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tradd  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology tradd
    Tradd, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 112 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+tradd/TRADD+Antibody/pm41421355-295-65-66
    Average 93 stars, based on 112 article reviews
    tradd - by Bioz Stars, 2026-10
    93/100 stars

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    Related Articles

    Western Blot:

    Article Title: Rubiarbonol B induces RIPK1-dependent necroptosis via NOX1-derived ROS production
    Article Snippet: .. Antibodies and reagents All commercial antibodies and chemicals were purchased from the following resources: anti-caspase-8 (#9746 ), anti-caspase-3 (#9662), anti-Bid (#2002), anti-Bcl-2 (#2872), anti-Bcl-xL (#2762), anti-RIPK3 (#13526, for WB and IP), anti-phospho-RIPK3-S227 (#93654), anti-phospho-MLKL-S358 (#37333), antiphospho-RIPK1-S166 (#65746), anti-phospho-IKKα/β-S176/180 (#2697), anti- IκBα (#9242), and antiphospho-p65-S536 (#3033) antibodies were from Cell Signaling Technology (Beverly, MA, USA); anti-FADD (sc-5559), anti-Mox1 (sc-518023), anti-TRADD (sc-46653), and anti-TNFR1 (sc-8436) antibodies were from Santa Cruz Biotechnology (Santa Cruz, CA, USA); anti-Actin antibody (A2066), anti-Flag antibody (F7425), Carbonyl cyanide 3-chlorophenylhydrazone (CCCP), Cycloheximide (CHX), Dihydroethidium (DHE), MitoTEMPO, Apocynin, Diphenyleneiodonium (DPI), Butylated hydroxyanisole (BHA), Necrostatin-1 (Nec-1), and Necrosulfonamide (NSA) were from Sigma-Aldrich (St. Louis, MO, USA); MitoTracker Green and MitoSox Red were from Invitrogen (Franklin, MA, USA); anti-PARP (556362) and anti-RIPK1 (556395) antibodies were from BD Biosciences (San Diego, CA, USA); anti-MLKL (ab184718) antibody was from Abcam (Cambridge, MA, USA); recombinant TNF-α (410-MT) and anti-caspase-8 (AF-705, for IP), antiTNFR1 (AF-425, for IP) antibodies were from R&D system (Minneapolis, MN, USA); recombinant human TRAIL ligand (310-04) was from PeproTech (Rocky Hill, NJ, USA); SM-164, benzyloxy-carbonyl-Asp-(OMe)Glu-(OMe)-Val-Asp-(OMe)- uoromethyl ketone (z-DEVD-fmk), benzyloxy-carbonyl-Ile-Glu-(OMe)-Tyr-Asp(OMe)- uoromethyl ketone (z-IETD-fmk), arbobenzoxy-valyl-alanyl-aspartyl-[O-methyl]uoromethylketone (z-VAD-fmk), and GSK-872 were from MedChemExpress (Monmouth Junction, NJ, USA). ..

    Article Title: A novel format of TNF-α binding affibody molecule ameliorate coronary artery endothelial injury in a mouse model of Kawasaki disease.
    Article Snippet: Kawasaki disease (KD) is a disease characterized by systemic immune vasculitis that often involves coronary arteries and can result in long-term cardiovascular sequelae.. Different strategies for treatment of KD-and KDinduced coronary artery lesions are currently under investigation, including passive immunization with antiTNFα monoclonal antibodies (mAbs).. Herein, we examine the potential therapeutic capabilities of a novel type of TNFα-targeting agent based on an affibody molecule possessing fundamentally different properties than mAbs.

    Recombinant:

