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  • 99
    Thermo Fisher tnf α
    Inhibitory effects of SCRT on LPS-induced production of the pro-inflammatory cytokines (A) <t>TNF-α,</t> (B) IL-1β and (C) IL-6 in RAW 264.7 cells. The cells (5×10 5 /ml) were treated with SCRT (0.25, 0.5 and 1 mg/ml) for 1 h, followed by induction with 1 μ g/ml LPS for 20 h. Control cells were incubated with vehicle alone. The levels of the pro-inflammatory cytokines were measured using ELISA. Values are expressed as the mean ± standard deviation of 3 replicates for each condition. ** P
    Tnf α, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/tnf α/product/Thermo Fisher
    Average 99 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    tnf α - by Bioz Stars, 2021-06
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    86
    R&D Systems tnf α
    Effects of <t>TNF-α</t> and rapamycin on expression of TNF-α, IL-8, and IL-6
    Tnf α, supplied by R&D Systems, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/tnf α/product/R&D Systems
    Average 86 stars, based on 1 article reviews
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    96
    Millipore tnf α
    The construction of human ALIM infected by Streptococcus . A. The relative LDH vitality of supernates in ALIM at 4 h, 24 h and 48 h. B. The relative expression of IL-6, IL-8 and <t>TNF-α</t> of supernates in ALIM. LDH, lactate
    Tnf α, supplied by Millipore, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/tnf α/product/Millipore
    Average 96 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
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    99
    PeproTech tnf α
    <t>TNF-α</t> induces Bcl6 gene expression in the hepatocytes and Bcl6 overexpression upregulates the TNF-α levels in vivo . (A) The RNA levels of Tnf- α, Il-6, Il-12, Cxcl9, and Cxcl10 were examined by RT-qPCR in B6.2- and B6.2S-injected mouse liver isolated during the HBV clearance stage. (B) AML12 cells were treated with or without TNF-α (100 ng/ml) for the indicated time periods and Bcl6 RNA was analyzed by RT-qPCR. The induction fold means the ratio of the Bcl6 RNA levels in the presence of TNF-α over those without TNF-α. (C) AML12 and Huh-7 cells were transfected with 1 μg of vector or the Bcl6 -expressing plasmid. Two days later, the TNF-α RNA levels were analyzed by RT-qPCR analysis. (D) The liver RNA from the B6.2 or the (B6.2 + Bcl6 ) mice at 2 w.p.i. were analyzed for Tnf- α expression by RT-qPCR. In (A–D) , * P
    Tnf α, supplied by PeproTech, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/tnf α/product/PeproTech
    Average 99 stars, based on 1 article reviews
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    N/A
    Tumor necrosis factor α TNF α is produced by cells that are involved in inflammatory immune responses TNF α is secreted by activated CD4 T cells monocytes macrophages NK cells
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    N/A
    The peptide PSTHVLITHTI corresponds to residues 70 80 of human TNF α substituted with Ile at position 76 and exhibits many of the biological activities found for TNF α Ile⁷⁶
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    N/A
    TNF α antagonist is an exocyclic peptide that mimics the critical TNF α recognition loop on TNF receptor I complex and thus prevents ligand interaction with the receptor By blocking
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    Image Search Results


    Inhibitory effects of SCRT on LPS-induced production of the pro-inflammatory cytokines (A) TNF-α, (B) IL-1β and (C) IL-6 in RAW 264.7 cells. The cells (5×10 5 /ml) were treated with SCRT (0.25, 0.5 and 1 mg/ml) for 1 h, followed by induction with 1 μ g/ml LPS for 20 h. Control cells were incubated with vehicle alone. The levels of the pro-inflammatory cytokines were measured using ELISA. Values are expressed as the mean ± standard deviation of 3 replicates for each condition. ** P

    Journal: International Journal of Molecular Medicine

    Article Title: Amelioration of inflammatory responses by Socheongryong-Tang, a traditional herbal medicine, in RAW 264.7 cells and rats

    doi: 10.3892/ijmm.2018.3465

    Figure Lengend Snippet: Inhibitory effects of SCRT on LPS-induced production of the pro-inflammatory cytokines (A) TNF-α, (B) IL-1β and (C) IL-6 in RAW 264.7 cells. The cells (5×10 5 /ml) were treated with SCRT (0.25, 0.5 and 1 mg/ml) for 1 h, followed by induction with 1 μ g/ml LPS for 20 h. Control cells were incubated with vehicle alone. The levels of the pro-inflammatory cytokines were measured using ELISA. Values are expressed as the mean ± standard deviation of 3 replicates for each condition. ** P

    Article Snippet: The immunoassay kit (cat. no. KGE004B) for PGE2 was obtained from R & D Systems (Minneapolis, MN, USA) and ELISA kits for IL-1β (cat. no. EMIL1B), IL-6 (cat. no. EM2IL6) and TNF-α (cat. no. EMTNFA) were purchased from Pierce (Thermo Fisher Scientific, Inc., Waltham, MA, USA).

