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anti sirt 3 antibody  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc anti sirt 3 antibody
    Anti Sirt 3 Antibody, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/sirt/pm41683751-175-18-20
    Average 86 stars, based on 1 article reviews
    anti sirt 3 antibody - by Bioz Stars, 2026-09
    86/100 stars

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    Related Articles

    other:


    Article Title: High-Intensity Interval Training Remodels the Proteome and Acetylome of Human Skeletal Muscle
    Article Snippet: MFN2: #11925, Cell Signaling 772 Technologies, 80 kDa; MYLK2: PA5-29324, Invitrogen, 65 kDa; NAMPT: A300-779A, Bethyl 773 Laboratories, 56 kDa; OXPHOS antibody cocktail: ab110411, Abcam, 15-55 kDa; SIRT-1: 07-131, 774 Millipore, 80 kDa; SIRT-3: #5490, Cell Signaling Technologies, 28 kDa; SIRT-5: #8782, Cell 775 Signaling Technologies, 30 kDa; HRP conjugated goat anti-rabbit (4010-05, SouthernBiotech) and a 776 goat anti-mouse (P0447, DAKO Denmark) were used as secondary antibodies.

    Western Blot:

    Article Title: Telomerase therapy reverses vascular senescence and extends lifespan in progeria mice.
    Article Snippet: The lysates were then used in BCA protein assay kit (Thermo Fisher, No. 23225) to measure total protein. .. The total protein amounts of 8–12lg per sample were used for running into the premade (Bio-Rad) gel running at 100 V for 1 h. Proteins were then transferred to nitrocellulose membranes with Bio-Rad transfer system (Trans-Blot Turbo) and blocked in 1 Quant Clean Western buffer (cat No. R2001) for 1 h. The blots were then incubated with dilute primary antibody in 5% BSA, 1 TBS, 0.1% Tween-20 at 4 C with gentle shaking, overnight (SIRT1: Cell Signaling 2028S, 1:1000; telomerase: NOVUS NB110-89471, 1:2000; progerin: Millipore 05-1231, 1:500; GAPDH: Cell Signaling D16H11, 1:2000). ..

    Incubation:

    Article Title: Telomerase therapy reverses vascular senescence and extends lifespan in progeria mice.
    Article Snippet: The lysates were then used in BCA protein assay kit (Thermo Fisher, No. 23225) to measure total protein. .. The total protein amounts of 8–12lg per sample were used for running into the premade (Bio-Rad) gel running at 100 V for 1 h. Proteins were then transferred to nitrocellulose membranes with Bio-Rad transfer system (Trans-Blot Turbo) and blocked in 1 Quant Clean Western buffer (cat No. R2001) for 1 h. The blots were then incubated with dilute primary antibody in 5% BSA, 1 TBS, 0.1% Tween-20 at 4 C with gentle shaking, overnight (SIRT1: Cell Signaling 2028S, 1:1000; telomerase: NOVUS NB110-89471, 1:2000; progerin: Millipore 05-1231, 1:500; GAPDH: Cell Signaling D16H11, 1:2000). ..

    Gentle:

    Article Title: Telomerase therapy reverses vascular senescence and extends lifespan in progeria mice.
    Article Snippet: The lysates were then used in BCA protein assay kit (Thermo Fisher, No. 23225) to measure total protein. .. The total protein amounts of 8–12lg per sample were used for running into the premade (Bio-Rad) gel running at 100 V for 1 h. Proteins were then transferred to nitrocellulose membranes with Bio-Rad transfer system (Trans-Blot Turbo) and blocked in 1 Quant Clean Western buffer (cat No. R2001) for 1 h. The blots were then incubated with dilute primary antibody in 5% BSA, 1 TBS, 0.1% Tween-20 at 4 C with gentle shaking, overnight (SIRT1: Cell Signaling 2028S, 1:1000; telomerase: NOVUS NB110-89471, 1:2000; progerin: Millipore 05-1231, 1:500; GAPDH: Cell Signaling D16H11, 1:2000). ..



