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gamma secretase inhibitor ix dapt  (Selleck Chemicals)


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    Structured Review

    Selleck Chemicals gamma secretase inhibitor ix dapt
    Gamma Secretase Inhibitor Ix Dapt, supplied by Selleck Chemicals, used in various techniques. Bioz Stars score: 96/100, based on 375 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/%CE%B3+secretase+inhibitor+dapt/DAPT/pm41751772-237-35-40
    Average 96 stars, based on 375 article reviews
    gamma secretase inhibitor ix dapt - by Bioz Stars, 2026-11
    96/100 stars

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    Related Articles

    Transfection:

    Article Title: NCAM2 promotes targeting of APP from the cell surface to BACE1-containing recycling endosomes.
    Article Snippet: .. Human iPSC-derived neurons were transfected with NCAM2 siRNA or control siRNA at differentiation day 19 and maintained for 48 h. Cells were treated with 10 μM γ-secretase inhibitor DAPT (Selleckchem, Cat. #S2215) for 24 h, washed twice with ice-cold PBS, treated with ice-cold lysis buffer (1 % sodium deoxycholate, 1 % Triton X-100, 50 mM Tris-Cl, 150 mM NaCl, 1 mM EDTA, 1 mM PMSF and cOmplete protease inhibitor (Roche), pH 7.4), scraped off and incubated for 30 min on ice. ..

    Control:

    Article Title: NCAM2 promotes targeting of APP from the cell surface to BACE1-containing recycling endosomes.
    Article Snippet: .. Human iPSC-derived neurons were transfected with NCAM2 siRNA or control siRNA at differentiation day 19 and maintained for 48 h. Cells were treated with 10 μM γ-secretase inhibitor DAPT (Selleckchem, Cat. #S2215) for 24 h, washed twice with ice-cold PBS, treated with ice-cold lysis buffer (1 % sodium deoxycholate, 1 % Triton X-100, 50 mM Tris-Cl, 150 mM NaCl, 1 mM EDTA, 1 mM PMSF and cOmplete protease inhibitor (Roche), pH 7.4), scraped off and incubated for 30 min on ice. ..

    Lysis:

    Article Title: NCAM2 promotes targeting of APP from the cell surface to BACE1-containing recycling endosomes.
    Article Snippet: .. Human iPSC-derived neurons were transfected with NCAM2 siRNA or control siRNA at differentiation day 19 and maintained for 48 h. Cells were treated with 10 μM γ-secretase inhibitor DAPT (Selleckchem, Cat. #S2215) for 24 h, washed twice with ice-cold PBS, treated with ice-cold lysis buffer (1 % sodium deoxycholate, 1 % Triton X-100, 50 mM Tris-Cl, 150 mM NaCl, 1 mM EDTA, 1 mM PMSF and cOmplete protease inhibitor (Roche), pH 7.4), scraped off and incubated for 30 min on ice. ..

    Protease Inhibitor:

    Article Title: NCAM2 promotes targeting of APP from the cell surface to BACE1-containing recycling endosomes.
    Article Snippet: .. Human iPSC-derived neurons were transfected with NCAM2 siRNA or control siRNA at differentiation day 19 and maintained for 48 h. Cells were treated with 10 μM γ-secretase inhibitor DAPT (Selleckchem, Cat. #S2215) for 24 h, washed twice with ice-cold PBS, treated with ice-cold lysis buffer (1 % sodium deoxycholate, 1 % Triton X-100, 50 mM Tris-Cl, 150 mM NaCl, 1 mM EDTA, 1 mM PMSF and cOmplete protease inhibitor (Roche), pH 7.4), scraped off and incubated for 30 min on ice. ..

    Incubation:

    Article Title: NCAM2 promotes targeting of APP from the cell surface to BACE1-containing recycling endosomes.
    Article Snippet: .. Human iPSC-derived neurons were transfected with NCAM2 siRNA or control siRNA at differentiation day 19 and maintained for 48 h. Cells were treated with 10 μM γ-secretase inhibitor DAPT (Selleckchem, Cat. #S2215) for 24 h, washed twice with ice-cold PBS, treated with ice-cold lysis buffer (1 % sodium deoxycholate, 1 % Triton X-100, 50 mM Tris-Cl, 150 mM NaCl, 1 mM EDTA, 1 mM PMSF and cOmplete protease inhibitor (Roche), pH 7.4), scraped off and incubated for 30 min on ice. ..

