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upci scc090 cells  (DSMZ)


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    Structured Review

    DSMZ upci scc090 cells
    Upci Scc090 Cells, supplied by DSMZ, used in various techniques. Bioz Stars score: 92/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/upci+scc090+cells/UPCI-SCC-090/pm38137525-52-2-15
    Average 92 stars, based on 7 article reviews
    upci scc090 cells - by Bioz Stars, 2026-11
    92/100 stars

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    Related Articles

    Cell Culture:

    Article Title: Brain-Derived Neurotrophin and TrkB in Head and Neck Squamous Cell Carcinoma
    Article Snippet: Dot Plots, frequency diagrams, and heat maps were created using TissueQuest (TissueGnostics ® ) [ , ]. .. The SCC-25 and UPCI-SCC090 cells were acquired from the German Collection of Microorganisms and Cell Cultures (DSMZ, Braunschweig, Germany, DSMZ no.: ACC 617), SCC-25 cells were cultured in DMEM/F12 medium [ , ], UPCI-SCC090 [ ] cells in EMEM medium supplemented with 10% FBS, 2 mM l-glutamine, 100 units/mL penicillin, and 100 μg/mL streptomycin [ ]. .. Detroit 562 cells were purchased from Cell Lines Service (CLS, Eppelheim, Germany) and were cultured in EMEM medium [ ] supplemented with 10% FBS, 2 mM l-glutamine, 100 units/mL penicillin, and 100 μg/mL streptomycin.



