anti flip antibody Search Results


mouse anti human monoclonal antibody  (Boster Bio)
91
Boster Bio mouse anti human monoclonal antibody
Mouse Anti Human Monoclonal Antibody, supplied by Boster Bio, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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anti ar mouse monoclonal antibody  (Boster Bio)
90
Boster Bio anti ar mouse monoclonal antibody
Anti Ar Mouse Monoclonal Antibody, supplied by Boster Bio, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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anti–c-flip antibody  (Merck KGaA)
90
Merck KGaA anti–c-flip antibody
Anti–C Flip Antibody, supplied by Merck KGaA, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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secondary antibody goat flip anti-rabbit  (abberior instruments)
90
abberior instruments secondary antibody goat flip anti-rabbit
Secondary Antibody Goat Flip Anti Rabbit, supplied by abberior instruments, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mouse monoclonal anti-flip antibody (nf6  (Enzo Biochem)
90
Enzo Biochem mouse monoclonal anti-flip antibody (nf6
Mouse Monoclonal Anti Flip Antibody (Nf6, supplied by Enzo Biochem, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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monoclonal antibody against flip (dave-2  (Enzo Biochem)
90
Enzo Biochem monoclonal antibody against flip (dave-2
Analysis of apoptosis-regulatory proteins of the death receptor pathway in single-walled carbon nanotubes (SWCNT)-transformed cells. a, Passage-control BEAS-2B and transformed B-SWCNT cell lysates were prepared and analyzed for <t>c-FLIP,</t> TNFR1, and FasR by Western blotting. b, Subconfluent monolayers of SWCNT-transformed cells were treated with TNF-α (0–100 ng/ml) or FasL (0–50 ng/ml) in the presence or absence of <t>c-FLIP</t> <t>inhibitor</t> 5809354 (5 μM) for 12 h, after which they were analyzed for apoptosis by Hoechst 33342 assay. c, Knockdown of c-FLIP in SWCNT-transformed cells using shRNA lentiviral particles. The expression level of c-FLIP in shRNA control (shCon) and knockdown (shFLIP) B-SWCNT cells was determined by Western blotting using specific antibody against c-FLIP. d, shCon and shFLIP cells were treated with TNF-α (0–100 ng/ml) or FasL (0–50 ng/ml), and analyzed for apoptosis by Hoechst 33342 assay at 12 h post-treatment. Data are means ± SD (n = 4). *P ≤ .05 versus control cells.
Monoclonal Antibody Against Flip (Dave 2, supplied by Enzo Biochem, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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monoclonal antibody against flip (dave-2 - by Bioz Stars, 2026-02
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mouse igg1-κ, mopc-21  (Merck & Co)
90
Merck & Co mouse igg1-κ, mopc-21
Analysis of apoptosis-regulatory proteins of the death receptor pathway in single-walled carbon nanotubes (SWCNT)-transformed cells. a, Passage-control BEAS-2B and transformed B-SWCNT cell lysates were prepared and analyzed for <t>c-FLIP,</t> TNFR1, and FasR by Western blotting. b, Subconfluent monolayers of SWCNT-transformed cells were treated with TNF-α (0–100 ng/ml) or FasL (0–50 ng/ml) in the presence or absence of <t>c-FLIP</t> <t>inhibitor</t> 5809354 (5 μM) for 12 h, after which they were analyzed for apoptosis by Hoechst 33342 assay. c, Knockdown of c-FLIP in SWCNT-transformed cells using shRNA lentiviral particles. The expression level of c-FLIP in shRNA control (shCon) and knockdown (shFLIP) B-SWCNT cells was determined by Western blotting using specific antibody against c-FLIP. d, shCon and shFLIP cells were treated with TNF-α (0–100 ng/ml) or FasL (0–50 ng/ml), and analyzed for apoptosis by Hoechst 33342 assay at 12 h post-treatment. Data are means ± SD (n = 4). *P ≤ .05 versus control cells.