    Article Title: Rubiarbonol B induces RIPK1-dependent necroptosis via NOX1-derived ROS production
    Article Snippet: .. Antibodies and reagents All commercial antibodies and chemicals were purchased from the following resources: anti-caspase-8 (#9746 ), anti-caspase-3 (#9662), anti-Bid (#2002), anti-Bcl-2 (#2872), anti-Bcl-xL (#2762), anti-RIPK3 (#13526, for WB and IP), anti-phospho-RIPK3-S227 (#93654), anti-phospho-MLKL-S358 (#37333), antiphospho-RIPK1-S166 (#65746), anti-phospho-IKKα/β-S176/180 (#2697), anti- IκBα (#9242), and antiphospho-p65-S536 (#3033) antibodies were from Cell Signaling Technology (Beverly, MA, USA); anti-FADD (sc-5559), anti-Mox1 (sc-518023), anti-TRADD (sc-46653), and anti-TNFR1 (sc-8436) antibodies were from Santa Cruz Biotechnology (Santa Cruz, CA, USA); anti-Actin antibody (A2066), anti-Flag antibody (F7425), Carbonyl cyanide 3-chlorophenylhydrazone (CCCP), Cycloheximide (CHX), Dihydroethidium (DHE), MitoTEMPO, Apocynin, Diphenyleneiodonium (DPI), Butylated hydroxyanisole (BHA), Necrostatin-1 (Nec-1), and Necrosulfonamide (NSA) were from Sigma-Aldrich (St. Louis, MO, USA); MitoTracker Green and MitoSox Red were from Invitrogen (Franklin, MA, USA); anti-PARP (556362) and anti-RIPK1 (556395) antibodies were from BD Biosciences (San Diego, CA, USA); anti-MLKL (ab184718) antibody was from Abcam (Cambridge, MA, USA); recombinant TNF-α (410-MT) and anti-caspase-8 (AF-705, for IP), antiTNFR1 (AF-425, for IP) antibodies were from R&D system (Minneapolis, MN, USA); recombinant human TRAIL ligand (310-04) was from PeproTech (Rocky Hill, NJ, USA); SM-164, benzyloxy-carbonyl-Asp-(OMe)Glu-(OMe)-Val-Asp-(OMe)- uoromethyl ketone (z-DEVD-fmk), benzyloxy-carbonyl-Ile-Glu-(OMe)-Tyr-Asp(OMe)- uoromethyl ketone (z-IETD-fmk), arbobenzoxy-valyl-alanyl-aspartyl-[O-methyl]uoromethylketone (z-VAD-fmk), and GSK-872 were from MedChemExpress (Monmouth Junction, NJ, USA). ..

    Staining:

    Article Title: RIPK1 prevents TRADD-driven, but TNFR1 independent, apoptosis during development
    Article Snippet: .. Sections were then stained with anti-TRADD (Santa Cruz, sc-7868) and anti-FADD (Santa Cruz, sc-6036) overnight at 4 °C. ..

    other:

    Article Title: Polarity protein AF6 functions as a modulator of necroptosis by regulating ubiquitination of RIPK1 in liver diseases
    Article Snippet: Antibodies and other reagents were obtained as follows: anti-AF6 and anti-RIPK1(receptor-interacting serine/threonine kinase 1) antibodies from BD Transduction Laboratories; anti-pRIPK1(S166), anti-TNFR1(TNF receptor superfamily member 1A), anti-Hsp90(heat shock protein 90), and anti-GAPDH(glyceraldehyde-3-phosphate dehydrogenase) antibodies from Cell Signaling Technology; anti-pRIPK3(Ser232) (receptor-interacting serine/threonine kinase 3), anti-pMLKL(Ser345)(mixed lineage kinase domain-like pseudokinase), anti-MLKL and anti-CYLD(CYLD lysine 63 deubiquitinase) antibodies from abcam; anti-USP21, anti-FADD (Fas-associated via death domain), anti-TRAF2(TNF receptor-associated factor 2), and anti-TRADD(TNFRSF1A associated via death domain) antibodies from Santa Cruz Biotechnology; anti-A20(TNF alpha-induced protein 3) antibody from ABClonal; anti-RIPK3 from Prosci; and anti-actin antibody from Servicebio.

    Article Title: MK2 phosphorylation of RIPK1 regulates TNF-mediated cell death.
    Article Snippet: TNF is a master proinflammatory cytokine whose pathogenic role in inflammatory disorders can, in certain conditions, be attributed to RIPK1 kinase-dependent cell death.. Survival, however, is the default response of most cells to TNF stimulation, indicating that cell demise is normally actively repressed and that specific checkpoints must be turned off for cell death to proceed.. We identified RIPK1 as a direct substrate of MK2 in the TNFR1 signalling pathway.

    Immunoprecipitation:

    Article Title: Kv7.4 channel is a key regulator of vascular inflammation and remodeling in neointimal hyperplasia and abdominal aortic aneurysms.
    Article Snippet: Inflammation has recently emerged as an important contributor for cardiovascular disease development and participates pivotally in the development of neointimal hyperplasia and abdominal aortic aneurysms (AAA) formation.. Kv7.4/KCNQ4, a K channel, is one of the important regulators of vascular function but its role in vascular inflammation is unexplored.. Here, we showed that the expression of Kv7.4 channel was elevated in the neointima and AAA tissues from mice and humans.

