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rhesus monkey kidney cell line llc mk2  (ATCC)


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    ATCC rhesus monkey kidney cell line llc mk2
    Rhesus Monkey Kidney Cell Line Llc Mk2, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 920 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/llc+mk2+rhesus+monkey+kidney+cells/LLC-MK2+Original/pm42215780-221-9-7
    Average 99 stars, based on 920 article reviews
    rhesus monkey kidney cell line llc mk2 - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Virus:

    Article Title: Chimeric human parainfluenza virus bearing the Ebola virus glycoprotein as the sole surface protein is immunogenic and highly protective against Ebola virus challenge
    Article Snippet: .. Cells, virus amplification and titration and plaque staining Stocks of HPIV3 and HPIV3/ΔF-HN/EboGP were prepared in LLC-MK2 Rhesus monkey kidney cells (American Type Culture Collection, Manassas, VA) with Opti-MEM medium (Invitrogen, Carlsbad, CA) containing 2.5% fetal bovine serum (Invitrogen). ..

    Amplification:

    Article Title: Chimeric human parainfluenza virus bearing the Ebola virus glycoprotein as the sole surface protein is immunogenic and highly protective against Ebola virus challenge
    Article Snippet: .. Cells, virus amplification and titration and plaque staining Stocks of HPIV3 and HPIV3/ΔF-HN/EboGP were prepared in LLC-MK2 Rhesus monkey kidney cells (American Type Culture Collection, Manassas, VA) with Opti-MEM medium (Invitrogen, Carlsbad, CA) containing 2.5% fetal bovine serum (Invitrogen). ..

    Titration:

    Article Title: Chimeric human parainfluenza virus bearing the Ebola virus glycoprotein as the sole surface protein is immunogenic and highly protective against Ebola virus challenge
    Article Snippet: .. Cells, virus amplification and titration and plaque staining Stocks of HPIV3 and HPIV3/ΔF-HN/EboGP were prepared in LLC-MK2 Rhesus monkey kidney cells (American Type Culture Collection, Manassas, VA) with Opti-MEM medium (Invitrogen, Carlsbad, CA) containing 2.5% fetal bovine serum (Invitrogen). ..

    Staining:

    Article Title: Chimeric human parainfluenza virus bearing the Ebola virus glycoprotein as the sole surface protein is immunogenic and highly protective against Ebola virus challenge
    Article Snippet: .. Cells, virus amplification and titration and plaque staining Stocks of HPIV3 and HPIV3/ΔF-HN/EboGP were prepared in LLC-MK2 Rhesus monkey kidney cells (American Type Culture Collection, Manassas, VA) with Opti-MEM medium (Invitrogen, Carlsbad, CA) containing 2.5% fetal bovine serum (Invitrogen). ..

    Cell Culture:

    Article Title: The Trypanosoma cruzi RNA-binding protein RBP42 is expressed in the cytoplasm throughout the life cycle of the parasite
    Article Snippet: Anti-tubulin antibody was from Abcam. .. LLC-MK2 rhesus monkey kidney cells were obtained from ATCC, and cultured in DMEM medium with 10% FBS. ..



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    rhesus monkey kidney cell line llc mk2  (ATCC)
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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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    Image Search Results


    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