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    The effect of irradiation (IR) on cell survival and tumor growth. (A) Survival of cells after in vitro IR with 2, 4, 6, 8, and 10 Gy (n = 3). (B) Kaplan-Meier survival curve for mice bearing pharyngeal squamous cell carcinoma <t>(PSCC)</t> tumors treated with either a single dose of 8 Gy or 3×8 Gy, complete response (CR) (n = 6). Data are presented as mean ± standard error of the mean (SEM); # = indicates p < 0.05 for comparisons <t>between</t> <t>UPCI:SCC090</t> and other cell lines or tumor models; * = indicates p < 0.05 for comparisons between IR doses within the same cell line or tumor model.
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    The effect of irradiation (IR) on cell survival and tumor growth. (A) Survival of cells after in vitro IR with 2, 4, 6, 8, and 10 Gy (n = 3). (B) Kaplan-Meier survival curve for mice bearing pharyngeal squamous cell carcinoma <t>(PSCC)</t> tumors treated with either a single dose of 8 Gy or 3×8 Gy, complete response (CR) (n = 6). Data are presented as mean ± standard error of the mean (SEM); # = indicates p < 0.05 for comparisons <t>between</t> <t>UPCI:SCC090</t> and other cell lines or tumor models; * = indicates p < 0.05 for comparisons between IR doses within the same cell line or tumor model.
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    The effect of irradiation (IR) on cell survival and tumor growth. (A) Survival of cells after in vitro IR with 2, 4, 6, 8, and 10 Gy (n = 3). (B) Kaplan-Meier survival curve for mice bearing pharyngeal squamous cell carcinoma <t>(PSCC)</t> tumors treated with either a single dose of 8 Gy or 3×8 Gy, complete response (CR) (n = 6). Data are presented as mean ± standard error of the mean (SEM); # = indicates p < 0.05 for comparisons <t>between</t> <t>UPCI:SCC090</t> and other cell lines or tumor models; * = indicates p < 0.05 for comparisons between IR doses within the same cell line or tumor model.
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    scc90  (ATCC)
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    ATCC scc90
    HNSSC cell lines SCC47, FaDu, RPMI2650, SCC4, and <t>SCC90</t> were imaged for Ca2+ responses with bitter agonists. (A and B) SCC47 Ca2+ response over time (A) and peak Ca2+ responses (B) with lidocaine; mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS with each concentration of lidocaine. (C and D) SCC47 Ca2+ response over time (C) and peak Ca2+ responses (D) with denatonium benzoate; mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS to each concentration of denatonium. (E) Ca2+ dose response of lidocaine in SCC47 cells. (F–H) SCC47 (F), FaDu (G), and RPMI2650 (H) peak Ca2+ responses with HBSS, lidocaine, denatonium benzoate, thujone, flufenamic acid (FFA), or ATP. Mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS to each agonist. (I–K) SCC4 (I), SCC90 (J), and FaDu (K) peak fluorescent Ca2+ responses with lidocaine; mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS to each concentration of lidocaine. (L) SCC47 peak Ca2+ response with lidocaine or procaine; mean ± SEM with >3 experiments using separate cultures. Significance by unpaired t test. *p < 0.05, **p < 0.01, ***p < 0.001; ns, no statistical significance.
    Scc90, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    DSMZ upci scc090 cells
    HNSSC cell lines SCC47, FaDu, RPMI2650, SCC4, and <t>SCC90</t> were imaged for Ca2+ responses with bitter agonists. (A and B) SCC47 Ca2+ response over time (A) and peak Ca2+ responses (B) with lidocaine; mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS with each concentration of lidocaine. (C and D) SCC47 Ca2+ response over time (C) and peak Ca2+ responses (D) with denatonium benzoate; mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS to each concentration of denatonium. (E) Ca2+ dose response of lidocaine in SCC47 cells. (F–H) SCC47 (F), FaDu (G), and RPMI2650 (H) peak Ca2+ responses with HBSS, lidocaine, denatonium benzoate, thujone, flufenamic acid (FFA), or ATP. Mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS to each agonist. (I–K) SCC4 (I), SCC90 (J), and FaDu (K) peak fluorescent Ca2+ responses with lidocaine; mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS to each concentration of lidocaine. (L) SCC47 peak Ca2+ response with lidocaine or procaine; mean ± SEM with >3 experiments using separate cultures. Significance by unpaired t test. *p < 0.05, **p < 0.01, ***p < 0.001; ns, no statistical significance.
    Upci Scc090 Cells, supplied by DSMZ, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 92 stars, based on 1 article reviews
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    ATCC upci scc090
    HNSSC cell lines SCC47, FaDu, RPMI2650, SCC4, and <t>SCC90</t> were imaged for Ca2+ responses with bitter agonists. (A and B) SCC47 Ca2+ response over time (A) and peak Ca2+ responses (B) with lidocaine; mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS with each concentration of lidocaine. (C and D) SCC47 Ca2+ response over time (C) and peak Ca2+ responses (D) with denatonium benzoate; mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS to each concentration of denatonium. (E) Ca2+ dose response of lidocaine in SCC47 cells. (F–H) SCC47 (F), FaDu (G), and RPMI2650 (H) peak Ca2+ responses with HBSS, lidocaine, denatonium benzoate, thujone, flufenamic acid (FFA), or ATP. Mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS to each agonist. (I–K) SCC4 (I), SCC90 (J), and FaDu (K) peak fluorescent Ca2+ responses with lidocaine; mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS to each concentration of lidocaine. (L) SCC47 peak Ca2+ response with lidocaine or procaine; mean ± SEM with >3 experiments using separate cultures. Significance by unpaired t test. *p < 0.05, **p < 0.01, ***p < 0.001; ns, no statistical significance.
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    ATCC epi thelial cells oscc
    HNSSC cell lines SCC47, FaDu, RPMI2650, SCC4, and <t>SCC90</t> were imaged for Ca2+ responses with bitter agonists. (A and B) SCC47 Ca2+ response over time (A) and peak Ca2+ responses (B) with lidocaine; mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS with each concentration of lidocaine. (C and D) SCC47 Ca2+ response over time (C) and peak Ca2+ responses (D) with denatonium benzoate; mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS to each concentration of denatonium. (E) Ca2+ dose response of lidocaine in SCC47 cells. (F–H) SCC47 (F), FaDu (G), and RPMI2650 (H) peak Ca2+ responses with HBSS, lidocaine, denatonium benzoate, thujone, flufenamic acid (FFA), or ATP. Mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS to each agonist. (I–K) SCC4 (I), SCC90 (J), and FaDu (K) peak fluorescent Ca2+ responses with lidocaine; mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS to each concentration of lidocaine. (L) SCC47 peak Ca2+ response with lidocaine or procaine; mean ± SEM with >3 experiments using separate cultures. Significance by unpaired t test. *p < 0.05, **p < 0.01, ***p < 0.001; ns, no statistical significance.
    Epi Thelial Cells Oscc, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC oral squamous cell carcinoma
    HNSSC cell lines SCC47, FaDu, RPMI2650, SCC4, and <t>SCC90</t> were imaged for Ca2+ responses with bitter agonists. (A and B) SCC47 Ca2+ response over time (A) and peak Ca2+ responses (B) with lidocaine; mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS with each concentration of lidocaine. (C and D) SCC47 Ca2+ response over time (C) and peak Ca2+ responses (D) with denatonium benzoate; mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS to each concentration of denatonium. (E) Ca2+ dose response of lidocaine in SCC47 cells. (F–H) SCC47 (F), FaDu (G), and RPMI2650 (H) peak Ca2+ responses with HBSS, lidocaine, denatonium benzoate, thujone, flufenamic acid (FFA), or ATP. Mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS to each agonist. (I–K) SCC4 (I), SCC90 (J), and FaDu (K) peak fluorescent Ca2+ responses with lidocaine; mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS to each concentration of lidocaine. (L) SCC47 peak Ca2+ response with lidocaine or procaine; mean ± SEM with >3 experiments using separate cultures. Significance by unpaired t test. *p < 0.05, **p < 0.01, ***p < 0.001; ns, no statistical significance.
    Oral Squamous Cell Carcinoma, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    The effect of irradiation (IR) on cell survival and tumor growth. (A) Survival of cells after in vitro IR with 2, 4, 6, 8, and 10 Gy (n = 3). (B) Kaplan-Meier survival curve for mice bearing pharyngeal squamous cell carcinoma (PSCC) tumors treated with either a single dose of 8 Gy or 3×8 Gy, complete response (CR) (n = 6). Data are presented as mean ± standard error of the mean (SEM); # = indicates p < 0.05 for comparisons between UPCI:SCC090 and other cell lines or tumor models; * = indicates p < 0.05 for comparisons between IR doses within the same cell line or tumor model.