    Incubation:

    Article Title: Kv7.4 channel is a key regulator of vascular inflammation and remodeling in neointimal hyperplasia and abdominal aortic aneurysms.
    Article Snippet: Inflammation has recently emerged as an important contributor for cardiovascular disease development and participates pivotally in the development of neointimal hyperplasia and abdominal aortic aneurysms (AAA) formation.. Kv7.4/KCNQ4, a K channel, is one of the important regulators of vascular function but its role in vascular inflammation is unexplored.. Here, we showed that the expression of Kv7.4 channel was elevated in the neointima and AAA tissues from mice and humans.

    Article Title: Structural and functional elucidation of NF-κB signaling by the p75 neurotrophin receptor through recruitment of TRADD
    Article Snippet: .. Cells were then incubated overnight at 4 °C with anti-p75 NTR (Promega; G323A; 1:300) and anti-TRADD (Santa Cruz; sc-46653; 1:500) antibodies in PBS supplemented with 3% BSA. .. The Duolink In Situ Proximity Ligation kit (Sigma; DUO92007) was used as per the manufacturer’s instructions with fluorophore-conjugated secondary antibody to recognize HA (Sigma; H3667, 1:250) included during the amplification step.



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    MAPK signaling pathway is significantly upregulated in porcine AF. ( A – H ) RT-qPCR analysis of mRNA expression levels of ASK1, <t>TRADD,</t> JUN, MKK7, <t>MKK4,</t> <t>JNK2,</t> JNK3, and TP53 in porcine HF and AF. ( I ) Healthy follicles of 3–5 mm were randomly assigned to the control group, H 2 O 2 treatment group, and selonsertib pretreatment group. ( J–P ) The expression levels of ASK1, TRADD, JUN, MKK4, JNK2, JNK3, and TP53 in the control group, H 2 O 2 treatment group, and selonsertib pretreatment group were detected by RT-qPCR. Data are presented as the mean ± SEM from a minimum of three independent biological replicates. Significance levels are indicated as follows: * p < 0.05, ** p < 0.01, and *** p < 0.001.
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    Image Search Results


    MAPK signaling pathway is significantly upregulated in porcine AF. ( A – H ) RT-qPCR analysis of mRNA expression levels of ASK1, TRADD, JUN, MKK7, MKK4, JNK2, JNK3, and TP53 in porcine HF and AF. ( I ) Healthy follicles of 3–5 mm were randomly assigned to the control group, H 2 O 2 treatment group, and selonsertib pretreatment group. ( J–P ) The expression levels of ASK1, TRADD, JUN, MKK4, JNK2, JNK3, and TP53 in the control group, H 2 O 2 treatment group, and selonsertib pretreatment group were detected by RT-qPCR. Data are presented as the mean ± SEM from a minimum of three independent biological replicates. Significance levels are indicated as follows: * p < 0.05, ** p < 0.01, and *** p < 0.001.

    Journal: Antioxidants

    Article Title: Oxidative Stress Triggers Porcine Ovarian Granulosa Cell Apoptosis Through MAPK Signaling

    doi: 10.3390/antiox14080978

    Figure Lengend Snippet: MAPK signaling pathway is significantly upregulated in porcine AF. ( A – H ) RT-qPCR analysis of mRNA expression levels of ASK1, TRADD, JUN, MKK7, MKK4, JNK2, JNK3, and TP53 in porcine HF and AF. ( I ) Healthy follicles of 3–5 mm were randomly assigned to the control group, H 2 O 2 treatment group, and selonsertib pretreatment group. ( J–P ) The expression levels of ASK1, TRADD, JUN, MKK4, JNK2, JNK3, and TP53 in the control group, H 2 O 2 treatment group, and selonsertib pretreatment group were detected by RT-qPCR. Data are presented as the mean ± SEM from a minimum of three independent biological replicates. Significance levels are indicated as follows: * p < 0.05, ** p < 0.01, and *** p < 0.001.

    Article Snippet: Antibodies against Phospho-JNK1-T183/Y185 + JNK2-T183/Y185 + JNK3-T221/Y223 Rabbit mAb (AP1451), JNK2 Rabbit pAb (A1251), TRADD Rabbit pAb (A18626), MAP2K4 Rabbit pAb (A21597), and Phospho-MAP2K4-S257/T261 Rabbit pAb (AP0541) were purchased from ABclonal.

