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african green monkey kidney vero 76 cells  (ATCC)


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    Structured Review

    ATCC african green monkey kidney vero 76 cells
    African Green Monkey Kidney Vero 76 Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1587 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/vero+african+green+monkey+kidney+cells/VERO+76/pm42882527-72-0-11
    Average 99 stars, based on 1587 article reviews
    african green monkey kidney vero 76 cells - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Modification:

    Article Title: Ecological vaccination: A strategy to prevent zoonotic spillover from bats.
    Article Snippet: .. Vero (African green monkey kidney) cells and human embryonic kidney (HEK) 293T cells were obtained from the American Type Culture Collection and maintained in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 8% fetal bovine serum (FBS), 1% l- glutamine, and 1% penicillin- streptomycin. ..

    other:

    Article Title: Comparative Evaluation of Carbohydrate, Amino Acid, and Ionic Liquid Excipients for Flavivirus Vaccine Stabilization
    Article Snippet: Vero African green monkey kidney cells from the American Type Culture Collection (Vero CCL-81, ATCC, Manassas, VA) were used as host/target cells for DENV-2, YFV-17D, and JEV in plaque forming unit titer assays.

    Article Title: Ecological vaccination: A strategy to prevent zoonotic spillover from bats
    Article Snippet: NiV infections were conducted in an ABSL-4 laboratory at Wuhan National Biosafety Laboratory (China Science and Technology Resource: 31120.02.NBL), Chinese Academy of Sciences.

    Incubation:

    Article Title: Computer-Aided Discovery of Small-Molecule Inhibitors of Pathogenic New World Arenavirus Entry and Replication.
    Article Snippet: A549 human epithelial lung cells (ATCC CCL-185) were treated with a 100 μL volumes of 4 log10 (100, 10, 1, 0.1 μM) or 8 half-log10 (100, 32, 10, 3.2, 1, 0.32, 0.1, 0.032 μM) dilutions of each analog, for 30 min in 96- well microplates before the addition of Candid#1 (multiplicity of infection/MOI = 0.01) in cell culture medium. .. Plates were incubated for 3 days and virus yields were determined by end point dilution of the culture supernatants on Vero African green monkey kidney cells (ATCC CCL-81). ..

    Virus:

    Article Title: Computer-Aided Discovery of Small-Molecule Inhibitors of Pathogenic New World Arenavirus Entry and Replication.
    Article Snippet: A549 human epithelial lung cells (ATCC CCL-185) were treated with a 100 μL volumes of 4 log10 (100, 10, 1, 0.1 μM) or 8 half-log10 (100, 32, 10, 3.2, 1, 0.32, 0.1, 0.032 μM) dilutions of each analog, for 30 min in 96- well microplates before the addition of Candid#1 (multiplicity of infection/MOI = 0.01) in cell culture medium. .. Plates were incubated for 3 days and virus yields were determined by end point dilution of the culture supernatants on Vero African green monkey kidney cells (ATCC CCL-81). ..

    Article Title: Herpes simplex virus type 1 R-loops are targets for APOBEC-mediated mutagenesis.
    Article Snippet: HEK293-AD pCMVA3A-tGFP and pCMVA3G-tGFP cells were established by stable transfection with APOBEC3A-tGFP and APOBEC3G-tGFP overexpression plasmids (OriGene, RG220995 and RG206821, respectively; pCMV6-AC-GFP backbone with C-terminal turboGFP tag and neomycin resistance) using PEI (25 kDa, branched; 100 μL of a 4.5 mg/10 mL stock) according to standard protocol. .. Vero African green monkey kidney cells (ATCC-CCL-81) were employed for virus propagation, AR TIC LE IN PR ES S maintained in Minimum Essential Medium. .. Vero African green monkey kidney cells (ATCC-CCL-81) were employed for virus propagation, AR TIC LE IN PR ES S maintained in Minimum Essential Medium.



