fas‑associated death domain Search Results


fas protein  (Shanghai Korain Biotech Co Ltd)
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death domain fadd  (Boster Bio)
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Death Domain Fadd, 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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rabbit anti rat runx2 monoclonal antibodies  (Boster Bio)
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fas  (Boster Bio)
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Primer sequences and Tm for RT-qPCR.
Fas, 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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rabbit anti cleaved caspase 1  (Boster Bio)
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Primer sequences and Tm for RT-qPCR.
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fadd  (Boster Bio)
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Fig. 2. Scutellarein treatment activated the intrinsic apoptosis pathway in multiple myeloma cells in vitro. A–C, analysis <t>of</t> <t>caspase-9,</t> -8 and -3 activities in IM-9, MM.1R or viable circulating B lymphocytes (CBL) after treatment with indicated concentrations of scutellarein for 24 h. Caspase activity was measured by the relative fluorescent units (RFU) of cleaved substrates. Data was normalized to the vehicle-treated CBL group. D–I, influence of <t>FADD</t> or APAF1 knockdown on the apoptosis- inducing effect of 400 μg/ml scutellarein treatment for 24 h. shRNA targeting green fluorescent protein gene (sh-NC) was used as negative control for FADD or APAF1 knockdown. Data in DeI were normalized to the un-transfected group (WT) in each cell line. *, p < 0.05; **, p < 0.01; ***, p < 0.001; ****, p < 0.0001.
Fadd, 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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rabbit anti-fas-associated death domain protein (fadd  (ZenBio)
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ZenBio rabbit anti-fas-associated death domain protein (fadd
Fig. 2. Scutellarein treatment activated the intrinsic apoptosis pathway in multiple myeloma cells in vitro. A–C, analysis <t>of</t> <t>caspase-9,</t> -8 and -3 activities in IM-9, MM.1R or viable circulating B lymphocytes (CBL) after treatment with indicated concentrations of scutellarein for 24 h. Caspase activity was measured by the relative fluorescent units (RFU) of cleaved substrates. Data was normalized to the vehicle-treated CBL group. D–I, influence of <t>FADD</t> or APAF1 knockdown on the apoptosis- inducing effect of 400 μg/ml scutellarein treatment for 24 h. shRNA targeting green fluorescent protein gene (sh-NC) was used as negative control for FADD or APAF1 knockdown. Data in DeI were normalized to the un-transfected group (WT) in each cell line. *, p < 0.05; **, p < 0.01; ***, p < 0.001; ****, p < 0.0001.
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adapter protein fas-associated protein death domain (fadd)  (Medema labs)
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Fig. 2. Scutellarein treatment activated the intrinsic apoptosis pathway in multiple myeloma cells in vitro. A–C, analysis <t>of</t> <t>caspase-9,</t> -8 and -3 activities in IM-9, MM.1R or viable circulating B lymphocytes (CBL) after treatment with indicated concentrations of scutellarein for 24 h. Caspase activity was measured by the relative fluorescent units (RFU) of cleaved substrates. Data was normalized to the vehicle-treated CBL group. D–I, influence of <t>FADD</t> or APAF1 knockdown on the apoptosis- inducing effect of 400 μg/ml scutellarein treatment for 24 h. shRNA targeting green fluorescent protein gene (sh-NC) was used as negative control for FADD or APAF1 knockdown. Data in DeI were normalized to the un-transfected group (WT) in each cell line. *, p < 0.05; **, p < 0.01; ***, p < 0.001; ****, p < 0.0001.
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fas‑associated death domain  (Beijing Solarbio Science)
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Beijing Solarbio Science fas‑associated death domain
Fig. 2. Scutellarein treatment activated the intrinsic apoptosis pathway in multiple myeloma cells in vitro. A–C, analysis <t>of</t> <t>caspase-9,</t> -8 and -3 activities in IM-9, MM.1R or viable circulating B lymphocytes (CBL) after treatment with indicated concentrations of scutellarein for 24 h. Caspase activity was measured by the relative fluorescent units (RFU) of cleaved substrates. Data was normalized to the vehicle-treated CBL group. D–I, influence of <t>FADD</t> or APAF1 knockdown on the apoptosis- inducing effect of 400 μg/ml scutellarein treatment for 24 h. shRNA targeting green fluorescent protein gene (sh-NC) was used as negative control for FADD or APAF1 knockdown. Data in DeI were normalized to the un-transfected group (WT) in each cell line. *, p < 0.05; **, p < 0.01; ***, p < 0.001; ****, p < 0.0001.
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anti-human fas-associated protein death domain (fadd) (if7  (Enzo Biochem)
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Fig. 2. Scutellarein treatment activated the intrinsic apoptosis pathway in multiple myeloma cells in vitro. A–C, analysis <t>of</t> <t>caspase-9,</t> -8 and -3 activities in IM-9, MM.1R or viable circulating B lymphocytes (CBL) after treatment with indicated concentrations of scutellarein for 24 h. Caspase activity was measured by the relative fluorescent units (RFU) of cleaved substrates. Data was normalized to the vehicle-treated CBL group. D–I, influence of <t>FADD</t> or APAF1 knockdown on the apoptosis- inducing effect of 400 μg/ml scutellarein treatment for 24 h. shRNA targeting green fluorescent protein gene (sh-NC) was used as negative control for FADD or APAF1 knockdown. Data in DeI were normalized to the un-transfected group (WT) in each cell line. *, p < 0.05; **, p < 0.01; ***, p < 0.001; ****, p < 0.0001.
Anti Human Fas Associated Protein Death Domain (Fadd) (If7, 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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fas-associated death domain (fadd)  (Medema labs)
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Medema labs fas-associated death domain (fadd)
Fig. 2. Scutellarein treatment activated the intrinsic apoptosis pathway in multiple myeloma cells in vitro. A–C, analysis <t>of</t> <t>caspase-9,</t> -8 and -3 activities in IM-9, MM.1R or viable circulating B lymphocytes (CBL) after treatment with indicated concentrations of scutellarein for 24 h. Caspase activity was measured by the relative fluorescent units (RFU) of cleaved substrates. Data was normalized to the vehicle-treated CBL group. D–I, influence of <t>FADD</t> or APAF1 knockdown on the apoptosis- inducing effect of 400 μg/ml scutellarein treatment for 24 h. shRNA targeting green fluorescent protein gene (sh-NC) was used as negative control for FADD or APAF1 knockdown. Data in DeI were normalized to the un-transfected group (WT) in each cell line. *, p < 0.05; **, p < 0.01; ***, p < 0.001; ****, p < 0.0001.
Fas Associated Death Domain (Fadd), supplied by Medema labs, 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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fas-associated death domain tumor necrosis factor receptor–associated death domain  (Becton Dickinson)
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Fig. 2. Scutellarein treatment activated the intrinsic apoptosis pathway in multiple myeloma cells in vitro. A–C, analysis <t>of</t> <t>caspase-9,</t> -8 and -3 activities in IM-9, MM.1R or viable circulating B lymphocytes (CBL) after treatment with indicated concentrations of scutellarein for 24 h. Caspase activity was measured by the relative fluorescent units (RFU) of cleaved substrates. Data was normalized to the vehicle-treated CBL group. D–I, influence of <t>FADD</t> or APAF1 knockdown on the apoptosis- inducing effect of 400 μg/ml scutellarein treatment for 24 h. shRNA targeting green fluorescent protein gene (sh-NC) was used as negative control for FADD or APAF1 knockdown. Data in DeI were normalized to the un-transfected group (WT) in each cell line. *, p < 0.05; **, p < 0.01; ***, p < 0.001; ****, p < 0.0001.
Fas Associated Death Domain Tumor Necrosis Factor Receptor–Associated Death Domain, 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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Image Search Results