Mouse Igg1 κ, Mopc 21, supplied by Merck & Co, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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polyclonal rabbit-anti-flip  (Becton Dickinson)
90
Becton Dickinson polyclonal rabbit-anti-flip
Analysis of apoptosis-regulatory proteins of the death receptor pathway in single-walled carbon nanotubes (SWCNT)-transformed cells. a, Passage-control BEAS-2B and transformed B-SWCNT cell lysates were prepared and analyzed for <t>c-FLIP,</t> TNFR1, and FasR by Western blotting. b, Subconfluent monolayers of SWCNT-transformed cells were treated with TNF-α (0–100 ng/ml) or FasL (0–50 ng/ml) in the presence or absence of <t>c-FLIP</t> <t>inhibitor</t> 5809354 (5 μM) for 12 h, after which they were analyzed for apoptosis by Hoechst 33342 assay. c, Knockdown of c-FLIP in SWCNT-transformed cells using shRNA lentiviral particles. The expression level of c-FLIP in shRNA control (shCon) and knockdown (shFLIP) B-SWCNT cells was determined by Western blotting using specific antibody against c-FLIP. d, shCon and shFLIP cells were treated with TNF-α (0–100 ng/ml) or FasL (0–50 ng/ml), and analyzed for apoptosis by Hoechst 33342 assay at 12 h post-treatment. Data are means ± SD (n = 4). *P ≤ .05 versus control cells.
Polyclonal Rabbit Anti Flip, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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rabbit anti-c-flip polyclonal antibody  (MBL Life science)
90
MBL Life science rabbit anti-c-flip polyclonal antibody
Analysis of apoptosis-regulatory proteins of the death receptor pathway in single-walled carbon nanotubes (SWCNT)-transformed cells. a, Passage-control BEAS-2B and transformed B-SWCNT cell lysates were prepared and analyzed for <t>c-FLIP,</t> TNFR1, and FasR by Western blotting. b, Subconfluent monolayers of SWCNT-transformed cells were treated with TNF-α (0–100 ng/ml) or FasL (0–50 ng/ml) in the presence or absence of <t>c-FLIP</t> <t>inhibitor</t> 5809354 (5 μM) for 12 h, after which they were analyzed for apoptosis by Hoechst 33342 assay. c, Knockdown of c-FLIP in SWCNT-transformed cells using shRNA lentiviral particles. The expression level of c-FLIP in shRNA control (shCon) and knockdown (shFLIP) B-SWCNT cells was determined by Western blotting using specific antibody against c-FLIP. d, shCon and shFLIP cells were treated with TNF-α (0–100 ng/ml) or FasL (0–50 ng/ml), and analyzed for apoptosis by Hoechst 33342 assay at 12 h post-treatment. Data are means ± SD (n = 4). *P ≤ .05 versus control cells.
Rabbit Anti C Flip Polyclonal Antibody, supplied by MBL Life science, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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mouse anti-flip monoclonal antibody  (Becton Dickinson)
90
Becton Dickinson mouse anti-flip monoclonal antibody
Analysis of apoptosis-regulatory proteins of the death receptor pathway in single-walled carbon nanotubes (SWCNT)-transformed cells. a, Passage-control BEAS-2B and transformed B-SWCNT cell lysates were prepared and analyzed for <t>c-FLIP,</t> TNFR1, and FasR by Western blotting. b, Subconfluent monolayers of SWCNT-transformed cells were treated with TNF-α (0–100 ng/ml) or FasL (0–50 ng/ml) in the presence or absence of <t>c-FLIP</t> <t>inhibitor</t> 5809354 (5 μM) for 12 h, after which they were analyzed for apoptosis by Hoechst 33342 assay. c, Knockdown of c-FLIP in SWCNT-transformed cells using shRNA lentiviral particles. The expression level of c-FLIP in shRNA control (shCon) and knockdown (shFLIP) B-SWCNT cells was determined by Western blotting using specific antibody against c-FLIP. d, shCon and shFLIP cells were treated with TNF-α (0–100 ng/ml) or FasL (0–50 ng/ml), and analyzed for apoptosis by Hoechst 33342 assay at 12 h post-treatment. Data are means ± SD (n = 4). *P ≤ .05 versus control cells.