    Blocking Assay:

    Article Title: Spatiotemporal dynamics of early oogenesis in pigs
    Article Snippet: .. To block the NOTCH signaling pathway and ECM protein production during in vitro culture, 100 μM γ-secretase inhibitor DAPT (Selleck, S2215) and 20 nM matrix metalloproteinase inhibitor doxycycline (Selleck, S5159) were supplemented to the culture media as previously reported [ , ]. .. All quantification plots were presented as mean ± SEM, and a two-tailed, unpaired t -test was used for comparing groups of two using GraphPad Prism (version 5.01).

    Article Title: Notch activation downregulates EZH2 to thereby attenuate endothelial cell proliferation and angiogenesis via MYC destabilization.
    Article Snippet: Aims: Angiogenesis, a tightly regulated process involving dynamic endothelial cell (EC) proliferation, is critical in both physiological and pathological contexts such as ocular neovascular disorders.. While Notch signaling is known to regulate angiogenesis, its downstream molecular mechanisms remain incompletely understood.. Main methods: Gene-modified mice with a Cdh5-CreERT transgene were generated to block Notch signaling in ECs.

    In Vitro:

    Article Title: Spatiotemporal dynamics of early oogenesis in pigs
    Article Snippet: .. To block the NOTCH signaling pathway and ECM protein production during in vitro culture, 100 μM γ-secretase inhibitor DAPT (Selleck, S2215) and 20 nM matrix metalloproteinase inhibitor doxycycline (Selleck, S5159) were supplemented to the culture media as previously reported [ , ]. .. All quantification plots were presented as mean ± SEM, and a two-tailed, unpaired t -test was used for comparing groups of two using GraphPad Prism (version 5.01).

    other:

    Article Title: Cadmium exposure impaired the uterine decidualization through inducing the imbalance of mitochondrial fusion and fission.
    Article Snippet: Cadmium (Cd), a widespread environmental pollutant, has toxic effects on spermatogenesis and sperm motility, but its role in uterine decidualization remains unknown.. This study revealed that Cd exposure during early pregnancy might impair the uterine decidualization along with the disordered proliferation and apoptosis of stromal cells, resulting in the reduction of mouse neonatal number and birth weight.. After disrupting the binding of Ca2+ and LNR-C, Cd exposure ligand-independently activated the NOTCH1 signaling and then restrained the expression of nuclear TAZ via RBPJ-targeting LATS.

    Article Title: Nicotinamide mononucleotide ameliorates hypertriglyceridemia pancreatitis via NAD + /SIRT1-mediated TXNIP suppression and NOTCH pathway for accelerated repair-associated processes.
    Article Snippet: Background & Aims: Acute pancreatitis (AP) is a life-threatening condition, and hypertriglyceridemia (HTG) is recognized as a factor exacerbating AP and impeding pancreatic regeneration.. Nicotinamide mononucleotide (NMN), a precursor in the biosynthesis of nicotinamide adenine dinucleotide (NAD), is extensively utilized to restore NAD levels.. However, the impact of NMN on HTG-AP has not been previously addressed, which prompted our investigation into its effects and underlying mechanisms in this study.

    Concentration Assay:

    Article Title: Notch activation downregulates EZH2 to thereby attenuate endothelial cell proliferation and angiogenesis via MYC destabilization.
    Article Snippet: Aims: Angiogenesis, a tightly regulated process involving dynamic endothelial cell (EC) proliferation, is critical in both physiological and pathological contexts such as ocular neovascular disorders.. While Notch signaling is known to regulate angiogenesis, its downstream molecular mechanisms remain incompletely understood.. Main methods: Gene-modified mice with a Cdh5-CreERT transgene were generated to block Notch signaling in ECs.

    Recombinant:

    Article Title: Melatonin promotes the proliferation and differentiation of antler chondrocytes via RUNX2 dependent on the interaction between NOTCH1 and SHH signaling pathways.
    Article Snippet: Funding information Natural Science Foundation of Jilin Province, Grant/Award Number: 20220101287JC; National Natural Science Foundation of China, Grant/Award Number: 31873003 Abstract Melatonin (MT), an endogenous hormone secreted by pineal gland, has the sedative, anti‐inflammatory and antioxidant functions.. However, there are few studies on whether MT affects the proliferation and differentiation of antler chondrocytes.. The present study investigated the influences of MT on the proliferation and differentiation of antler chondrocytes, explored its regulation on runt‐related transcription factor 2 (RUNX2), NOTCH1 and sonic hedgehog (SHH) signaling, and elucidated their interplays.