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    The regulation of H3K18ac by BRD3 degradation is mediated by HDACs, and CCL5 is its target (A) The expression of several deacetylase enzymes (HDAC1, HDAC2, Sirt1, and Sirt3) in control group, LPS group, and D072 treatment group experiments in vitro . (B) The expression levels of SIRT1 under various treatments (LPS stimulation, D072 treatment, or siBRD3 knockdown), Sirt1 changes in proteins and mRNA. (C) The mRNA levels of cxcl10, ccl5, HK3, and nos2 in control group, LPS group, D072 treatment group, D072 + SIRT1 inhibitor (EX-527 treated) group in vitro . (D) The expression levels of CCL5, CXCL10, HK3, and NO2 under the intervention of each group of HDAC inhibitors. (Inhibitor terminology and function: SB: sodium butanoate [HDACs inhibitor], EX-527 <t>[SIRT1</t> <t>inhibitor],</t> <t>SIRT-IN-2</t> [SIRT1, 2, 3 inhibitors], SIRT6-IN-5 [SIRT6 inhibitor], and 97491 [SIRT7 inhibitor]). (E) The expression changes of H3K18ac under the intervention of each group of HDAC inhibitors. (Inhibitor terminology and function: SB: sodium butanoate [HDACs inhibitor], EX-527 [SIRT1 inhibitor], SIRT-IN-2 [SIRT1, 2, 3 inhibitors], SIRT6-IN-5 [SIRT6 inhibitor], and 97491 [SIRT7 inhibitor]). (A) Upper: representative western blot images of HDAC1, HDAC2, SIRT1, and SIRT3 in each group. Lower: quantification of the relative changes of the left ( n = 3/group; mean ± SD; ns, p > 0.05, ∗p < 0.05, ∗∗∗p < 0.001; one-way ANOVA). (B) Left: representative western blot images and the corresponding quantification of the relative protein levels of SIRT1 in each group. Right: quantification of the relative mRNA changes of the SIRT1 in different groups. ( n = 3/group; mean ± SD; ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001; one-way ANOVA). (C) Quantification of the mRNA level of Cxcl10 , Ccl5 , Hk3 , and inos after SIRT1 inhibitor EX-527 treatment. ( n = 3/group; mean ± SD; ∗∗p < 0.01, ∗∗∗p < 0.001; one-way ANOVA). (D) Quantification of the mRNA level of Cxcl10 , Ccl5 , Hk3 , and inos under different HDAC inhibitor treatment. ( n = 3/group; mean ± SD; ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001; one-way ANOVA). Inhibitor terminology and function: SB: sodium butanoate (HDACs inhibitor), EX-527 (SIRT1 inhibitor), SIRT-IN-2 (SIRT1, 2, 3 inhibitors), SIRT6-IN-5 (SIRT6 inhibitor), and 97491 (SIRT7 inhibitor). (E) Quantification of the relative H3K18ac protein level under each treatment. ( n = 3/group; mean ± SD; ∗∗∗p < 0.001; one-way ANOVA). (F) Left: transwell images of different groups; scale bars: 100 μm. Right: quantification of migration cells under each treatment. ( n = 3/group; mean ± SD; ∗∗∗p < 0.001; one-way ANOVA). (G) Quantification statistics concentration of CCL5 in each group. ( n = 3/group; mean ± SD; ∗∗∗p < 0.001; one-way ANOVA).
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    The regulation of H3K18ac by BRD3 degradation is mediated by HDACs, and CCL5 is its target (A) The expression of several deacetylase enzymes (HDAC1, HDAC2, Sirt1, and Sirt3) in control group, LPS group, and D072 treatment group experiments in vitro . (B) The expression levels of SIRT1 under various treatments (LPS stimulation, D072 treatment, or siBRD3 knockdown), Sirt1 changes in proteins and mRNA. (C) The mRNA levels of cxcl10, ccl5, HK3, and nos2 in control group, LPS group, D072 treatment group, D072 + SIRT1 inhibitor (EX-527 treated) group in vitro . (D) The expression levels of CCL5, CXCL10, HK3, and NO2 under the intervention of each group of HDAC inhibitors. (Inhibitor terminology and function: SB: sodium butanoate [HDACs inhibitor], EX-527 <t>[SIRT1</t> <t>inhibitor],</t> <t>SIRT-IN-2</t> [SIRT1, 2, 3 inhibitors], SIRT6-IN-5 [SIRT6 inhibitor], and 97491 [SIRT7 inhibitor]). (E) The expression changes of H3K18ac under the intervention of each group of HDAC inhibitors. (Inhibitor terminology and function: SB: sodium butanoate [HDACs inhibitor], EX-527 [SIRT1 inhibitor], SIRT-IN-2 [SIRT1, 2, 3 inhibitors], SIRT6-IN-5 [SIRT6 inhibitor], and 97491 [SIRT7 inhibitor]). (A) Upper: representative western blot images of HDAC1, HDAC2, SIRT1, and SIRT3 in each group. Lower: quantification of the relative changes of the left ( n = 3/group; mean ± SD; ns, p > 0.05, ∗p < 0.05, ∗∗∗p < 0.001; one-way ANOVA). (B) Left: representative western blot images and the corresponding quantification of the relative protein levels of SIRT1 in each group. Right: quantification