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rhesus macaque epithelial cells llc mk2  (ATCC)


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    Structured Review

    ATCC rhesus macaque epithelial cells llc mk2
    Rhesus Macaque Epithelial Cells Llc Mk2, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 918 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/llc+mk2/LLC-MK2+Original/pm42274213-350-71-92
    Average 99 stars, based on 918 article reviews
    rhesus macaque epithelial cells llc mk2 - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Virus:

    Article Title: N4-hydroxycytidine and derivatives and anti-viral uses related thereto
    Article Snippet: Virus Preparation—The Dengue virus type 2 New Guinea C strain was obtained from ATCC (catalog #VR-1584) and was grown in LLC-MK2 (Rhesus monkey kidney cells; catalog #CCL-7.1) cells for the production of stock virus pools. .. Virus Preparation—The Dengue virus type 2 New Guinea C strain was obtained from ATCC (catalog #VR-1584) and was grown in LLC-MK2 (Rhesus monkey kidney cells; catalog #CCL-7.1) cells for the production of stock virus pools. ..

    other:

    Article Title: Chlorinated bis-4-hydroxycoumarins suppress flavivirus replication by inhibiting dengue virus type 2 translation and replication
    Article Snippet: Vero (ATCC ® CCL-81), LLC/MK2 (ATCC ® CCL-7), C6/36 (ATCC ® CRL-1660), HepG2 (ATCC ® HB-8065), HEK-293 (ATCC ® CRL-1573) and A549 (ATCC ® CCL-185) cells were maintained as previously described – .

    Article Title: Experimental inoculation of pigs with porcine parainfluenza virus 1 revealed pathological manifestations in the upper respiratory tract
    Article Snippet: Two cell lines, LLC-MK2 (ATCC, CCL-7) and Calu-3 (ATCC, HTB-55) were maintained at 37 °C in a humidified 5% CO 2 incubator and grown in cultivation media consisting of Eagle’s Minimal Essential Media (MEM) (Gibco, Thermo Fisher Scientific, Waltham, MA, USA) supplemented with 100 U/ml penicillin-streptomycin (Invitrogen, Thermo Fisher Scientific), 2mM L-Glutamine (Sigma-Aldrich, St. Louis, MO, USA), and 10% fetal bovine serum (Gibco).

    Derivative Assay:

    Article Title: 2-Aminothiophene Derivative SB-83 Inhibits Trypanothione Reductase and Modulates Cytokine Production in Trypanosoma cruzi -Infected Cells
    Article Snippet: .. LLC-MK2 (ATCC CCL-7) cell lines derived from rhesus monkey kidney, Vero (ATCC CCL-81) cell lines derived from African green monkey kidney, and RAW 264.7 macrophages (ATCC TIB-7) were cultured in DMEM, supplemented with 10% FBS and 1% antibiotic solution. ..

    Article Title: 2-Aminothiophene Derivative SB-83 Inhibits Trypanothione Reductase and Modulates Cytokine Production in Trypanosoma cruzi -Infected Cells.
    Article Snippet: .. LLC-MK2 (ATCC CCL-7) cell lines derived from rhesus monkey kidney, Vero (ATCC CCL-81) cell lines derived from African green monkey kidney, and RAW 264.7 macrophages (ATCC TIB-7) were cultured in DMEM, supplemented with 10% FBS and 1% antibiotic solution. ..

    Cell Culture:

    Article Title: 2-Aminothiophene Derivative SB-83 Inhibits Trypanothione Reductase and Modulates Cytokine Production in Trypanosoma cruzi -Infected Cells
    Article Snippet: .. LLC-MK2 (ATCC CCL-7) cell lines derived from rhesus monkey kidney, Vero (ATCC CCL-81) cell lines derived from African green monkey kidney, and RAW 264.7 macrophages (ATCC TIB-7) were cultured in DMEM, supplemented with 10% FBS and 1% antibiotic solution. ..

    Article Title: 2-Aminothiophene Derivative SB-83 Inhibits Trypanothione Reductase and Modulates Cytokine Production in Trypanosoma cruzi -Infected Cells.
    Article Snippet: .. LLC-MK2 (ATCC CCL-7) cell lines derived from rhesus monkey kidney, Vero (ATCC CCL-81) cell lines derived from African green monkey kidney, and RAW 264.7 macrophages (ATCC TIB-7) were cultured in DMEM, supplemented with 10% FBS and 1% antibiotic solution. ..



