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rhesus monkey kidney cell line llc mk2  (ATCC)


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    Structured Review

    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/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: Human norovirus persists longer than Escherichia coli in sandy soil, independent of plant decaying materials
    Article Snippet: A 1 mL of culture was centrifuged at 8,000 ×g for 3 min, resuspended in 1 mL of phosphate-buffered dilution water (PBDW, pH 7.2; Alpha Biosciences, Baltimore, MD, USA), reaching a final concentration of approximately 9 log 10 CFU/mL, and used for inoculation. .. Tulane virus was provided by L.A. Jaykus at North Carolina State University (Raleigh, NC) and propagated in rhesus monkey kidney cells (LLC-MK2, ATCC CCL-7TM) at a multiplicity of infection of 0.1. .. Infected cells were incubated at 37 °C with 5% CO 2 in Opti-MEMTM medium (Gibco Life Technologies, Grand Island, NY, USA) supplemented with 2% fetal bovine serum (FBS, GibcoTM, Thermo Fisher Scientific, USA), 1× antibiotic-antimycotic solution, 0.22% sodium bicarbonate, and 1× GlutaMAXTM (all from Gibco Life Technologies).

    Article Title: Human norovirus persists longer than Escherichia coli in sandy soil, independent of plant decaying materials.
    Article Snippet: A 1 mL of culture was centrifuged at 8,000 ×g for 3 min, resuspended in 1 mL of phosphate-buffered dilution water (PBDW, pH 7.2; Alpha Biosciences, Baltimore, MD, USA), reaching a final concentration of approximately 9 log10 CFU/mL, and used for inoculation. .. Tulane virus was provided by L.A. Jaykus at North Carolina State University (Raleigh, NC) and propagated in rhesus monkey kidney cells (LLC-MK2, ATCC CCL-7TM) at a multiplicity of infection of 0.1. .. Infected cells were incubated at 37°C with 5% CO2 in OptiMEMTM medium (Gibco Life Technologies, Grand Island, NY, USA) supplemented with 2% fetal bovine serum (FBS, GibcoTM, Thermo Fisher Scientific, USA), 1× antibioticantimycotic solution, 0.22% sodium bicarbonate, and 1× GlutaMAXTM (all from Gibco Life Technologies).

    Article Title: Persistence of human norovirus and Escherichia coli in preharvest agricultural water.
    Article Snippet: .. The virus stock was propagated by infecting a 90 % confluent monolayer of rhesus monkey kidney cells (LLC-MK2, ATCC CCL-7TM) at a 0.1 multiplicity of infection. .. Cells were cultured using complete growth medium composed of the base Opti-MEMTM medium (Gibco Life Technologies, Grand Island, NY, USA), supplemented with 2 % (v/v) fetal bovine serum (Gibco FBS, Thermo Fischer Scientific, Thornton, Australia), 1× antibiotic-antimycotic (Gibco Life Technologies), 0.22 % (v/w) sodium bicarbonate (Gibco), and 1× GlutaMAXTM (Gibco Life Technologies).

    Infection:

    Article Title: Human norovirus persists longer than Escherichia coli in sandy soil, independent of plant decaying materials
    Article Snippet: A 1 mL of culture was centrifuged at 8,000 ×g for 3 min, resuspended in 1 mL of phosphate-buffered dilution water (PBDW, pH 7.2; Alpha Biosciences, Baltimore, MD, USA), reaching a final concentration of approximately 9 log 10 CFU/mL, and used for inoculation. .. Tulane virus was provided by L.A. Jaykus at North Carolina State University (Raleigh, NC) and propagated in rhesus monkey kidney cells (LLC-MK2, ATCC CCL-7TM) at a multiplicity of infection of 0.1. .. Infected cells were incubated at 37 °C with 5% CO 2 in Opti-MEMTM medium (Gibco Life Technologies, Grand Island, NY, USA) supplemented with 2% fetal bovine serum (FBS, GibcoTM, Thermo Fisher Scientific, USA), 1× antibiotic-antimycotic solution, 0.22% sodium bicarbonate, and 1× GlutaMAXTM (all from Gibco Life Technologies).

    Article Title: Human norovirus persists longer than Escherichia coli in sandy soil, independent of plant decaying materials.
    Article Snippet: A 1 mL of culture was centrifuged at 8,000 ×g for 3 min, resuspended in 1 mL of phosphate-buffered dilution water (PBDW, pH 7.2; Alpha Biosciences, Baltimore, MD, USA), reaching a final concentration of approximately 9 log10 CFU/mL, and used for inoculation. .. Tulane virus was provided by L.A. Jaykus at North Carolina State University (Raleigh, NC) and propagated in rhesus monkey kidney cells (LLC-MK2, ATCC CCL-7TM) at a multiplicity of infection of 0.1. .. Infected cells were incubated at 37°C with 5% CO2 in OptiMEMTM medium (Gibco Life Technologies, Grand Island, NY, USA) supplemented with 2% fetal bovine serum (FBS, GibcoTM, Thermo Fisher Scientific, USA), 1× antibioticantimycotic solution, 0.22% sodium bicarbonate, and 1× GlutaMAXTM (all from Gibco Life Technologies).

