIR PCR
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AlShahni M.M., Makimura K, Yamada T., Satoh Y. (2009). Direct colony PCR of several medically important fungi using Ampdirect® Plus. Japanese Journal of Infectious Diseases.
Aziz SA and BC Ramadhan. 2013. Media and organic fertigation for growth and phytochemical properties of Stelechocarpus burahol in nursery. International Seminar Proceedings Forests & Medical Plants for Better Human Welfare. Bogor, 10-12 September 2013.Hlm. 200-204.
Bellstedt, D. U., Pirie, M. D., Visser, J. C., de Villiers, M. J., & Gehrke, B. (2010). A rapid and inexpensive method for the direct PCR amplification of DNA from plants. American Journal of Botany. https://doi.org/10.3732/ajb.1000181
Ben-Amar, A., Oueslati, S., & Mliki, A. (2017). Universal direct PCR amplification system: a time- and cost-effective tool for high-throughput applications. 3 Biotech. https://doi.org/10.1007/s13205-017-0890-7
Ben Amar, A., Oueslati, S., Ghorbel, A., & Mliki, A. (2012). Prediction and early detection of mycotoxigenic Fusarium culmorum in wheat by direct PCR-based procedure. Food Control. https://doi.org/10.1016/j.foodcont.2011.08.021
Berthomieu, P., & Meyer, C. (1991). Direct amplification of plant genomic DNA from leaf and root pieces using PCR. Plant Molecular Biology. https://doi.org/10.1007/BF00040656
Cao, M., Fu, Y., Guo, Y., & Pan, J. (2009). Chlamydomonas (Chlorophyceae) colony PCR. Protoplasma. https://doi.org/10.1007/s00709-009-0036-9
Cascella, R., Strafella, C., Ragazzo, M., Zampatti, S., Borgiani, P., Gambardella, S., Pirazzoli, A., Novelli, G., & Giardina, E. (2015). Direct PCR: A new pharmacogenetic approach for the inexpensive testing of HLA-B∗57:01. Pharmacogenomics Journal. https://doi.org/10.1038/tpj.2014.48
Chum, P. Y., Haimes, J. D., André, C. P., Kuusisto, P. K., & Kelley, M. L. (2012). Genotyping of plant and animal samples without prior DNA purification. Journal of Visualized Experiments. https://doi.org/10.3791/3844
Eszik, I., Lantos, I., Önder, K., Somogyvári, F., Burián, K., Endrész, V., & Virok, D. P. (2016). High dynamic range detection of Chlamydia trachomatis growth by direct quantitative PCR of the infected cells. Journal of Microbiological Methods. https://doi.org/10.1016/j.mimet.2015.11.010
Hwang, H., Bae, S.-C., Lee, S., Lee, Y.-H., & Chang, A. (2013). A Rapid and Simple Genotyping Method for Various Plants by Direct-PCR. Plant Breeding and Biotechnology, 1(3), 290–297. https://doi.org/10.9787/pbb.2013.1.3.29
John, M. E. (1992). An efficient method for isolation of RNA and DNA from plants containing polyphenolics. Nucleic Acids Research. https://doi.org/10.1093/nar/20.9.2381
Kim, C. S., Lee, C. H., Shin, J. S., Chung, Y. S., & Hyung, N. I. (1996). A simple and rapid method for isolation of high quality genomic DNA from fruit trees and conifers using PVP. Nucleic Acids Research. https://doi.org/10.1093/nar/25.5.1085
Klimyuk, V. I., Carroll, B. J., Thomas, C. M., & Jones, J. D. G. (1993). Alkali treatment for rapid preparation of plant material for reliable PCR analysis. The Plant Journal. https://doi.org/10.1111/j.1365-313X.1993.tb00169.x
Li, F. W., Kuo, L. Y., Huang, Y. M., Chiou, W. L., & Wang, C. N. (2010). Tissue-direct PCR, a rapid and extraction-free method for barcoding of ferns. Molecular Ecology Resources. https://doi.org/10.1111/j.1755-0998.2009.02745.x
Nishimura N, Nakayama T, Tonoike H, Kojima K, Kato S (2000) Direct polymerase chain reaction from whole blood without DNA isolation. Ann Clin Biochem 3
Pathmanathan SG, Cardona-Castro N, Sa´nchez-Jime´nez MM, CorreaOchoa MM, Puthucheary SD, Thong KL (2003) Simple and rapid detection of Salmonella strains by direct PCR amplification of the hilA gene. J Med Microbiol 52:773–778
Purwantiningsih, I Purwantini dan D Santoso. 2011. Identification of standard parameters of kepel leaves [Stelechocarpus burahol (Bl.) Hook. F. & Th.] and the extract as raw material for antihyperuricemic medicaments. Asian Journal of Pharmaceutical and Clinical Research 4(1): 149153.
Sharma, R., Kumar, V., Mohapatra, T., Khandelwal, V., & Vyas, G. K. (2012). A Simple and Non-destructive Method of Direct-PCR for Plant Systems. Journal of Plant Biology. https://doi.org/10.1007/s12374-011-9191-6
Shokralla, S., Singer, G. A. C., & Hajibabaei, M. (2010). Direct PCR amplification and sequencing of specimens’ DNA from preservative ethanol. BioTechniques. https://doi.org/10.2144/000113362
Surzycki, S., & Surzycki, S. (2000). Preparation of Genomic DNA from Plant Cells. In Basic Techniques in Molecular Biology. https://doi.org/10.1007/978-3-642-56968-5_3
Werblow, A., Flechl, E., Klimpel, S., Zittra, C., Lebl, K., Kieser, K., Laciny, A., Silbermayr, K., Melaun, C., & Fuehrer, H. P. (2016). Direct PCR of indigenous and invasive mosquito species: A time- and cost-effective technique of mosquito barcoding. Medical and Veterinary Entomology. https://doi.org/10.1111/mve.12154
White, T.J., Bruns, T., Lee, S.J.W.T., dan Taylor, J.W. 1990. Amplification and Direct Sequencing of Fungal Ribosomal RNA Genes for Pylogenetics. PCR Protocol: A Guide to Methods Application. 18:315-322.
Young, G. Y., Jong, Y. K., Soh, M. S., & Kim, D. S. (2007). A simple and rapid gene amplification from Arabidopsis leaves using AnyDirect system. Journal of Biochemistry and Molecular Biology. https://doi.org/10.5483/bmbrep.2007.40.3.444
DOI: https://doi.org/10.20886/jpth.2020.14.2.93-99
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