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Magmax for microarrays total rna isolation kit

Manufactured by Thermo Fisher Scientific
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The MagMAX for Microarrays Total RNA Isolation Kit is a product designed to extract total RNA from a variety of sample types. It utilizes magnetic bead-based technology to capture and purify the RNA, which can then be used for downstream applications such as microarray analysis.

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Lab products found in correlation

Rnaeasy kit, by Qiagen (4 mentions) Magna pure lc 2.0 or 96 systems, by Roche (2 mentions) Rnalater, by Thermo Fisher Scientific (2 mentions) Trioplex qrt pcr kit, by Thermo Fisher Scientific (2 mentions)

Close spelling variants of this product

MagMax Total RNA isolation kit RNA isolation kit

4 protocols using magmax for microarrays total rna isolation kit

1

Zika Virus Detection in Florida

Cited 1 time
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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 Surveillance in Miami-Dade Mosquitoes

Cited 1 time
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24,351 Ae. aegypti and Ae. albopictus mosquitoes (sorted into 2,596 pools) were collected throughout Miami-Dade County during June to November, 2016 using BG-Sentinel mosquito traps (Biogents AG). Up to 50 mosquitoes of the same species and sex were pooled per trap. The pooled mosquitoes were stored in RNAlater (Invitrogen), RNA was extracted using either the RNAeasy kit (QIAGEN) or MagMAX for Microarrays Total RNA Isolation Kit (Ambion), and ZIKV RNA was detected by qRT-PCR targeting the envelope protein coding region40 (link) or the Trioplex qRT-PCR kit41 (link). ZIKV infection rates were calculated per 1,000 female Ae. aegypti mosquitoes using the bias-corrected maximum likelihood estimate (MLE)42 . Days of insecticide usage by the Miami-Dade Mosquito Control were inferred from the zone-specific ZIKV activities timelines published by the Florida DOH35 .
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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3

Zika Virus Surveillance in Miami-Dade Mosquitoes

Cited 1 time
Check if the same lab product or an alternative is used in the 5 most similar protocols
24,351 Ae. aegypti and Ae. albopictus mosquitoes (sorted into 2,596 pools) were collected throughout Miami-Dade County during June to November, 2016 using BG-Sentinel mosquito traps (Biogents AG). Up to 50 mosquitoes of the same species and sex were pooled per trap. The pooled mosquitoes were stored in RNAlater (Invitrogen), RNA was extracted using either the RNAeasy kit (QIAGEN) or MagMAX for Microarrays Total RNA Isolation Kit (Ambion), and ZIKV RNA was detected by qRT-PCR targeting the envelope protein coding region40 (link) or the Trioplex qRT-PCR kit41 (link). ZIKV infection rates were calculated per 1,000 female Ae. aegypti mosquitoes using the bias-corrected maximum likelihood estimate (MLE)42 . Days of insecticide usage by the Miami-Dade Mosquito Control were inferred from the zone-specific ZIKV activities timelines published by the Florida DOH35 .
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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4

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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