    Techniques: Incubation, Enzyme-linked Immunosorbent Assay, Standard Deviation

    Effects of TNF-α and rapamycin on expression of TNF-α, IL-8, and IL-6

    Journal:

    Article Title: Reactive Oxygen Species in Tumor Necrosis Factor-?-Activated Primary Human Keratinocytes: Implications for Psoriasis and Inflammatory Skin Disease

    doi: 10.1038/jid.2008.122

    Figure Lengend Snippet: Effects of TNF-α and rapamycin on expression of TNF-α, IL-8, and IL-6

    Article Snippet: TNF-α was obtained from R & D Systems (Minneapolis, MN).

    Techniques: Expressing

    Effect of hydrogen peroxide on TNF-α-induced gene expression in primary human keratinocytes

    Journal:

    Article Title: Reactive Oxygen Species in Tumor Necrosis Factor-?-Activated Primary Human Keratinocytes: Implications for Psoriasis and Inflammatory Skin Disease

    doi: 10.1038/jid.2008.122

    Figure Lengend Snippet: Effect of hydrogen peroxide on TNF-α-induced gene expression in primary human keratinocytes

    Article Snippet: TNF-α was obtained from R & D Systems (Minneapolis, MN).

    Techniques: Expressing

    Effects of rapamycin and antioxidants on hydrogen peroxide production induced by TNF-α in primary human keratinocytes

    Journal:

    Article Title: Reactive Oxygen Species in Tumor Necrosis Factor-?-Activated Primary Human Keratinocytes: Implications for Psoriasis and Inflammatory Skin Disease

    doi: 10.1038/jid.2008.122

    Figure Lengend Snippet: Effects of rapamycin and antioxidants on hydrogen peroxide production induced by TNF-α in primary human keratinocytes

    Article Snippet: TNF-α was obtained from R & D Systems (Minneapolis, MN).

    Techniques:

    Effects of antioxidants on TNF-α-induced IκB degradation in primary human keratinocytes

    Journal:

    Article Title: Reactive Oxygen Species in Tumor Necrosis Factor-?-Activated Primary Human Keratinocytes: Implications for Psoriasis and Inflammatory Skin Disease

    doi: 10.1038/jid.2008.122

    Figure Lengend Snippet: Effects of antioxidants on TNF-α-induced IκB degradation in primary human keratinocytes

    Article Snippet: TNF-α was obtained from R & D Systems (Minneapolis, MN).

    Techniques:

    Dose response of hydrogen peroxide production induced by TNF-α in primary human keratinocytes

    Journal:

    Article Title: Reactive Oxygen Species in Tumor Necrosis Factor-?-Activated Primary Human Keratinocytes: Implications for Psoriasis and Inflammatory Skin Disease

    doi: 10.1038/jid.2008.122

    Figure Lengend Snippet: Dose response of hydrogen peroxide production induced by TNF-α in primary human keratinocytes

    Article Snippet: TNF-α was obtained from R & D Systems (Minneapolis, MN).

    Techniques:

    Degradation of IκB(α) induced by TNF-α in primary human keratinocytes

    Journal:

    Article Title: Reactive Oxygen Species in Tumor Necrosis Factor-?-Activated Primary Human Keratinocytes: Implications for Psoriasis and Inflammatory Skin Disease

    doi: 10.1038/jid.2008.122

    Figure Lengend Snippet: Degradation of IκB(α) induced by TNF-α in primary human keratinocytes

    Article Snippet: TNF-α was obtained from R & D Systems (Minneapolis, MN).

    Techniques:

    Nuclear translocation of the NF-κB p65 subunit induced by TNF-α in primary human keratinocytes

    Journal:

    Article Title: Reactive Oxygen Species in Tumor Necrosis Factor-?-Activated Primary Human Keratinocytes: Implications for Psoriasis and Inflammatory Skin Disease

    doi: 10.1038/jid.2008.122

    Figure Lengend Snippet: Nuclear translocation of the NF-κB p65 subunit induced by TNF-α in primary human keratinocytes

    Article Snippet: TNF-α was obtained from R & D Systems (Minneapolis, MN).

    Techniques: Translocation Assay

    Effects of rapamycin on TNF-α-induced IκB degradation in primary human keratinocytes

    Journal:

    Article Title: Reactive Oxygen Species in Tumor Necrosis Factor-?-Activated Primary Human Keratinocytes: Implications for Psoriasis and Inflammatory Skin Disease

    doi: 10.1038/jid.2008.122

    Figure Lengend Snippet: Effects of rapamycin on TNF-α-induced IκB degradation in primary human keratinocytes

    Article Snippet: TNF-α was obtained from R & D Systems (Minneapolis, MN).