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    miR-223-3p suppresses SIRT1 transcription via the Notch1/Hes1 signaling pathway, thereby promoting microglial lactylation and M1 polarization. (A) RT-qPCR analysis of Notch1 and Hes1 mRNA levels. (B) Western blot analysis of NICD1 and Hes1 protein expression. (C) Western blot analysis of SIRT1 expression following silencing Hes1. (D) Western blot detection of global lactylation levels. (E) RT-qPCR analysis of microglial polarization markers. (F and G) RT-qPCR and western blot detection of SIRT1 following treatment with Notch1 inhibitor <t>DAPT</t> (20 nM; 24 h). (H) Western blot detection of global lactylation levels. (I) RT-qPCR analysis of microglial polarization markers. (J) Western blot analysis of iNOS and Arg-1 protein expression. (K) Flow cytometric analysis of ROS levels. * P<0.05, ** P<0.01 and *** P<0.001. miR, microRNA; SIRT1, sirtuin 1; RT-qPCR, reverse transcription-quantitative PCR; iNOS, inducible nitric oxide synthase; ROS, reactive oxygen species; NC, negative control; ns, not significant.
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    Image Search Results


    miR-223-3p suppresses SIRT1 transcription via the Notch1/Hes1 signaling pathway, thereby promoting microglial lactylation and M1 polarization. (A) RT-qPCR analysis of Notch1 and Hes1 mRNA levels. (B) Western blot analysis of NICD1 and Hes1 protein expression. (C) Western blot analysis of SIRT1 expression following silencing Hes1. (D) Western blot detection of global lactylation levels. (E) RT-qPCR analysis of microglial polarization markers. (F and G) RT-qPCR and western blot detection of SIRT1 following treatment with Notch1 inhibitor DAPT (20 nM; 24 h). (H) Western blot detection of global lactylation levels. (I) RT-qPCR analysis of microglial polarization markers. (J) Western blot analysis of iNOS and Arg-1 protein expression. (K) Flow cytometric analysis of ROS levels. * P<0.05, ** P<0.01 and *** P<0.001. miR, microRNA; SIRT1, sirtuin 1; RT-qPCR, reverse transcription-quantitative PCR; iNOS, inducible nitric oxide synthase; ROS, reactive oxygen species; NC, negative control; ns, not significant.

    Journal: International Journal of Molecular Medicine

    Article Title: miR-223-3p promotes microglial lactylation and M1 polarization via the FBXW7/Notch1/Hes1/SIRT1 axis

    doi: 10.3892/ijmm.2026.5849

    Figure Lengend Snippet: miR-223-3p suppresses SIRT1 transcription via the Notch1/Hes1 signaling pathway, thereby promoting microglial lactylation and M1 polarization. (A) RT-qPCR analysis of Notch1 and Hes1 mRNA levels. (B) Western blot analysis of NICD1 and Hes1 protein expression. (C) Western blot analysis of SIRT1 expression following silencing Hes1. (D) Western blot detection of global lactylation levels. (E) RT-qPCR analysis of microglial polarization markers. (F and G) RT-qPCR and western blot detection of SIRT1 following treatment with Notch1 inhibitor DAPT (20 nM; 24 h). (H) Western blot detection of global lactylation levels. (I) RT-qPCR analysis of microglial polarization markers. (J) Western blot analysis of iNOS and Arg-1 protein expression. (K) Flow cytometric analysis of ROS levels. * P<0.05, ** P<0.01 and *** P<0.001. miR, microRNA; SIRT1, sirtuin 1; RT-qPCR, reverse transcription-quantitative PCR; iNOS, inducible nitric oxide synthase; ROS, reactive oxygen species; NC, negative control; ns, not significant.

    Article Snippet: The SIRT1 inhibitor EX527 (10 μ M; 49843-98-3; TargetMol) and the SIRT1 activator SRT1720 (5 μ M; 1001645-58-4; TargetMol) were added separately and incubated for 24 h. The γ-secretase inhibitor DAPT (20 nM; cat. no. HY-13027; MedChemExpress) was administered in parallel experiments, while DMSO served as the vehicle control.

    Techniques: Quantitative RT-PCR, Western Blot, Expressing, Reverse Transcription, Real-time Polymerase Chain Reaction, Negative Control