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african reen monkey kidney vero  (ATCC)


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    Structured Review

    ATCC african reen monkey kidney vero
    African Reen Monkey Kidney Vero, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 18063 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/monkey/Vero/pm42316883-220-43-48
    Average 99 stars, based on 18063 article reviews
    african reen monkey kidney vero - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Modification:

    Article Title: Plantaricin NC8 αβ rapidly and efficiently inhibits flaviviruses and SARS-CoV-2 by disrupting their envelopes
    Article Snippet: .. Monkey ( Cercopithecus aethiops ) epithelial kidney cells (Vero E6, ATCC, CRL-1586), dog ( Canis familiaris ) epithelial kidney cells (MDCK, ATCC, CCL-34), and human lung epithelial cells (A549, ATCC CCL-185) were maintained in Dulbecco’s Modified Eagle’s Medium (DMEM) containing 1 g/L glucose (Gibco), supplemented with 10% heat-inactivated fetal bovine serum (HI‒FBS, Gibco) and 100 U/mL penicillin-streptomycin (PEST, Gibco) at 37°C in 95% air and 5% CO 2 . .. Jurkat T-cells cells (ATCC, TIB-152) were maintained in RPMI 1640 medium (Fisher scientific, Austria) with 1.5 mM L -glutamine (Invitrogen, USA) and supplemented with 10% FBS.

    Article Title: Plantaricin NC8 αβ rapidly and efficiently inhibits flaviviruses and SARS-CoV-2 by disrupting their envelopes.
    Article Snippet: .. Monkey (Cercopithecus aethiops) epithelial kidney cells (Vero E6, ATCC, CRL-1586), dog (Canis familiaris) epithelial kidney cells (MDCK, ATCC, CCL-34), and human lung epithelial cells (A549, ATCC CCL-185) were maintained in Dulbecco’s Modified Eagle’s Medium (DMEM) containing 1 g/L glucose (Gibco), supplemented with 10% heat-inactivated fetal bovine serum (HI–FBS, Gibco) and 100 U/mL penicillin-streptomycin (PEST, Gibco) at 37 ̊C in 95% air and 5% CO2. .. Jurkat T-cells cells (ATCC, TIB-152) were maintained in RPMI 1640 medium (Fisher scientific, Austria) with 1.5 mM L-glutamine (Invitrogen, USA) and supplemented with 10% FBS.

    Cell Culture:

    Article Title: Furopyridine Derivatives as Potent Inhibitors of the Wild Type, L858R/T790M, and L858R/T790M/C797S EGFR.
    Article Snippet: The treatment of patients with nonsmall cell lung cancer (NSCLC) using epidermal growth factor receptor (EGFR) inhibitors is complicated by drug-sensitive activating L858R/ T790M and L858R/T790M/C797S mutations.. To overcome drug resistance, a series of furopyridine (PD) compounds were virtually screened to identify potent EGFR inhibitors using molecular docking and molecular dynamics (MD) simulations based on the solvated interaction energy (SIE) method.. Several PD compounds identified from virtual screening demonstrated the potential to suppress both wild-type and mutant forms of EGFR, with IC50 values in the nanomolar range.

    Article Title: Improved imaging and preservation of lysosome dynamics using silver nanoparticle-enhanced fluorescence
    Article Snippet: .. Cell culture, plasmids, and transfection The male-mouse macrophage-like RAW 264.7 cell line was obtained from ATCC (TIB-71, VA) and cultured in DMEM with 5% heat inactivated fetal bovine serum (FBS), reseeded every 2–3 d. The Cos7 cell line is a kidney-fibroblast-like cell derived from a male-green monkey and was obtained from ATCC (CRL-1651) and were cultured in DMEM with 10% FBS. .. Both cell types were plated at 30–50% confluency and used within 24–48 h. Plasmids were obtained from Addgene as follows: plasmid #34831 encoding LAMP1-GFP was a gift from Esteban Dell’ Angelica, plasmid #73080 encoding galectin3-GFP was a gift from Tamotsu Yoshimori, and plasmid #22418 encoding mCherry-GFP-LC3b was provided by Jayantha Debnath and previously characterized (Falcón-Pérez et al., 2005; N’Diaye et al., 2009; Maejima et al., 2013).