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    ATCC african green monkey kidney vero cells
    Peptide from RNF213 truncation degrades ZIKV proteins and inhibits viral replication (A) The sequence of peptide from RNF213 truncation (PR-23) and control peptide. (B) A549 cells were infected with ZIKV (MOI = 0.01) and then treated with PR-23 (10 μM). Viral replication of cell supernatant was measured by plaque assay at 48 hpi. <t>(C–J)</t> <t>HEK293T</t> cells were treated with the indicated amount of PR-23 for 24 h, and then transfected with plasmids encoding HA-tagged ZIKV proteins. After 36 h, cell lysates were harvested and detected by western blot assay. GAPDH served as an internal control. (K) <t>Vero</t> cells were treated with the indicated dose of PR-23 for 6 h and transfected with the plasmid encoding GFP-tagged ZIKV E protein. After 36 h, the cells were fixed and subjected to immunofluorescence assay. The nucleus was stained with DAPI (blue). Images were obtained using a laser confocal microscope. Scale bars, 100 μm. Data are expressed as the mean ± SD from three independent experiments ( n = 3; ns, p > 0.05; ∗, p < 0.05; ∗∗∗, p < 0.001; ∗∗∗∗, p < 0.0001).
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    Image Search Results


    Peptide from RNF213 truncation degrades ZIKV proteins and inhibits viral replication (A) The sequence of peptide from RNF213 truncation (PR-23) and control peptide. (B) A549 cells were infected with ZIKV (MOI = 0.01) and then treated with PR-23 (10 μM). Viral replication of cell supernatant was measured by plaque assay at 48 hpi. (C–J) HEK293T cells were treated with the indicated amount of PR-23 for 24 h, and then transfected with plasmids encoding HA-tagged ZIKV proteins. After 36 h, cell lysates were harvested and detected by western blot assay. GAPDH served as an internal control. (K) Vero cells were treated with the indicated dose of PR-23 for 6 h and transfected with the plasmid encoding GFP-tagged ZIKV E protein. After 36 h, the cells were fixed and subjected to immunofluorescence assay. The nucleus was stained with DAPI (blue). Images were obtained using a laser confocal microscope. Scale bars, 100 μm. Data are expressed as the mean ± SD from three independent experiments ( n = 3; ns, p > 0.05; ∗, p < 0.05; ∗∗∗, p < 0.001; ∗∗∗∗, p < 0.0001).

    Journal: iScience

    Article Title: RNF213 isoform 2 restricts Zika virus through antiviral signaling and viral protein degradation

    doi: 10.1016/j.isci.2026.116284

    Figure Lengend Snippet: Peptide from RNF213 truncation degrades ZIKV proteins and inhibits viral replication (A) The sequence of peptide from RNF213 truncation (PR-23) and control peptide. (B) A549 cells were infected with ZIKV (MOI = 0.01) and then treated with PR-23 (10 μM). Viral replication of cell supernatant was measured by plaque assay at 48 hpi. (C–J) HEK293T cells were treated with the indicated amount of PR-23 for 24 h, and then transfected with plasmids encoding HA-tagged ZIKV proteins. After 36 h, cell lysates were harvested and detected by western blot assay. GAPDH served as an internal control. (K) Vero cells were treated with the indicated dose of PR-23 for 6 h and transfected with the plasmid encoding GFP-tagged ZIKV E protein. After 36 h, the cells were fixed and subjected to immunofluorescence assay. The nucleus was stained with DAPI (blue). Images were obtained using a laser confocal microscope. Scale bars, 100 μm. Data are expressed as the mean ± SD from three independent experiments ( n = 3; ns, p > 0.05; ∗, p < 0.05; ∗∗∗, p < 0.001; ∗∗∗∗, p < 0.0001).

    Article Snippet: Human embryonic kidney (HEK293T), human lung adenocarcinoma (A549), and African green monkey kidney (Vero) cells were purchased from the American Type Culture Collection (ATCC), IFNAR-knockout A549 cells were kindly provided by Prof. Genhong Cheng (Guangzhou National Laboratory).

    Techniques: Sequencing, Control, Infection, Plaque Assay, Transfection, Western Blot, Plasmid Preparation, Immunofluorescence, Staining, Microscopy