    Techniques:

    Time course of hydrogen peroxide production induced by TNF-α in primary human keratinocytes

    Journal:

    Article Title: Reactive Oxygen Species in Tumor Necrosis Factor-?-Activated Primary Human Keratinocytes: Implications for Psoriasis and Inflammatory Skin Disease

    doi: 10.1038/jid.2008.122

    Figure Lengend Snippet: Time course of hydrogen peroxide production induced by TNF-α in primary human keratinocytes

    Article Snippet: TNF-α was obtained from R & D Systems (Minneapolis, MN).

    Techniques:

    The construction of human ALIM infected by Streptococcus . A. The relative LDH vitality of supernates in ALIM at 4 h, 24 h and 48 h. B. The relative expression of IL-6, IL-8 and TNF-α of supernates in ALIM. LDH, lactate

    Journal: Bioengineered

    Article Title: Effect and mechanism of calpains on pediatric lobar pneumonia

    doi: 10.1080/21655979.2016.1234544

    Figure Lengend Snippet: The construction of human ALIM infected by Streptococcus . A. The relative LDH vitality of supernates in ALIM at 4 h, 24 h and 48 h. B. The relative expression of IL-6, IL-8 and TNF-α of supernates in ALIM. LDH, lactate

    Article Snippet: Quantitative measurement of IL-6 (RAB0306), IL-8 (RAB0319), and TNF-α (RAB1089) in supernates of ALIM was performed based on the human ELISA kit instructions (Sigma, USA).

    Techniques: Infection, Expressing

    The effect of calpains on the lung cells MRC-5. A. The transfection efficiency of siRNA-calpains 1 and 2 to lung fibroblast MRC-5 cells. B. Expressions of IL-6, IL-8 and TNF-α in transferred lung cells with calpains silence. C. The expressions

    Journal: Bioengineered

    Article Title: Effect and mechanism of calpains on pediatric lobar pneumonia

    doi: 10.1080/21655979.2016.1234544

    Figure Lengend Snippet: The effect of calpains on the lung cells MRC-5. A. The transfection efficiency of siRNA-calpains 1 and 2 to lung fibroblast MRC-5 cells. B. Expressions of IL-6, IL-8 and TNF-α in transferred lung cells with calpains silence. C. The expressions

    Article Snippet: Quantitative measurement of IL-6 (RAB0306), IL-8 (RAB0319), and TNF-α (RAB1089) in supernates of ALIM was performed based on the human ELISA kit instructions (Sigma, USA).

    Techniques: Transfection

    TNF-α induces Bcl6 gene expression in the hepatocytes and Bcl6 overexpression upregulates the TNF-α levels in vivo . (A) The RNA levels of Tnf- α, Il-6, Il-12, Cxcl9, and Cxcl10 were examined by RT-qPCR in B6.2- and B6.2S-injected mouse liver isolated during the HBV clearance stage. (B) AML12 cells were treated with or without TNF-α (100 ng/ml) for the indicated time periods and Bcl6 RNA was analyzed by RT-qPCR. The induction fold means the ratio of the Bcl6 RNA levels in the presence of TNF-α over those without TNF-α. (C) AML12 and Huh-7 cells were transfected with 1 μg of vector or the Bcl6 -expressing plasmid. Two days later, the TNF-α RNA levels were analyzed by RT-qPCR analysis. (D) The liver RNA from the B6.2 or the (B6.2 + Bcl6 ) mice at 2 w.p.i. were analyzed for Tnf- α expression by RT-qPCR. In (A–D) , * P

    Journal: Frontiers in Microbiology

    Article Title: B-Cell Lymphoma 6 (BCL6) Is a Host Restriction Factor That Can Suppress HBV Gene Expression and Modulate Immune Responses

    doi: 10.3389/fmicb.2018.03253

    Figure Lengend Snippet: TNF-α induces Bcl6 gene expression in the hepatocytes and Bcl6 overexpression upregulates the TNF-α levels in vivo . (A) The RNA levels of Tnf- α, Il-6, Il-12, Cxcl9, and Cxcl10 were examined by RT-qPCR in B6.2- and B6.2S-injected mouse liver isolated during the HBV clearance stage. (B) AML12 cells were treated with or without TNF-α (100 ng/ml) for the indicated time periods and Bcl6 RNA was analyzed by RT-qPCR. The induction fold means the ratio of the Bcl6 RNA levels in the presence of TNF-α over those without TNF-α. (C) AML12 and Huh-7 cells were transfected with 1 μg of vector or the Bcl6 -expressing plasmid. Two days later, the TNF-α RNA levels were analyzed by RT-qPCR analysis. (D) The liver RNA from the B6.2 or the (B6.2 + Bcl6 ) mice at 2 w.p.i. were analyzed for Tnf- α expression by RT-qPCR. In (A–D) , * P

    Article Snippet: The cytokines used for stimulating Bcl6 expression or chemokine induction included TNF-α (315-01A, PeProtech, USA) and IFN-γ (485MI, R & D, USA).