Primer sequences and Tm for RT-qPCR.

Journal: BioMed Research International

Article Title: Role of the Death Receptor and Endoplasmic Reticulum Stress Signaling Pathways in Polyphyllin I-Regulated Apoptosis of Human Hepatocellular Carcinoma HepG2 Cells

doi: 10.1155/2018/5241941

Figure Lengend Snippet: Primer sequences and Tm for RT-qPCR.

Article Snippet: The primary antibodies included B-cell lymphoma 2 (Bcl-2), Bcl-2-associated X (Bax), IRE-1, FAS associated via death domain (FADD), FAS, β -actin (Wuhan Boster Biological Technology, Ltd.,), TNF- α , CHOP and caspase-12 (BIOSS, Beijing, China) at 1:500 dilution and Cleaved-caspase3 (Cell Signaling Technology, Inc., Danvers, MA, USA), cleaved-caspase8 (Beyotime Institute of Biotechnology, Shanghai, China) at 1:1 000 dilution.

Techniques: Sequencing

Fig. 2. Scutellarein treatment activated the intrinsic apoptosis pathway in multiple myeloma cells in vitro. A–C, analysis of caspase-9, -8 and -3 activities in IM-9, MM.1R or viable circulating B lymphocytes (CBL) after treatment with indicated concentrations of scutellarein for 24 h. Caspase activity was measured by the relative fluorescent units (RFU) of cleaved substrates. Data was normalized to the vehicle-treated CBL group. D–I, influence of FADD or APAF1 knockdown on the apoptosis- inducing effect of 400 μg/ml scutellarein treatment for 24 h. shRNA targeting green fluorescent protein gene (sh-NC) was used as negative control for FADD or APAF1 knockdown. Data in DeI were normalized to the un-transfected group (WT) in each cell line. *, p < 0.05; **, p < 0.01; ***, p < 0.001; ****, p < 0.0001.

Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

Article Title: Scutellarein selectively targets multiple myeloma cells by increasing mitochondrial superoxide production and activating intrinsic apoptosis pathway.

doi: 10.1016/j.biopha.2018.09.024

Figure Lengend Snippet: Fig. 2. Scutellarein treatment activated the intrinsic apoptosis pathway in multiple myeloma cells in vitro. A–C, analysis of caspase-9, -8 and -3 activities in IM-9, MM.1R or viable circulating B lymphocytes (CBL) after treatment with indicated concentrations of scutellarein for 24 h. Caspase activity was measured by the relative fluorescent units (RFU) of cleaved substrates. Data was normalized to the vehicle-treated CBL group. D–I, influence of FADD or APAF1 knockdown on the apoptosis- inducing effect of 400 μg/ml scutellarein treatment for 24 h. shRNA targeting green fluorescent protein gene (sh-NC) was used as negative control for FADD or APAF1 knockdown. Data in DeI were normalized to the un-transfected group (WT) in each cell line. *, p < 0.05; **, p < 0.01; ***, p < 0.001; ****, p < 0.0001.

Article Snippet: Antibodies for detecting FADD (PA1464, BosterBio, Pleasanton, USA), Apaf-1 (PA1249-1, BosterBio), active Caspase-3 (269518, Novus Biologicals, Littleton, USA) Bax (AF820, R& D Systems, Minneapolis, USA), Bcl-2 (RP1003, BosterBio) and GAPDH (HPA040067, Atlas Antibodies, Bromma, Sweden) were applied following manufacturer’s instructions.

Techniques: In Vitro, Activity Assay, Knockdown, shRNA, Negative Control, Transfection