of the relative mRNA changes of the SIRT1 in different groups. ( n = 3/group; mean ± SD; ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001; one-way ANOVA). (C) Quantification of the mRNA level of Cxcl10 , Ccl5 , Hk3 , and inos after SIRT1 inhibitor EX-527 treatment. ( n = 3/group; mean ± SD; ∗∗p < 0.01, ∗∗∗p < 0.001; one-way ANOVA). (D) Quantification of the mRNA level of Cxcl10 , Ccl5 , Hk3 , and inos under different HDAC inhibitor treatment. ( n = 3/group; mean ± SD; ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001; one-way ANOVA). Inhibitor terminology and function: SB: sodium butanoate (HDACs inhibitor), EX-527 (SIRT1 inhibitor), SIRT-IN-2 (SIRT1, 2, 3 inhibitors), SIRT6-IN-5 (SIRT6 inhibitor), and 97491 (SIRT7 inhibitor). (E) Quantification of the relative H3K18ac protein level under each treatment. ( n = 3/group; mean ± SD; ∗∗∗p < 0.001; one-way ANOVA). (F) Left: transwell images of different groups; scale bars: 100 μm. Right: quantification of migration cells under each treatment. ( n = 3/group; mean ± SD; ∗∗∗p < 0.001; one-way ANOVA). (G) Quantification statistics concentration of CCL5 in each group. ( n = 3/group; mean ± SD; ∗∗∗p < 0.001; one-way ANOVA).
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    86
    Servicebio Inc sirt 1
    The regulation of H3K18ac by BRD3 degradation is mediated by HDACs, and CCL5 is its target (A) The expression of several deacetylase enzymes (HDAC1, HDAC2, Sirt1, and Sirt3) in control group, LPS group, and D072 treatment group experiments in vitro . (B) The expression levels of SIRT1 under various treatments (LPS stimulation, D072 treatment, or siBRD3 knockdown), Sirt1 changes in proteins and mRNA. (C) The mRNA levels of cxcl10, ccl5, HK3, and nos2 in control group, LPS group, D072 treatment group, D072 + SIRT1 inhibitor (EX-527 treated) group in vitro . (D) The expression levels of CCL5, CXCL10, HK3, and NO2 under the intervention of each group of HDAC inhibitors. (Inhibitor terminology and function: SB: sodium butanoate [HDACs inhibitor], EX-527 <t>[SIRT1</t> <t>inhibitor],</t> <t>SIRT-IN-2</t> [SIRT1, 2, 3 inhibitors], SIRT6-IN-5 [SIRT6 inhibitor], and 97491 [SIRT7 inhibitor]). (E) The expression changes of H3K18ac under the intervention of each group of HDAC inhibitors. (Inhibitor terminology and function: SB: sodium butanoate [HDACs inhibitor], EX-527 [SIRT1 inhibitor], SIRT-IN-2 [SIRT1, 2, 3 inhibitors], SIRT6-IN-5 [SIRT6 inhibitor], and 97491 [SIRT7 inhibitor]). (A) Upper: representative western blot images of HDAC1, HDAC2, SIRT1, and SIRT3 in each group. Lower: quantification of the relative changes of the left ( n = 3/group; mean ± SD; ns, p > 0.05, ∗p < 0.05, ∗∗∗p < 0.001; one-way ANOVA). (B) Left: representative western blot images and the corresponding quantification of the relative protein levels of SIRT1 in each group. Right: quantification of the relative mRNA changes of the SIRT1 in different groups. ( n = 3/group; mean ± SD; ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001; one-way ANOVA). (C) Quantification of the mRNA level of Cxcl10 , Ccl5 , Hk3 , and inos after SIRT1 inhibitor EX-527 treatment. ( n = 3/group; mean ± SD; ∗∗p < 0.01, ∗∗∗p < 0.001; one-way ANOVA). (D) Quantification of the mRNA level of Cxcl10 , Ccl5 , Hk3 , and inos under different HDAC inhibitor treatment. ( n = 3/group; mean ± SD; ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001; one-way ANOVA). Inhibitor terminology and function: SB: sodium butanoate (HDACs inhibitor), EX-527 (SIRT1 inhibitor), SIRT-IN-2 (SIRT1, 2, 3 inhibitors), SIRT6-IN-5 (SIRT6 inhibitor), and 97491 (SIRT7 inhibitor). (E) Quantification of the relative H3K18ac protein level under each treatment. ( n = 3/group; mean ± SD; ∗∗∗p < 0.001; one-way ANOVA). (F) Left: transwell images of different groups; scale bars: 100 μm. Right: quantification of migration cells under each treatment. ( n = 3/group; mean ± SD; ∗∗∗p < 0.001; one-way ANOVA). (G) Quantification statistics concentration of CCL5 in each group. ( n = 3/group; mean ± SD; ∗∗∗p < 0.001; one-way ANOVA).
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    ROC Curve Analysis for HO-1, Nrf-2 and SIRT-1. HO-1 (cut-off value 0.87, sensitivity 78.3%, specificity 76.7%); Nrf-2 (cut-off value 9.8 sensitivity 70%, specificity 73.3%); SIRT-1 (cut-off value 8.3, sensitivity 75%, specificity 70%). Abbreviations: HO-1: heme oxygenases-1; Nrf-2: nuclear factor erythroid 2-related factor 2; SIRT-1: Sirtuin 1