    Techniques: Expressing, Over Expression, In Vivo, Quantitative RT-PCR, Injection, Isolation, Transfection, Plasmid Preparation, Mouse Assay

    BCL6 expression synergizes TNF-α-induced Cxcl9/Cxcl10 expression and enhances immune cell infiltration into the liver. (A,B) AML12 cells, (C) Huh-7 cells, were transfected with 1 μg of vector or the Bcl6 -expressing plasmid. Two days later, the cells were treated with or without (A,C) TNF-α (100 ng/ml) or (B) IFN-γ (50 ng/ml) for 3 h. RNA was extracted and analyzed for Cxcl9/Cxcl10 expression by RT-qPCR. (D) The liver RNA from the B6.2 or the (B6.2 + Bcl6 ) mice at 2 w.p.i. were analyzed for Cxcl9/Cxcl10 expression by RT-qPCR and (E) the liver tissues were analyzed by hematoxylin eosin staining. The arrows indicate the infiltrating immune cells. The images are displayed at 400X magnification. The average number of infiltrating foci were obtained from 15 different fields for each mouse ( N = 5) at 200X magnification and presented as the mean ± SD . LPF, low power field. * P

    Journal: Frontiers in Microbiology

    Article Title: B-Cell Lymphoma 6 (BCL6) Is a Host Restriction Factor That Can Suppress HBV Gene Expression and Modulate Immune Responses

    doi: 10.3389/fmicb.2018.03253

    Figure Lengend Snippet: BCL6 expression synergizes TNF-α-induced Cxcl9/Cxcl10 expression and enhances immune cell infiltration into the liver. (A,B) AML12 cells, (C) Huh-7 cells, were transfected with 1 μg of vector or the Bcl6 -expressing plasmid. Two days later, the cells were treated with or without (A,C) TNF-α (100 ng/ml) or (B) IFN-γ (50 ng/ml) for 3 h. RNA was extracted and analyzed for Cxcl9/Cxcl10 expression by RT-qPCR. (D) The liver RNA from the B6.2 or the (B6.2 + Bcl6 ) mice at 2 w.p.i. were analyzed for Cxcl9/Cxcl10 expression by RT-qPCR and (E) the liver tissues were analyzed by hematoxylin eosin staining. The arrows indicate the infiltrating immune cells. The images are displayed at 400X magnification. The average number of infiltrating foci were obtained from 15 different fields for each mouse ( N = 5) at 200X magnification and presented as the mean ± SD . LPF, low power field. * P

    Article Snippet: The cytokines used for stimulating Bcl6 expression or chemokine induction included TNF-α (315-01A, PeProtech, USA) and IFN-γ (485MI, R & D, USA).

    Techniques: Expressing, Transfection, Plasmid Preparation, Quantitative RT-PCR, Mouse Assay, Staining

    Working model for the induction and anti-HBV activity of BCL6 in vivo ), followed by infiltration of many other immune cells. (2) These immune cells produce diverse cytokines in the liver. (3) The inflammatory cytokines such as TNF-α can upregulate Bcl6 expression. (4) BCL6 can repress HBV promoter activity, and (5) meanwhile synergizes TNF-α signaling to produce large amounts of CXCL9/CXCL10 chemokines. (6) The chemokines recruit more immune cells infiltrating to the livers and (7) produce higher levels of cytokines and chemokines. These immune cells, cytokines together with the BCL6 functions may ultimately lead to HBV clearance.

    Journal: Frontiers in Microbiology

    Article Title: B-Cell Lymphoma 6 (BCL6) Is a Host Restriction Factor That Can Suppress HBV Gene Expression and Modulate Immune Responses

    doi: 10.3389/fmicb.2018.03253

    Figure Lengend Snippet: Working model for the induction and anti-HBV activity of BCL6 in vivo ), followed by infiltration of many other immune cells. (2) These immune cells produce diverse cytokines in the liver. (3) The inflammatory cytokines such as TNF-α can upregulate Bcl6 expression. (4) BCL6 can repress HBV promoter activity, and (5) meanwhile synergizes TNF-α signaling to produce large amounts of CXCL9/CXCL10 chemokines. (6) The chemokines recruit more immune cells infiltrating to the livers and (7) produce higher levels of cytokines and chemokines. These immune cells, cytokines together with the BCL6 functions may ultimately lead to HBV clearance.

    Article Snippet: The cytokines used for stimulating Bcl6 expression or chemokine induction included TNF-α (315-01A, PeProtech, USA) and IFN-γ (485MI, R & D, USA).

    Techniques: Activity Assay, In Vivo, Expressing