    Journal: Radiology and Oncology

    Article Title: Human papillomavirus-related oropharyngeal squamous cell carcinoma exhibits enhanced radiosensitivity despite limited activation of cytosolic DNA sensing pathways and innate immune responses

    doi: 10.2478/raon-2025-0057

    Figure Lengend Snippet: The effect of irradiation (IR) on cell survival and tumor growth. (A) Survival of cells after in vitro IR with 2, 4, 6, 8, and 10 Gy (n = 3). (B) Kaplan-Meier survival curve for mice bearing pharyngeal squamous cell carcinoma (PSCC) tumors treated with either a single dose of 8 Gy or 3×8 Gy, complete response (CR) (n = 6). Data are presented as mean ± standard error of the mean (SEM); # = indicates p < 0.05 for comparisons between UPCI:SCC090 and other cell lines or tumor models; * = indicates p < 0.05 for comparisons between IR doses within the same cell line or tumor model.

    Article Snippet: The in vitro experiments were performed with four human PSCC cell lines: HPV16-related OPSCC UPCI:SCC090 (RRID:CVCL_1899; ATCC ® CRL-3239TM, Manassas, VA, USA), HPV16-unrelated OPSCC UM-SCC-6 (RRID:CVCL_7773; Merck-Millipore, Burlington, MA, USA), HPV16-related hypopharyngeal squamous cell carcinoma (HPSCC) 2A3 (RRID:CVCL_0D71; ATCC ® CRL-3212TM, ATCC), and HPV16-unrelated HPSCC FaDu (RRID:CVCL_1218; ATCC ® HTB-43TM, ATCC).

    Techniques: Irradiation, In Vitro

    Irradiation (IR)-induced accumulation of dsDNA in the cytosol of pharyngeal squamous cell carcinoma (PSCC) cells. (A) Accumulation of dsDNA in the cytosol of cells 72 hours after IR. Green: dsDNA (anti-dsDNA), red: plasma membrane (WGA), blue: nucleus (Hoechst 33342), Scale bar = 10 μm. (B) Number of dsDNA spots per cell in cytosol 72 hours after IR with 4, 8, or 3x8 Gy (n = 8). Data is represented as mean ± standard error of the mean (SEM). # = indicates p < 0.05 for comparisons between UPCI:SCC090 and other cell lines or tumor models; * = indicates p < 0.05 for comparisons between IR doses within the same cell line or tumor model; o = indicates p < 0.05 for comparisons between FaDu and 2A3 models; + = indicates p < 0.05 for comparisons between UM-SCC-6 and FaDu