Mouse Anti Flip Monoclonal Antibody, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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anti-c-flip antibody  (Amersham Pharmacia Biotech Ltd)
90
Amersham Pharmacia Biotech Ltd anti-c-flip antibody
Analysis of apoptosis-regulatory proteins of the death receptor pathway in single-walled carbon nanotubes (SWCNT)-transformed cells. a, Passage-control BEAS-2B and transformed B-SWCNT cell lysates were prepared and analyzed for <t>c-FLIP,</t> TNFR1, and FasR by Western blotting. b, Subconfluent monolayers of SWCNT-transformed cells were treated with TNF-α (0–100 ng/ml) or FasL (0–50 ng/ml) in the presence or absence of <t>c-FLIP</t> <t>inhibitor</t> 5809354 (5 μM) for 12 h, after which they were analyzed for apoptosis by Hoechst 33342 assay. c, Knockdown of c-FLIP in SWCNT-transformed cells using shRNA lentiviral particles. The expression level of c-FLIP in shRNA control (shCon) and knockdown (shFLIP) B-SWCNT cells was determined by Western blotting using specific antibody against c-FLIP. d, shCon and shFLIP cells were treated with TNF-α (0–100 ng/ml) or FasL (0–50 ng/ml), and analyzed for apoptosis by Hoechst 33342 assay at 12 h post-treatment. Data are means ± SD (n = 4). *P ≤ .05 versus control cells.
Anti C Flip Antibody, supplied by Amersham Pharmacia Biotech Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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rabbit anti-human c-flip polyclonal antibodies  (Abcan Audio Visual Inc)
90
Abcan Audio Visual Inc rabbit anti-human c-flip polyclonal antibodies
Analysis of apoptosis-regulatory proteins of the death receptor pathway in single-walled carbon nanotubes (SWCNT)-transformed cells. a, Passage-control BEAS-2B and transformed B-SWCNT cell lysates were prepared and analyzed for <t>c-FLIP,</t> TNFR1, and FasR by Western blotting. b, Subconfluent monolayers of SWCNT-transformed cells were treated with TNF-α (0–100 ng/ml) or FasL (0–50 ng/ml) in the presence or absence of <t>c-FLIP</t> <t>inhibitor</t> 5809354 (5 μM) for 12 h, after which they were analyzed for apoptosis by Hoechst 33342 assay. c, Knockdown of c-FLIP in SWCNT-transformed cells using shRNA lentiviral particles. The expression level of c-FLIP in shRNA control (shCon) and knockdown (shFLIP) B-SWCNT cells was determined by Western blotting using specific antibody against c-FLIP. d, shCon and shFLIP cells were treated with TNF-α (0–100 ng/ml) or FasL (0–50 ng/ml), and analyzed for apoptosis by Hoechst 33342 assay at 12 h post-treatment. Data are means ± SD (n = 4). *P ≤ .05 versus control cells.
Rabbit Anti Human C Flip Polyclonal Antibodies, supplied by Abcan Audio Visual Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Analysis of apoptosis-regulatory proteins of the death receptor pathway in single-walled carbon nanotubes (SWCNT)-transformed cells. a, Passage-control BEAS-2B and transformed B-SWCNT cell lysates were prepared and analyzed for c-FLIP, TNFR1, and FasR by Western blotting. b, Subconfluent monolayers of SWCNT-transformed cells were treated with TNF-α (0–100 ng/ml) or FasL (0–50 ng/ml) in the presence or absence of c-FLIP inhibitor 5809354 (5 μM) for 12 h, after which they were analyzed for apoptosis by Hoechst 33342 assay. c, Knockdown of c-FLIP in SWCNT-transformed cells using shRNA lentiviral particles. The expression level of c-FLIP in shRNA control (shCon) and knockdown (shFLIP) B-SWCNT cells was determined by Western blotting using specific antibody against c-FLIP. d, shCon and shFLIP cells were treated with TNF-α (0–100 ng/ml) or FasL (0–50 ng/ml), and analyzed for apoptosis by Hoechst 33342 assay at 12 h post-treatment. Data are means ± SD (n = 4). *P ≤ .05 versus control cells.