    Article Title: Parechovirus-3 infection disrupts immunometabolism and leads to glutamate excitotoxicity in neural organoids.
    Article Snippet: .. In short, human colorectal adenocarcinoma (HT29) cells (HTB-38TM ATCC), rhesus monkey kidney cells (LLCMK2, provided by the Municipal Health Services, the Netherlands), African green monkey kidney cells (Vero, provided by the National Institute of Public Health and the 1 3 382 Page 8 of 12 Parechovirus-3 infection disrupts immunometabolism and leads to glutamate excitotoxicity in neural... at RT. ..

    Article Title: Persistence of human norovirus and Escherichia coli in preharvest agricultural water.
    Article Snippet: .. The virus stock was propagated by infecting a 90 % confluent monolayer of rhesus monkey kidney cells (LLC-MK2, ATCC CCL-7TM) at a 0.1 multiplicity of infection. .. Cells were cultured using complete growth medium composed of the base Opti-MEMTM medium (Gibco Life Technologies, Grand Island, NY, USA), supplemented with 2 % (v/v) fetal bovine serum (Gibco FBS, Thermo Fischer Scientific, Thornton, Australia), 1× antibiotic-antimycotic (Gibco Life Technologies), 0.22 % (v/w) sodium bicarbonate (Gibco), and 1× GlutaMAXTM (Gibco Life Technologies).

    Incubation:

    Article Title: Different Fc scaffolds enhance the breadth of in vitro neutralization of the same Fab against different Rotavirus strains
    Article Snippet: .. Rhesus monkey kidney cells (MA-104, ATCC) were propagated in complete medium (DMEM + 10% FBS + 1% Pen/Strep, Invitrogen) in a T75 flask and incubated at 37°C, 5% CO 2 and split 1:12 v:v every 2–3 days. .. Three different Rotavirus strains (Wa G1P[8], DS-1 G2P[4] and WI-61 G9P[8]) were purchased from American Type Culture Collection (ATCC) and propagated in MA-104 at low multiplicity of infection (MOI).



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    ATCC rhesus monkey kidney cell line llc mk2
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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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    ATCC rhesus monkey embryo kidney cell line ma104 cells
    Cytotoxicity and inhibitory effects on RV replication of different HSP90 inhibitors. ( A ) Plots for cell viability of <t>MA104,</t> Caco-2, and HT-29 cells after treatment with NVP-HSP990, GA, or 17-AAG at indicated concentrations for 24 h. Cell viability was tested using the CCK-8 assay. ( B ) Plots for RV (Wa and SA11 strains) inhibition in MA104, Caco-2, and HT-29 cells after treatment with NVP-HSP990, GA, or 17-AAG at indicated concentrations for 24 h. RV replication was tested by PFA, and IC 50 values are indicated at the top of each plot. The experiments were performed in triplicate, and the data are presented as mean ± SEM and are representative of four ( A ) and two ( B ) independent experiments. ns, not significant; * P < 0.05, ** P < 0.01, **** P < 0.0001 (two-way ANOVA).
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    ATCC fetal rhesus monkey kidney cells frhk 4
    Cytotoxicity and inhibitory effects on RV replication of different HSP90 inhibitors. ( A ) Plots for cell viability of <t>MA104,</t> Caco-2, and HT-29 cells after treatment with NVP-HSP990, GA, or 17-AAG at indicated concentrations for 24 h. Cell viability was tested using the CCK-8 assay. ( B ) Plots for RV (Wa and SA11 strains) inhibition in MA104, Caco-2, and HT-29 cells after treatment with NVP-HSP990, GA, or 17-AAG at indicated concentrations for 24 h. RV replication was tested by PFA, and IC 50 values are indicated at the top of each plot. The experiments were performed in triplicate, and the data are presented as mean ± SEM and are representative of four ( A ) and two ( B ) independent experiments. ns, not significant; * P < 0.05, ** P < 0.01, **** P < 0.0001 (two-way ANOVA).
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    ATCC rhesus monkey kidney epithelial cell llm mk2
    Cytotoxicity and inhibitory effects on RV replication of different HSP90 inhibitors. ( A ) Plots for cell viability of <t>MA104,</t> Caco-2, and HT-29 cells after treatment with NVP-HSP990, GA, or 17-AAG at indicated concentrations for 24 h. Cell viability was tested using the CCK-8 assay. ( B ) Plots for RV (Wa and SA11 strains) inhibition in MA104, Caco-2, and HT-29 cells after treatment with NVP-HSP990, GA, or 17-AAG at indicated concentrations for 24 h. RV replication was tested by PFA, and IC 50 values are indicated at the top of each plot. The experiments were performed in triplicate, and the data are presented as mean ± SEM and are representative of four ( A ) and two ( B ) independent experiments. ns, not significant; * P < 0.05, ** P < 0.01, **** P < 0.0001 (two-way ANOVA).
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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