    Article Title: Furopyridine Derivatives as Potent Inhibitors of the Wild Type, L858R/T790M, and L858R/T790M/C797S EGFR
    Article Snippet: Poly(glu-tyr) peptide (P61–58) was purchased from SignalChem Biotech (Canada). .. The lung carcinoma A549 (ATCC CCL-185), H1975 (ATCC CRL-5908), and monkey ( Cercopithecus aethiopsis ) kidney Vero cell line (ATCC CCL-81) cell lines were purchased from the American Type Cell Culture Collection (ATCC, Manassas, VA). .. Dulbecco’s modified Eagle’s medium (DMEM), Roswell Park Memorial Institute (RPMI), fetal bovine serum (FBS), penicillin–streptomycin (Pen–Strep), and trypsin were purchased from Life Technologies (CA).

    Transfection:

    Article Title: Improved imaging and preservation of lysosome dynamics using silver nanoparticle-enhanced fluorescence
    Article Snippet: .. Cell culture, plasmids, and transfection The male-mouse macrophage-like RAW 264.7 cell line was obtained from ATCC (TIB-71, VA) and cultured in DMEM with 5% heat inactivated fetal bovine serum (FBS), reseeded every 2–3 d. The Cos7 cell line is a kidney-fibroblast-like cell derived from a male-green monkey and was obtained from ATCC (CRL-1651) and were cultured in DMEM with 10% FBS. .. Both cell types were plated at 30–50% confluency and used within 24–48 h. Plasmids were obtained from Addgene as follows: plasmid #34831 encoding LAMP1-GFP was a gift from Esteban Dell’ Angelica, plasmid #73080 encoding galectin3-GFP was a gift from Tamotsu Yoshimori, and plasmid #22418 encoding mCherry-GFP-LC3b was provided by Jayantha Debnath and previously characterized (Falcón-Pérez et al., 2005; N’Diaye et al., 2009; Maejima et al., 2013).

    Derivative Assay:

    Article Title: Improved imaging and preservation of lysosome dynamics using silver nanoparticle-enhanced fluorescence
    Article Snippet: .. Cell culture, plasmids, and transfection The male-mouse macrophage-like RAW 264.7 cell line was obtained from ATCC (TIB-71, VA) and cultured in DMEM with 5% heat inactivated fetal bovine serum (FBS), reseeded every 2–3 d. The Cos7 cell line is a kidney-fibroblast-like cell derived from a male-green monkey and was obtained from ATCC (CRL-1651) and were cultured in DMEM with 10% FBS. .. Both cell types were plated at 30–50% confluency and used within 24–48 h. Plasmids were obtained from Addgene as follows: plasmid #34831 encoding LAMP1-GFP was a gift from Esteban Dell’ Angelica, plasmid #73080 encoding galectin3-GFP was a gift from Tamotsu Yoshimori, and plasmid #22418 encoding mCherry-GFP-LC3b was provided by Jayantha Debnath and previously characterized (Falcón-Pérez et al., 2005; N’Diaye et al., 2009; Maejima et al., 2013).

    Incubation:

    Article Title: Exploring Synthetic Dihydrobenzofuran and Benzofuran Neolignans as Antiprotozoal Agents against Trypanosoma cruzi
    Article Snippet: .. Monkey ( Macaca mulata ) epithelial kidney cell line LLC-MK2 (ATCC ® CCL-7TM) was cultivated in RPMI 1640 medium (Roswell Park Memorial Institute; Gibco-Life Technology, Grand Island, NY, USA) supplemented with 10% fetal bovine serum (SFB) and antibiotics (penicillin: 10,000 UI/mL and streptomycin: 10,000 mg/mL) and incubated at 37 °C in a 5% CO 2 humidified incubator (Sanyo, Osaka, Japan) [ ]. .. The total spleen cell suspension was prepared using organs obtained from Swiss mice and macerated with RPMI 1640 medium (Gibco-Life Technology, Grand Island, NY, USA) in a Petri dish using a nylon sieve and a rubber stopper.

    other:

    Article Title: Discovery of JAK2/3 Inhibitors from Quinoxalinone-Containing Compounds
    Article Snippet: Human erythroleukemia TF1 (ATCC CRL-2003) and HEL 92.1.7 (ATCC TIB-180) cell lines, human liver cancer HepG2 cell line (ATCC HB-8065) and monkey ( Cercopithecus aethiops ) kidney Vero cell line (ATCC CCL-81) were purchased from American Type Culture Collection (ATCC, Manassas, VA, USA).



