human reactive sting pathway antibody sampler kit Search Results


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Cell Signaling Technology Inc human reactive sting pathway antibody sampler kit cell signaling technology 38866 wb
Human Reactive Sting Pathway Antibody Sampler Kit Cell Signaling Technology 38866 Wb, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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human reactive sting pathway antibody sampler kit cell signaling technology 38866 wb - by Bioz Stars, 2026-04
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Cell Signaling Technology Inc autophagy antibody sampler kit
MT1H induces p53-dependent <t>autophagy</t> via regulating the key genes in nutrient transportation. (A) Semi-qPCR to verify the downregulated or upregulated genes by MT1H in AGS cells. AGS-tetO-MT1H cells were treated with Dox (2 µg/ml) to induce the expression of ectopic MT1H. 24 h later, cells were harvested for total RNA extraction and reverse transcription followed by semi-qPCR. (B) The cells expressing tetO-MT1H were treated with Dox (2 µg/ml) to induce the expression of ectopic MT1H. 24 h later, cells were harvested for immunoblot analysis with indicated <t>antibodies.</t> NE-PER Nuclear and Cytoplasmic Extraction <t>kit</t> (Thermo) was used to fractionate cells into cytosol compartment and nuclear compartment. (C) MT1H biological functions by KEGG analysis. The participation in mineral absorption was predicted by KEGG-Pathway (https://www.genome.jp/kegg/). (D) Illustrative diagram of MT1H biological functions in gastric cells. The information in the diagram is the combination of our current research and KEGG-Pathway.
Autophagy Antibody Sampler Kit, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/autophagy antibody sampler kit/product/Cell Signaling Technology Inc
Average 94 stars, based on 1 article reviews
autophagy antibody sampler kit - by Bioz Stars, 2026-04
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Cell Signaling Technology Inc human reactive inflammasome antibody sampler kit ii
Fig. 5. Inhibition of PA-NLRP3 <t>inflammasome</t> axis-induced inflammation and ECM degradation by Xn. A. mRNA expression of NLRP3, ASC, and caspase 1 detected using qPCR. Protein expression of NLRP3, ASC, caspase-1, pro-caspase-1, IL-1β, and pro-IL-1β detected using western blotting (B) and quantification results (C). *P < 0.05, **P < 0.01, ***P < 0.001 and ****P < 0.0001.
Human Reactive Inflammasome Antibody Sampler Kit Ii, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/human reactive inflammasome antibody sampler kit ii/product/Cell Signaling Technology Inc
Average 85 stars, based on 1 article reviews
human reactive inflammasome antibody sampler kit ii - by Bioz Stars, 2026-04
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Macrophages are myeloid cells of the innate immune system that are found in all human tissues in the body and exhibit anatomical and functional diversity These heterogenous cells are derived from monocyte precursors in the
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Programmed cell death PCD plays important roles in organismal development and immune responses There are three major PCD pathways apoptosis pyroptosis and necroptosis Apoptosis is a non inflammatory cell death and is characterized by a
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MT1H induces p53-dependent autophagy via regulating the key genes in nutrient transportation. (A) Semi-qPCR to verify the downregulated or upregulated genes by MT1H in AGS cells. AGS-tetO-MT1H cells were treated with Dox (2 µg/ml) to induce the expression of ectopic MT1H. 24 h later, cells were harvested for total RNA extraction and reverse transcription followed by semi-qPCR. (B) The cells expressing tetO-MT1H were treated with Dox (2 µg/ml) to induce the expression of ectopic MT1H. 24 h later, cells were harvested for immunoblot analysis with indicated antibodies. NE-PER Nuclear and Cytoplasmic Extraction kit (Thermo) was used to fractionate cells into cytosol compartment and nuclear compartment. (C) MT1H biological functions by KEGG analysis. The participation in mineral absorption was predicted by KEGG-Pathway (https://www.genome.jp/kegg/). (D) Illustrative diagram of MT1H biological functions in gastric cells. The information in the diagram is the combination of our current research and KEGG-Pathway.

Journal: Scientific Reports

Article Title: MT1H inhibits the growth of gastric cancer by regulating SLC6A19/TTC39B/ADM2 and activating p53-dependent autophagy

doi: 10.1038/s41598-025-91319-y

Figure Lengend Snippet: MT1H induces p53-dependent autophagy via regulating the key genes in nutrient transportation. (A) Semi-qPCR to verify the downregulated or upregulated genes by MT1H in AGS cells. AGS-tetO-MT1H cells were treated with Dox (2 µg/ml) to induce the expression of ectopic MT1H. 24 h later, cells were harvested for total RNA extraction and reverse transcription followed by semi-qPCR. (B) The cells expressing tetO-MT1H were treated with Dox (2 µg/ml) to induce the expression of ectopic MT1H. 24 h later, cells were harvested for immunoblot analysis with indicated antibodies. NE-PER Nuclear and Cytoplasmic Extraction kit (Thermo) was used to fractionate cells into cytosol compartment and nuclear compartment. (C) MT1H biological functions by KEGG analysis. The participation in mineral absorption was predicted by KEGG-Pathway (https://www.genome.jp/kegg/). (D) Illustrative diagram of MT1H biological functions in gastric cells. The information in the diagram is the combination of our current research and KEGG-Pathway.

Article Snippet: For immunoblotting, LSD1 (2184), NF-κB p65 (8242T), RelB (4922T), Erk1/2 (9102), p-Erk1/2 (Thr202/Tyr204) (C4370S), and the Human Reactive Cell Death and Autophagy Antibody Sampler Kit (42867) were purchased from Cell Signaling Technology.

Techniques: Expressing, RNA Extraction, Reverse Transcription, Western Blot, Extraction

Fig. 5. Inhibition of PA-NLRP3 inflammasome axis-induced inflammation and ECM degradation by Xn. A. mRNA expression of NLRP3, ASC, and caspase 1 detected using qPCR. Protein expression of NLRP3, ASC, caspase-1, pro-caspase-1, IL-1β, and pro-IL-1β detected using western blotting (B) and quantification results (C). *P < 0.05, **P < 0.01, ***P < 0.001 and ****P < 0.0001.

Journal: Heliyon

Article Title: Xanthohumol alleviates palmitate-induced inflammation and prevents osteoarthritis progression by attenuating mitochondria dysfunction/NLRP3 inflammasome axis.

doi: 10.1016/j.heliyon.2023.e21282

Figure Lengend Snippet: Fig. 5. Inhibition of PA-NLRP3 inflammasome axis-induced inflammation and ECM degradation by Xn. A. mRNA expression of NLRP3, ASC, and caspase 1 detected using qPCR. Protein expression of NLRP3, ASC, caspase-1, pro-caspase-1, IL-1β, and pro-IL-1β detected using western blotting (B) and quantification results (C). *P < 0.05, **P < 0.01, ***P < 0.001 and ****P < 0.0001.

Article Snippet: ADAMTS5 (1:500) was purchased from ABclonal, and collagen II (1:500) was purchased from ThermoFisher Scientific; Human Reactive Inflammasome Antibody Sampler Kit II, p-IκBα (1:1000), IκBα (1:1000), p65 (1:1000), p-p65 (1:1000), anti-rabbit IgG, HRP-linked Antibody (1:1000), anti-mouse IgG, and HRP-linked Antibody (1:1000) were purchased from Cell Signaling Technology.

Techniques: Inhibition, Expressing, Western Blot