    Cytotoxicity and inhibitory effects on RV replication of different HSP90 inhibitors. ( A ) Plots for cell viability of MA104, Caco-2, and HT-29 cells after treatment with NVP-HSP990, GA, or 17-AAG at indicated concentrations for 24 h. Cell viability was tested using the CCK-8 assay. ( B ) Plots for RV (Wa and SA11 strains) inhibition in MA104, Caco-2, and HT-29 cells after treatment with NVP-HSP990, GA, or 17-AAG at indicated concentrations for 24 h. RV replication was tested by PFA, and IC 50 values are indicated at the top of each plot. The experiments were performed in triplicate, and the data are presented as mean ± SEM and are representative of four ( A ) and two ( B ) independent experiments. ns, not significant; * P < 0.05, ** P < 0.01, **** P < 0.0001 (two-way ANOVA).

    Journal: Journal of Virology

    Article Title: A small-molecule HSP90 inhibitor, NVP-HSP990, alleviates rotavirus infection

    doi: 10.1128/jvi.01883-25

    Figure Lengend Snippet: Cytotoxicity and inhibitory effects on RV replication of different HSP90 inhibitors. ( A ) Plots for cell viability of MA104, Caco-2, and HT-29 cells after treatment with NVP-HSP990, GA, or 17-AAG at indicated concentrations for 24 h. Cell viability was tested using the CCK-8 assay. ( B ) Plots for RV (Wa and SA11 strains) inhibition in MA104, Caco-2, and HT-29 cells after treatment with NVP-HSP990, GA, or 17-AAG at indicated concentrations for 24 h. RV replication was tested by PFA, and IC 50 values are indicated at the top of each plot. The experiments were performed in triplicate, and the data are presented as mean ± SEM and are representative of four ( A ) and two ( B ) independent experiments. ns, not significant; * P < 0.05, ** P < 0.01, **** P < 0.0001 (two-way ANOVA).

    Article Snippet: Rhesus monkey embryo kidney cell line MA104 cells (ATCC: CRL-2378.1) were provided by Dr. Elschner (Friedrich-Loeffler-Institute).

    Techniques: CCK-8 Assay, Inhibition

    NVP-HSP990 inhibited MAPK activation and facilitated expression of tight junction-associated proteins in intestinal cells. ( A ) MA104, Caco-2, and HT-29 cells were mock-infected with PBS or infected with RV Wa or SA11 strains (MOI = 3), followed by treatment of 100 nM HSP990 (+) or an equal volume of DMSO as a control (−) for 20 h. Then the infected cells were harvested for WB analysis of MAPK components. ( B ) Caco-2 cells were mock-infected with PBS, treated with 1 µM C16-PAF(C16), or infected with RV Wa or SA11 strains (MOI = 3), and then treated with 100 nM HSP990 (+) or DMSO as a control (−) for 20 h. The infected cells were harvested for WB analysis of MAPK components. ( C ) Caco-2 cells were mock-infected with PBS or infected with RV Wa or SA11 strains (MOI = 3), and then treated with 100 nM HSP990 (+) or DMSO as control (−) for 20 h. Then the infected cells were harvested for WB analysis of tight junction-associated proteins. Data are representative of three ( A ) and two ( B and C ) independent experiments.

    Journal: Journal of Virology

    Article Title: A small-molecule HSP90 inhibitor, NVP-HSP990, alleviates rotavirus infection

    doi: 10.1128/jvi.01883-25

    Figure Lengend Snippet: NVP-HSP990 inhibited MAPK activation and facilitated expression of tight junction-associated proteins in intestinal cells. ( A ) MA104, Caco-2, and HT-29 cells were mock-infected with PBS or infected with RV Wa or SA11 strains (MOI = 3), followed by treatment of 100 nM HSP990 (+) or an equal volume of DMSO as a control (−) for 20 h. Then the infected cells were harvested for WB analysis of MAPK components. ( B ) Caco-2 cells were mock-infected with PBS, treated with 1 µM C16-PAF(C16), or infected with RV Wa or SA11 strains (MOI = 3), and then treated with 100 nM HSP990 (+) or DMSO as a control (−) for 20 h. The infected cells were harvested for WB analysis of MAPK components. ( C ) Caco-2 cells were mock-infected with PBS or infected with RV Wa or SA11 strains (MOI = 3), and then treated with 100 nM HSP990 (+) or DMSO as control (−) for 20 h. Then the infected cells were harvested for WB analysis of tight junction-associated proteins. Data are representative of three ( A ) and two ( B and C ) independent experiments.

    Article Snippet: Rhesus monkey embryo kidney cell line MA104 cells (ATCC: CRL-2378.1) were provided by Dr. Elschner (Friedrich-Loeffler-Institute).

    Techniques: Activation Assay, Expressing, Infection, Control