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    Differential IRGs and ISGs expressed during hMPV infection. A Heatmap of differentially expressed IRGs and ISGs with P values of < 0.05 in the hMPV group versus the control group and the RSV group. B Detailed expression levels of IRGs and ISGs with P values < 0.05 in the three groups. Statistical analysis was performed with an unpaired t -test. P values of 0.05 (∗), 0.01 (∗∗), and 0.001 (∗∗∗) were considered significant; NS: not significant. C Real-time PCR quantification of selected IRGs in infected and control cells at 24, 48, and 72 h postinfection. RSV and hMPV were propagated <t>in</t> <t>LLC-MK2</t> cells at a multiplicity of infection (MOI) of 0.1. N = 3. Statistical analysis was performed with an unpaired t -test. P values < 0.05 (∗), < 0.01 (∗∗), and < 0.0001 (∗∗∗∗) were considered significant. The bars in the figure panels show the means and standard errors of the means (SEMs).
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    Differential IRGs and ISGs expressed during hMPV infection. A Heatmap of differentially expressed IRGs and ISGs with P values of < 0.05 in the hMPV group versus the control group and the RSV group. B Detailed expression levels of IRGs and ISGs with P values < 0.05 in the three groups. Statistical analysis was performed with an unpaired t -test. P values of 0.05 (∗), 0.01 (∗∗), and 0.001 (∗∗∗) were considered significant; NS: not significant. C Real-time PCR quantification of selected IRGs in infected and control cells at 24, 48, and 72 h postinfection. RSV and hMPV were propagated <t>in</t> <t>LLC-MK2</t> cells at a multiplicity of infection (MOI) of 0.1. N = 3. Statistical analysis was performed with an unpaired t -test. P values < 0.05 (∗), < 0.01 (∗∗), and < 0.0001 (∗∗∗∗) were considered significant. The bars in the figure panels show the means and standard errors of the means (SEMs).
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    Differential IRGs and ISGs expressed during hMPV infection. A Heatmap of differentially expressed IRGs and ISGs with P values of < 0.05 in the hMPV group versus the control group and the RSV group. B Detailed expression levels of IRGs and ISGs with P values < 0.05 in the three groups. Statistical analysis was performed with an unpaired t -test. P values of 0.05 (∗), 0.01 (∗∗), and 0.001 (∗∗∗) were considered significant; NS: not significant. C Real-time PCR quantification of selected IRGs in infected and control cells at 24, 48, and 72 h postinfection. RSV and hMPV were propagated <t>in</t> <t>LLC-MK2</t> cells at a multiplicity of infection (MOI) of 0.1. N = 3. Statistical analysis was performed with an unpaired t -test. P values < 0.05 (∗), < 0.01 (∗∗), and < 0.0001 (∗∗∗∗) were considered significant. The bars in the figure panels show the means and standard errors of the means (SEMs).
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    Differential IRGs and ISGs expressed during hMPV infection. A Heatmap of differentially expressed IRGs and ISGs with P values of < 0.05 in the hMPV group versus the control group and the RSV group. B Detailed expression levels of IRGs and ISGs with P values < 0.05 in the three groups. Statistical analysis was performed with an unpaired t -test. P values of 0.05 (∗), 0.01 (∗∗), and 0.001 (∗∗∗) were considered significant; NS: not significant. C Real-time PCR quantification of selected IRGs in infected and control cells at 24, 48, and 72 h postinfection. RSV and hMPV were propagated <t>in</t> <t>LLC-MK2</t> cells at a multiplicity of infection (MOI) of 0.1. N = 3. Statistical analysis was performed with an unpaired t -test. P values < 0.05 (∗), < 0.01 (∗∗), and < 0.0001 (∗∗∗∗) were considered significant. The bars in the figure panels show the means and standard errors of the means (SEMs).
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    Differential IRGs and ISGs expressed during hMPV infection. A Heatmap of differentially expressed IRGs and ISGs with P values of < 0.05 in the hMPV group versus the control group and the RSV group. B Detailed expression levels of IRGs and ISGs with P values < 0.05 in the three groups. Statistical analysis was performed with an unpaired t -test. P values of 0.05 (∗), 0.01 (∗∗), and 0.001 (∗∗∗) were considered significant; NS: not significant. C Real-time PCR quantification of selected IRGs in infected and control cells at 24, 48, and 72 h postinfection. RSV and hMPV were propagated in LLC-MK2 cells at a multiplicity of infection (MOI) of 0.1. N = 3. Statistical analysis was performed with an unpaired t -test. P values < 0.05 (∗), < 0.01 (∗∗), and < 0.0001 (∗∗∗∗) were considered significant. The bars in the figure panels show the means and standard errors of the means (SEMs).

    Journal: Virologica Sinica

    Article Title: Metatranscriptomics uncovers host immune and microbiome signatures specific to and shared between human metapneumovirus and respiratory syncytial virus infections in children

    doi: 10.1016/j.virs.2026.03.002

    Figure Lengend Snippet: Differential IRGs and ISGs expressed during hMPV infection. A Heatmap of differentially expressed IRGs and ISGs with P values of < 0.05 in the hMPV group versus the control group and the RSV group. B Detailed expression levels of IRGs and ISGs with P values < 0.05 in the three groups. Statistical analysis was performed with an unpaired t -test. P values of 0.05 (∗), 0.01 (∗∗), and 0.001 (∗∗∗) were considered significant; NS: not significant. C Real-time PCR quantification of selected IRGs in infected and control cells at 24, 48, and 72 h postinfection. RSV and hMPV were propagated in LLC-MK2 cells at a multiplicity of infection (MOI) of 0.1. N = 3. Statistical analysis was performed with an unpaired t -test. P values < 0.05 (∗), < 0.01 (∗∗), and < 0.0001 (∗∗∗∗) were considered significant. The bars in the figure panels show the means and standard errors of the means (SEMs).

    Article Snippet: Adult rhesus monkey kidney cells (LLC-MK2) (CCL-7) were obtained from ATCC (Manassas, VA, USA).

    Techniques: Infection, Control, Expressing, Real-time Polymerase Chain Reaction