    Journal: Radiology and Oncology

    Article Title: Human papillomavirus-related oropharyngeal squamous cell carcinoma exhibits enhanced radiosensitivity despite limited activation of cytosolic DNA sensing pathways and innate immune responses

    doi: 10.2478/raon-2025-0057

    Figure Lengend Snippet: Irradiation (IR)-induced accumulation of dsDNA in the cytosol of pharyngeal squamous cell carcinoma (PSCC) cells. (A) Accumulation of dsDNA in the cytosol of cells 72 hours after IR. Green: dsDNA (anti-dsDNA), red: plasma membrane (WGA), blue: nucleus (Hoechst 33342), Scale bar = 10 μm. (B) Number of dsDNA spots per cell in cytosol 72 hours after IR with 4, 8, or 3x8 Gy (n = 8). Data is represented as mean ± standard error of the mean (SEM). # = indicates p < 0.05 for comparisons between UPCI:SCC090 and other cell lines or tumor models; * = indicates p < 0.05 for comparisons between IR doses within the same cell line or tumor model; o = indicates p < 0.05 for comparisons between FaDu and 2A3 models; + = indicates p < 0.05 for comparisons between UM-SCC-6 and FaDu

    Article Snippet: The in vitro experiments were performed with four human PSCC cell lines: HPV16-related OPSCC UPCI:SCC090 (RRID:CVCL_1899; ATCC ® CRL-3239TM, Manassas, VA, USA), HPV16-unrelated OPSCC UM-SCC-6 (RRID:CVCL_7773; Merck-Millipore, Burlington, MA, USA), HPV16-related hypopharyngeal squamous cell carcinoma (HPSCC) 2A3 (RRID:CVCL_0D71; ATCC ® CRL-3212TM, ATCC), and HPV16-unrelated HPSCC FaDu (RRID:CVCL_1218; ATCC ® HTB-43TM, ATCC).

    Techniques: Irradiation, Clinical Proteomics, Membrane

    Effect of irradiation (IR) on cytokine gene expression in tumor cells and tumor microenvironment (TME) of pharyngeal squamous cell carcinoma (PSCC). (A–C) Fold change in expression of IFNβ (A) , tumor necrosis factor (TNF)α (B) , and IL1β (C) in vitro 72 hours after IR with 4, 8, or 3x8 Gy, normalized to housekeeping genes (GUSB and B2M) and respective controls (n = 3). (D–F) Fold change in expression of IFNβ (D) , TNFa (E) , and IL1 β (F) in tumor cells in vivo 72 hours after IR with 8 or 3×8 Gy, normalized to housekeeping genes (GUSB and B2M) and control (n = 5). (G–I) Fold change in expression of Ifnβ (G) , TNFα (H) , and Il1β (I) in the TME in vivo 72 hours after IR with 8 or 3–8 Gy, normalized to housekeeping genes (BA and GADPH) and control (n = 5). Data is represented as mean ± standard error of the mean (SEM). # = indicates p < 0.05 for comparisons between UPCI:SCC090 and other cell lines or tumor models; * = indicates p < 0.05 for comparisons between IR doses within the same cell line or tumor model; o = indicates p < 0.05 for comparisons between FaDu and 2A3 models; + = indicates p < 0.05 for comparisons between UM-SCC-6 and FaDu

    Journal: Radiology and Oncology

    Article Title: Human papillomavirus-related oropharyngeal squamous cell carcinoma exhibits enhanced radiosensitivity despite limited activation of cytosolic DNA sensing pathways and innate immune responses

    doi: 10.2478/raon-2025-0057

    Figure Lengend Snippet: Effect of irradiation (IR) on cytokine gene expression in tumor cells and tumor microenvironment (TME) of pharyngeal squamous cell carcinoma (PSCC). (A–C) Fold change in expression of IFNβ (A) , tumor necrosis factor (TNF)α (B) , and IL1β (C) in vitro 72 hours after IR with 4, 8, or 3x8 Gy, normalized to housekeeping genes (GUSB and B2M) and respective controls (n = 3). (D–F) Fold change in expression of IFNβ (D) , TNFa (E) , and IL1 β (F) in tumor cells in vivo 72 hours after IR with 8 or 3×8 Gy, normalized to housekeeping genes (GUSB and B2M) and control (n = 5). (G–I) Fold change in expression of Ifnβ (G) , TNFα (H) , and Il1β (I) in the TME in vivo 72 hours after IR with 8 or 3–8 Gy, normalized to housekeeping genes (BA and GADPH) and control (n = 5). Data is represented as mean ± standard error of the mean (SEM). # = indicates p < 0.05 for comparisons between UPCI:SCC090 and other cell lines or tumor models; * = indicates p < 0.05 for comparisons between IR doses within the same cell line or tumor model; o = indicates p < 0.05 for comparisons between FaDu and 2A3 models; + = indicates p < 0.05 for comparisons between UM-SCC-6 and FaDu