Journal: Toxicological Sciences

Article Title: Carbon Nanotubes Induce Apoptosis Resistance of Human Lung Epithelial Cells Through FLICE-Inhibitory Protein

doi: 10.1093/toxsci/kfu251

Figure Lengend Snippet: Analysis of apoptosis-regulatory proteins of the death receptor pathway in single-walled carbon nanotubes (SWCNT)-transformed cells. a, Passage-control BEAS-2B and transformed B-SWCNT cell lysates were prepared and analyzed for c-FLIP, TNFR1, and FasR by Western blotting. b, Subconfluent monolayers of SWCNT-transformed cells were treated with TNF-α (0–100 ng/ml) or FasL (0–50 ng/ml) in the presence or absence of c-FLIP inhibitor 5809354 (5 μM) for 12 h, after which they were analyzed for apoptosis by Hoechst 33342 assay. c, Knockdown of c-FLIP in SWCNT-transformed cells using shRNA lentiviral particles. The expression level of c-FLIP in shRNA control (shCon) and knockdown (shFLIP) B-SWCNT cells was determined by Western blotting using specific antibody against c-FLIP. d, shCon and shFLIP cells were treated with TNF-α (0–100 ng/ml) or FasL (0–50 ng/ml), and analyzed for apoptosis by Hoechst 33342 assay at 12 h post-treatment. Data are means ± SD (n = 4). *P ≤ .05 versus control cells.

Article Snippet: Caspase-8 fluorometric substrate (IETD-AFC), caspase-9 fluorometric substrate (LEHD-AFC), caspase-8 inhibitor (z-IETD-FMK), caspase-9 inhibitor (z-LEHD-FMK), pan-caspase inhibitor (z-VAD-FMK), recombinant FasL ( Super FasLigand), tumor necrosis factor, and monoclonal antibody against FLIP (Dave-2) were obtained from Alexis Biochemicals (San Diego, CA).

Techniques: Transformation Assay, Western Blot, shRNA, Expressing

Apoptosis resistance signaling in single-walled carbon nanotubes (SWCNT)-transformed cells. a, Top-ranked cell death functions in whole genome signature included apoptosis in both epithelial and tumor cell lines. †predicted inhibition (Z = −2.2). Apoptosis in epithelial cell lines possessed a trend for predicted inhibition (Z = −1.96). b, Simulation of c-FLIP (CFLAR)-mediated apoptosis resistance during TNF/FasL exposure in the apoptotic canonical signaling pathway. Both differential gene expression (≥±2-fold and t-test) and prediction signaling (Z ≥ ±2) are shown.

Journal: Toxicological Sciences

Article Title: Carbon Nanotubes Induce Apoptosis Resistance of Human Lung Epithelial Cells Through FLICE-Inhibitory Protein

doi: 10.1093/toxsci/kfu251

Figure Lengend Snippet: Apoptosis resistance signaling in single-walled carbon nanotubes (SWCNT)-transformed cells. a, Top-ranked cell death functions in whole genome signature included apoptosis in both epithelial and tumor cell lines. †predicted inhibition (Z = −2.2). Apoptosis in epithelial cell lines possessed a trend for predicted inhibition (Z = −1.96). b, Simulation of c-FLIP (CFLAR)-mediated apoptosis resistance during TNF/FasL exposure in the apoptotic canonical signaling pathway. Both differential gene expression (≥±2-fold and t-test) and prediction signaling (Z ≥ ±2) are shown.

Article Snippet: Caspase-8 fluorometric substrate (IETD-AFC), caspase-9 fluorometric substrate (LEHD-AFC), caspase-8 inhibitor (z-IETD-FMK), caspase-9 inhibitor (z-LEHD-FMK), pan-caspase inhibitor (z-VAD-FMK), recombinant FasL ( Super FasLigand), tumor necrosis factor, and monoclonal antibody against FLIP (Dave-2) were obtained from Alexis Biochemicals (San Diego, CA).

Techniques: Transformation Assay, Inhibition, Expressing