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cv b5 faulkner strain  (ATCC)


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    ATCC cv b5 faulkner strain
    Cv B5 Faulkner Strain, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 61 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cv+b5+faulkner+strain/Human+Coxsackievirus+B+5/pm41903231-71-7-11
    Average 94 stars, based on 61 article reviews
    cv b5 faulkner strain - by Bioz Stars, 2026-10
    94/100 stars

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    Article Title: Investigation of removal and inactivation efficiencies of human sapovirus in drinking water treatment processes by applying an in vitro cell-culture system.
    Article Snippet: Here, we examined the efficiencies of drinking water treatment processes for the removal and inactivation of human sapovirus (HuSaV).. We applied a recently developed in vitro cell-culture system to produce purified solutions of HuSaV containing virus concentrations high enough to conduct virus-spiking experiments, to develop an integrated cell culture-polymerase chain reaction (ICC-PCR) assay to quantify the infectivity of HuSaV, and to conduct virus-spiking experiments.. In virus-spiking coagulation-sedimentation–rapid sand filtration (CS–RSF) and coagulation–microfiltration (C–MF) experiments, HuSaV removals of 1.6–3.7-log10 and 1.2–>4.3-log10, respectively, were observed.

    Article Title: Evaluation of the suitability of a plant virus, pepper mild mottle virus, as a surrogate of human enteric viruses for assessment of the efficacy of coagulation-rapid sand filtration to remove those viruses.
    Article Snippet: AdV type 40 Dugan strain (ATCC VR-931), CV B5 Faulkner strain (ATCC VR-185), HAV IB HM175/18f strain (ATCC VR-1402), andMNV type 1 CW1 strain (ATCC PTA-5935) were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA) and propagated in human lung carcinoma epithelial cells (A549 cells; ATCC CCL-185, obtained from ATCC), buffalo green monkey kidney epithelial cells (BGM cells; kindly supplied by Dr. Daisuke Sano, Hokkaido University, Sapporo, Japan), fetal rhesus monkey kidney epithelial cells (FRhK-4 cells; ATCC CRL-1688, obtained from ATCC), and murine macrophage cells (RAW264.7 cells; ATCC TIB-71, obtained from ATCC), respectively.


    Article Title: Assessment of the efficacy of membrane filtration processes to remove human enteric viruses and the suitability of bacteriophages and a plant virus as surrogates for those viruses.
    Article Snippet: Here, we evaluated the efficacy of direct microfiltration (MF) and ultrafiltration (UF) to remove three representative human enteric viruses (i.e., adenovirus [AdV] type 40, coxsackievirus [CV] B5, and hepatitis A virus [HAV] IB), and one surrogate of human caliciviruses (i.e., murine norovirus [MNV] type 1).. Eight different MF membranes and three different UF membranes were used.. We also examined the ability of coagulation pretreatment with high-basicity polyaluminum chloride (PACl) to enhance virus removal by MF.



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