    Article Snippet: The in vitro experiments were performed with four human PSCC cell lines: HPV16-related OPSCC UPCI:SCC090 (RRID:CVCL_1899; ATCC ® CRL-3239TM, Manassas, VA, USA), HPV16-unrelated OPSCC UM-SCC-6 (RRID:CVCL_7773; Merck-Millipore, Burlington, MA, USA), HPV16-related hypopharyngeal squamous cell carcinoma (HPSCC) 2A3 (RRID:CVCL_0D71; ATCC ® CRL-3212TM, ATCC), and HPV16-unrelated HPSCC FaDu (RRID:CVCL_1218; ATCC ® HTB-43TM, ATCC).

    Techniques: Irradiation, Gene Expression, Expressing, In Vitro, In Vivo, Control

    HNSSC cell lines SCC47, FaDu, RPMI2650, SCC4, and SCC90 were imaged for Ca2+ responses with bitter agonists. (A and B) SCC47 Ca2+ response over time (A) and peak Ca2+ responses (B) with lidocaine; mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS with each concentration of lidocaine. (C and D) SCC47 Ca2+ response over time (C) and peak Ca2+ responses (D) with denatonium benzoate; mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS to each concentration of denatonium. (E) Ca2+ dose response of lidocaine in SCC47 cells. (F–H) SCC47 (F), FaDu (G), and RPMI2650 (H) peak Ca2+ responses with HBSS, lidocaine, denatonium benzoate, thujone, flufenamic acid (FFA), or ATP. Mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS to each agonist. (I–K) SCC4 (I), SCC90 (J), and FaDu (K) peak fluorescent Ca2+ responses with lidocaine; mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS to each concentration of lidocaine. (L) SCC47 peak Ca2+ response with lidocaine or procaine; mean ± SEM with >3 experiments using separate cultures. Significance by unpaired t test. *p < 0.05, **p < 0.01, ***p < 0.001; ns, no statistical significance.

    Journal: Cell reports

    Article Title: Lidocaine induces apoptosis in head and neck squamous cell carcinoma through activation of bitter taste receptor T2R14

    doi: 10.1016/j.celrep.2023.113437

    Figure Lengend Snippet: HNSSC cell lines SCC47, FaDu, RPMI2650, SCC4, and SCC90 were imaged for Ca2+ responses with bitter agonists. (A and B) SCC47 Ca2+ response over time (A) and peak Ca2+ responses (B) with lidocaine; mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS with each concentration of lidocaine. (C and D) SCC47 Ca2+ response over time (C) and peak Ca2+ responses (D) with denatonium benzoate; mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS to each concentration of denatonium. (E) Ca2+ dose response of lidocaine in SCC47 cells. (F–H) SCC47 (F), FaDu (G), and RPMI2650 (H) peak Ca2+ responses with HBSS, lidocaine, denatonium benzoate, thujone, flufenamic acid (FFA), or ATP. Mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS to each agonist. (I–K) SCC4 (I), SCC90 (J), and FaDu (K) peak fluorescent Ca2+ responses with lidocaine; mean ± SEM with >3 experiments using separate cultures. Significance by one-way ANOVA with Bonferroni post-test comparing HBSS to each concentration of lidocaine. (L) SCC47 peak Ca2+ response with lidocaine or procaine; mean ± SEM with >3 experiments using separate cultures. Significance by unpaired t test. *p < 0.05, **p < 0.01, ***p < 0.001; ns, no statistical significance.

    Article Snippet: SCC90 , ATCC , CRL-3239.

    Techniques: Concentration Assay

    KEY RESOURCES TABLE

    Journal: Cell reports

    Article Title: Lidocaine induces apoptosis in head and neck squamous cell carcinoma through activation of bitter taste receptor T2R14

    doi: 10.1016/j.celrep.2023.113437

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: SCC90 , ATCC , CRL-3239.

    Techniques: Virus, Recombinant, Reverse Transcription, DC Protein Assay, Western Blot, CRISPR, Control, Expressing, TaqMan Assay, shRNA, Software