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Cpxv brighton red

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The CPXV Brighton Red is a laboratory equipment product. It serves as a core function to perform tasks related to the analysis and study of samples.

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Lab products found in correlation

Vero cell, by American Type Culture Collection (2 mentions) Vero e6 cell, by American Type Culture Collection (2 mentions) Bsc 40 cells, by American Type Culture Collection (2 mentions)

2 protocols using cpxv brighton red

1

Propagation and Titration of Orthopoxviruses

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VACV Dryvax (NIH, Lot# 4008284), VACV Western Reserve (VACV-WR; ATCC VR-119) and CPXV Brighton Red (BEI Resources, NR-88) were propagated and titered in monolayer cultures of BSC-40 cells (ATCC CRL-2761). MPXV Zaire was propagated in BSC-40 cells and titered on Vero cells (ATCC CCL-81). Bangladesh 1974 Solaiman strain of VARV was propagated in monolayer cultures of Vero E6 cells (ATCC CRL-1586). VACV and CPXV were manipulated under BSL-2 conditions by vaccinated personnel. MPXV was manipulated under BSL-2 conditions with BSL-3 precautions by vaccinated personnel. All experiments with live VARV were reviewed and approved by the World Health Organization Advisory Committee on Variola Virus Research (WHO ACVVR). Experiments with VARV were conducted in accordance with WHO ACVVR guidelines and within a biosafety level 4 laboratory.
Gilchuk I., Gilchuk P., Sapparapu G., Lampley R., Singh V., Kose N., Blum D.L., Hughes L.J., Satheshkumar P.S., Townsend M.B., Kondas A.V., Reed Z., Weiner Z., Olson V.A., Hammarlund E., Raue H.P., Slifka M.K., Slaughter J.C., Graham B.S., Edwards K.M., Eisenberg R.J., Cohen G.H., Joyce S, & Crowe JE J.r. (2016). Cross-Neutralizing and Protective Human Antibody Specificities to Poxvirus Infections. Cell, 167(3), 684-694.e9.
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2

Propagation and Titration of Orthopoxviruses

Check if the same lab product or an alternative is used in the 5 most similar protocols
VACV Dryvax (NIH, Lot# 4008284), VACV Western Reserve (VACV-WR; ATCC VR-119) and CPXV Brighton Red (BEI Resources, NR-88) were propagated and titered in monolayer cultures of BSC-40 cells (ATCC CRL-2761). MPXV Zaire was propagated in BSC-40 cells and titered on Vero cells (ATCC CCL-81). Bangladesh 1974 Solaiman strain of VARV was propagated in monolayer cultures of Vero E6 cells (ATCC CRL-1586). VACV and CPXV were manipulated under BSL-2 conditions by vaccinated personnel. MPXV was manipulated under BSL-2 conditions with BSL-3 precautions by vaccinated personnel. All experiments with live VARV were reviewed and approved by the World Health Organization Advisory Committee on Variola Virus Research (WHO ACVVR). Experiments with VARV were conducted in accordance with WHO ACVVR guidelines and within a biosafety level 4 laboratory.
Gilchuk I., Gilchuk P., Sapparapu G., Lampley R., Singh V., Kose N., Blum D.L., Hughes L.J., Satheshkumar P.S., Townsend M.B., Kondas A.V., Reed Z., Weiner Z., Olson V.A., Hammarlund E., Raue H.P., Slifka M.K., Slaughter J.C., Graham B.S., Edwards K.M., Eisenberg R.J., Cohen G.H., Joyce S, & Crowe JE J.r. (2016). Cross-Neutralizing and Protective Human Antibody Specificities to Poxvirus Infections. Cell, 167(3), 684-694.e9.
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