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    Intracochlear injection of SENS-501 in NHPs results in a mild humoral and an undetectable cellular response to the capsid (A) AAV8 anti-drug antibody (ADA) titers measured in serum at pre-dose and at 16, 29, and 92 days post-vector administration in NHPs. (B) Anti-AAV8 neutralizing antibodies (NAb) titers measured in serum at pre-dose and at 16, 29, and 92 days post-vector administration in NHPs. (C and D) <t>IFN-γ</t> spot forming units (SFUs) measured by ELISpot assay at 29 (C; left) and 92 (D; right) days post-injection. Peripheral blood mononuclear cells (PBMCs) from the indicated groups were stimulated with three different AAV8 peptide pools and a positive control (PMA/ionomycin). The dotted line represents the assay-specific positivity threshold. Each dot represents one animal. Bars represent the mean ± SEM.
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    ATCC african reen monkey kidney vero
    Intracochlear injection of SENS-501 in NHPs results in a mild humoral and an undetectable cellular response to the capsid (A) AAV8 anti-drug antibody (ADA) titers measured in serum at pre-dose and at 16, 29, and 92 days post-vector administration in NHPs. (B) Anti-AAV8 neutralizing antibodies (NAb) titers measured in serum at pre-dose and at 16, 29, and 92 days post-vector administration in NHPs. (C and D) <t>IFN-γ</t> spot forming units (SFUs) measured by ELISpot assay at 29 (C; left) and 92 (D; right) days post-injection. Peripheral blood mononuclear cells (PBMCs) from the indicated groups were stimulated with three different AAV8 peptide pools and a positive control (PMA/ionomycin). The dotted line represents the assay-specific positivity threshold. Each dot represents one animal. Bars represent the mean ± SEM.
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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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    ATCC african green monkey kidney fibroblast
    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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    ATCC african green monkey kidney cells
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    Image Search Results


    Intracochlear injection of SENS-501 in NHPs results in a mild humoral and an undetectable cellular response to the capsid (A) AAV8 anti-drug antibody (ADA) titers measured in serum at pre-dose and at 16, 29, and 92 days post-vector administration in NHPs. (B) Anti-AAV8 neutralizing antibodies (NAb) titers measured in serum at pre-dose and at 16, 29, and 92 days post-vector administration in NHPs. (C and D) IFN-γ spot forming units (SFUs) measured by ELISpot assay at 29 (C; left) and 92 (D; right) days post-injection. Peripheral blood mononuclear cells (PBMCs) from the indicated groups were stimulated with three different AAV8 peptide pools and a positive control (PMA/ionomycin). The dotted line represents the assay-specific positivity threshold. Each dot represents one animal. Bars represent the mean ± SEM.

    Journal: Molecular Therapy Advances

    Article Title: Efficacy and safety of SENS-501, a dual-AAV otoferlin gene therapy, for DFNB9 congenital deafness

    doi: 10.1016/j.omta.2026.201762

    Figure Lengend Snippet: Intracochlear injection of SENS-501 in NHPs results in a mild humoral and an undetectable cellular response to the capsid (A) AAV8 anti-drug antibody (ADA) titers measured in serum at pre-dose and at 16, 29, and 92 days post-vector administration in NHPs. (B) Anti-AAV8 neutralizing antibodies (NAb) titers measured in serum at pre-dose and at 16, 29, and 92 days post-vector administration in NHPs. (C and D) IFN-γ spot forming units (SFUs) measured by ELISpot assay at 29 (C; left) and 92 (D; right) days post-injection. Peripheral blood mononuclear cells (PBMCs) from the indicated groups were stimulated with three different AAV8 peptide pools and a positive control (PMA/ionomycin). The dotted line represents the assay-specific positivity threshold. Each dot represents one animal. Bars represent the mean ± SEM.

    Article Snippet: After the incubation, detection was performed with a monoclonal anti-monkey IFN-γ antibody (Monkey IFN-γ ELISpot Pro Kit, Mabtech) coupled with alkaline phosphatase and incubated with BCIP/NBT (5-bromo-4-chloro-3-indolyl-1-phosphate / nitroblue tetrazolium) substrate to detect secreted IFN-γ.

    Techniques: Injection, Plasmid Preparation, Enzyme-linked Immunospot, Positive Control

    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