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Magna pure lc 2.0 or 96 systems

Manufactured by Roche
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The MagNA Pure LC 2.0 or 96 Systems are automated nucleic acid extraction and purification platforms developed by Roche. These systems utilize magnetic bead-based technology to extract and purify DNA, RNA, and other nucleic acids from a variety of sample types. The core function of these systems is to provide a reliable and standardized method for obtaining high-quality nucleic acid samples that can be used in downstream applications such as PCR, sequencing, and other analyses.

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Lab products found in correlation

Rnaeasy kit, by Qiagen (2 mentions) Magmax for microarrays total rna isolation kit, by Thermo Fisher Scientific (2 mentions)

Close spelling variants of this product

MagNA Pure LC 2.0 system MagNA Pure LC system MagNA Pure LC 2.0 MagNA Pure system MagNA Pure LC MagNA Pure 96 MagNA Pure

2 protocols using magna pure lc 2.0 or 96 systems

1

Zika Virus Detection in Florida

Cited 1 time
Check if the same lab product or an alternative is used in the 5 most similar protocols
Clinical samples from locally-acquired ZIKV infections were collected from June 22 to October 11, 2016. The Florida DOH identified persons with compatible illness and clinical samples were shipped to the Bureau of Public Health Laboratories for confirmation by qRT-PCR and antibody tests following interim guidelines3 (link),38 (link)–40 (link). Clinical specimens (whole blood, serum, saliva, or urine) submitted for analysis were refrigerated or frozen at ≤ −70°C until RNA was extracted. RNA was extracted using the RNAeasy kit (QIAGEN), MagMAX for Microarrays Total RNA Isolation Kit (Ambion), or MagNA Pure LC 2.0 or 96 Systems (Roche Diagnostics). Purified RNA was eluted into 50–100 μL using the supplied elution buffers, immediately frozen at ≤ −70°C, and transported on dry ice. The Florida DOH also provided investigation data for these samples, including symptom onset dates and, when available, assignments to the zone where infection likely occurred (Supplementary Table 1).
Grubaugh N.D., Ladner J.T., Kraemer M.U., Dudas G., Tan A.L., Gangavarapu K., Wiley M.R., White S., Thézé J., Magnani D.M., Prieto K., Reyes D., Bingham A., Paul L.M., Robles-Sikisaka R., Oliveira G., Pronty D., Barcellona C.M., Metsky H.C., Baniecki M.L., Barnes K.G., Chak B., Freije C.A., Gladden-Young A., Gnirke A., Luo C., MacInnis B., Matranga C.B., Park D.J., Qu J., Schaffner S.F., Tomkins-Tinch C., West K.L., Winnicki S.M., Wohl S., Yozwiak N.L., Quick J., Fauver J.R., Khan K., Brent S.E., Reiner RC J.r., Lichtenberger P.N., Ricciardi M., Bailey V.K., Watkins D.I., Cone M.R., Kopp EW I.V., Hogan K.N., Cannons A.C., Jean R., Monaghan A.J., Garry R.F., Loman N.J., Faria N.R., Porcelli M.C., Vasquez C., Nagle E.R., Cummings D.A., Stanek D., Rambaut A., Sanchez-Lockhart M., Sabeti P.C., Gillis L.D., Michael S.F., Bedford T., Pybus O.G., Isern S., Palacios G, & Andersen K.G. (2017). Genomic epidemiology reveals multiple introductions of Zika virus into the United States. Nature, 546(7658), 401-405.
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2

Zika Virus Detection in Florida

Cited 1 time
Check if the same lab product or an alternative is used in the 5 most similar protocols
Clinical samples from locally-acquired ZIKV infections were collected from June 22 to October 11, 2016. The Florida DOH identified persons with compatible illness and clinical samples were shipped to the Bureau of Public Health Laboratories for confirmation by qRT-PCR and antibody tests following interim guidelines3 (link),38 (link)–40 (link). Clinical specimens (whole blood, serum, saliva, or urine) submitted for analysis were refrigerated or frozen at ≤ −70°C until RNA was extracted. RNA was extracted using the RNAeasy kit (QIAGEN), MagMAX for Microarrays Total RNA Isolation Kit (Ambion), or MagNA Pure LC 2.0 or 96 Systems (Roche Diagnostics). Purified RNA was eluted into 50–100 μL using the supplied elution buffers, immediately frozen at ≤ −70°C, and transported on dry ice. The Florida DOH also provided investigation data for these samples, including symptom onset dates and, when available, assignments to the zone where infection likely occurred (Supplementary Table 1).
Grubaugh N.D., Ladner J.T., Kraemer M.U., Dudas G., Tan A.L., Gangavarapu K., Wiley M.R., White S., Thézé J., Magnani D.M., Prieto K., Reyes D., Bingham A., Paul L.M., Robles-Sikisaka R., Oliveira G., Pronty D., Barcellona C.M., Metsky H.C., Baniecki M.L., Barnes K.G., Chak B., Freije C.A., Gladden-Young A., Gnirke A., Luo C., MacInnis B., Matranga C.B., Park D.J., Qu J., Schaffner S.F., Tomkins-Tinch C., West K.L., Winnicki S.M., Wohl S., Yozwiak N.L., Quick J., Fauver J.R., Khan K., Brent S.E., Reiner RC J.r., Lichtenberger P.N., Ricciardi M., Bailey V.K., Watkins D.I., Cone M.R., Kopp EW I.V., Hogan K.N., Cannons A.C., Jean R., Monaghan A.J., Garry R.F., Loman N.J., Faria N.R., Porcelli M.C., Vasquez C., Nagle E.R., Cummings D.A., Stanek D., Rambaut A., Sanchez-Lockhart M., Sabeti P.C., Gillis L.D., Michael S.F., Bedford T., Pybus O.G., Isern S., Palacios G, & Andersen K.G. (2017). Genomic epidemiology reveals multiple introductions of Zika virus into the United States. Nature, 546(7658), 401-405.
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