    Techniques: Quantitative RT-PCR, Expressing, Control

    ASK1 inhibition protects mouse GCs from apoptotic cell death. ( A ) CCK-8 was used to detect the cell viability of the control group, H 2 O 2 treatment group, and selonsertib pretreatment group. ( B – K ) The expression levels of ASK1, TRADD, JUN, MKK4, JNK2, JNK3, TP53, CASP3, and BAX in the control group, H 2 O 2 treatment group, and selonsertib pretreatment group were detected by RT-qPCR. Data represented the mean ± SEM of at least three biological replicates. * p < 0.05; ** p < 0.01; *** p < 0.001; ns: not significant.

    Journal: Antioxidants

    Article Title: Oxidative Stress Triggers Porcine Ovarian Granulosa Cell Apoptosis Through MAPK Signaling

    doi: 10.3390/antiox14080978

    Figure Lengend Snippet: ASK1 inhibition protects mouse GCs from apoptotic cell death. ( A ) CCK-8 was used to detect the cell viability of the control group, H 2 O 2 treatment group, and selonsertib pretreatment group. ( B – K ) The expression levels of ASK1, TRADD, JUN, MKK4, JNK2, JNK3, TP53, CASP3, and BAX in the control group, H 2 O 2 treatment group, and selonsertib pretreatment group were detected by RT-qPCR. Data represented the mean ± SEM of at least three biological replicates. * p < 0.05; ** p < 0.01; *** p < 0.001; ns: not significant.

    Article Snippet: Antibodies against Phospho-JNK1-T183/Y185 + JNK2-T183/Y185 + JNK3-T221/Y223 Rabbit mAb (AP1451), JNK2 Rabbit pAb (A1251), TRADD Rabbit pAb (A18626), MAP2K4 Rabbit pAb (A21597), and Phospho-MAP2K4-S257/T261 Rabbit pAb (AP0541) were purchased from ABclonal.

    Techniques: Inhibition, CCK-8 Assay, Control, Expressing, Quantitative RT-PCR

    Inhibition of ASK1 rescued the apoptosis of GC. ( A – G ) Western blot was used to detect the expression levels of P-ASK1, TRADD, P-MKK4, JNK2, P-JNK1/2/3, and CL-CASP3 in the control group, H 2 O 2 treatment group, and selonsertib pretreatment group. ( H ) ROS staining is used to detect reactive oxygen species in the control group, H 2 O 2 treatment group, and selonsertib pretreatment group. ( I ) Mito Tracker staining is used to detect mitochondrial activity in the control group, H 2 O 2 treatment group, and selonsertib pretreatment group. Scale bars in ( H , I ) are 100 µm. Data are presented as the mean ± SEM from a minimum of three independent biological replicates. Significance levels are indicated as follows: * p < 0.05, ** p < 0.01, and *** p < 0.001.

    Journal: Antioxidants

    Article Title: Oxidative Stress Triggers Porcine Ovarian Granulosa Cell Apoptosis Through MAPK Signaling

    doi: 10.3390/antiox14080978

    Figure Lengend Snippet: Inhibition of ASK1 rescued the apoptosis of GC. ( A – G ) Western blot was used to detect the expression levels of P-ASK1, TRADD, P-MKK4, JNK2, P-JNK1/2/3, and CL-CASP3 in the control group, H 2 O 2 treatment group, and selonsertib pretreatment group. ( H ) ROS staining is used to detect reactive oxygen species in the control group, H 2 O 2 treatment group, and selonsertib pretreatment group. ( I ) Mito Tracker staining is used to detect mitochondrial activity in the control group, H 2 O 2 treatment group, and selonsertib pretreatment group. Scale bars in ( H , I ) are 100 µm. Data are presented as the mean ± SEM from a minimum of three independent biological replicates. Significance levels are indicated as follows: * p < 0.05, ** p < 0.01, and *** p < 0.001.

    Article Snippet: Antibodies against Phospho-JNK1-T183/Y185 + JNK2-T183/Y185 + JNK3-T221/Y223 Rabbit mAb (AP1451), JNK2 Rabbit pAb (A1251), TRADD Rabbit pAb (A18626), MAP2K4 Rabbit pAb (A21597), and Phospho-MAP2K4-S257/T261 Rabbit pAb (AP0541) were purchased from ABclonal.

    Techniques: Inhibition, Western Blot, Expressing, Control, Staining, Activity Assay