    Journal: Metabolic Brain Disease

    Article Title: The SIRT-1/Nrf-2/HO-1 antioxidant defense axis in adult attention-deficit/hyperactivity disorder

    doi: 10.1007/s11011-026-01845-5

    Figure Lengend Snippet: ROC Curve Analysis for HO-1, Nrf-2 and SIRT-1. HO-1 (cut-off value 0.87, sensitivity 78.3%, specificity 76.7%); Nrf-2 (cut-off value 9.8 sensitivity 70%, specificity 73.3%); SIRT-1 (cut-off value 8.3, sensitivity 75%, specificity 70%). Abbreviations: HO-1: heme oxygenases-1; Nrf-2: nuclear factor erythroid 2-related factor 2; SIRT-1: Sirtuin 1

    Article Snippet: Serum HO-1, NRF-2, and SIRT-1 concentrations were analyzed using ELISA kits according to the manufacturers’ standard protocols (BT Lab, Human Heme Oxygenase-1: Cat. No. E0932Hu; BT Lab, Human Nuclear Factor Erythroid 2-Related Factor 2: Cat. No. E3244Hu; BT Lab, Human Sirtuin-1: Cat. No. E2557Hu; Jiaxing Korain Biotech, Jiaxing, China) on a Rel Assay automated ELISA reader (Biobase Biodusty Co., Ltd., Jinan, China).

    Techniques:

    The regulation of H3K18ac by BRD3 degradation is mediated by HDACs, and CCL5 is its target (A) The expression of several deacetylase enzymes (HDAC1, HDAC2, Sirt1, and Sirt3) in control group, LPS group, and D072 treatment group experiments in vitro . (B) The expression levels of SIRT1 under various treatments (LPS stimulation, D072 treatment, or siBRD3 knockdown), Sirt1 changes in proteins and mRNA. (C) The mRNA levels of cxcl10, ccl5, HK3, and nos2 in control group, LPS group, D072 treatment group, D072 + SIRT1 inhibitor (EX-527 treated) group in vitro . (D) The expression levels of CCL5, CXCL10, HK3, and NO2 under the intervention of each group of HDAC inhibitors. (Inhibitor terminology and function: SB: sodium butanoate [HDACs inhibitor], EX-527 [SIRT1 inhibitor], SIRT-IN-2 [SIRT1, 2, 3 inhibitors], SIRT6-IN-5 [SIRT6 inhibitor], and 97491 [SIRT7 inhibitor]). (E) The expression changes of H3K18ac under the intervention of each group of HDAC inhibitors. (Inhibitor terminology and function: SB: sodium butanoate [HDACs inhibitor], EX-527 [SIRT1 inhibitor], SIRT-IN-2 [SIRT1, 2, 3 inhibitors], SIRT6-IN-5 [SIRT6 inhibitor], and 97491 [SIRT7 inhibitor]). (A) Upper: representative western blot images of HDAC1, HDAC2, SIRT1, and SIRT3 in each group. Lower: quantification of the relative changes of the left ( n = 3/group; mean ± SD; ns, p > 0.05, ∗p < 0.05, ∗∗∗p < 0.001; one-way ANOVA). (B) Left: representative western blot images and the corresponding quantification of the relative protein levels of SIRT1 in each group. Right: quantification of the relative mRNA changes of the SIRT1 in different groups. ( n = 3/group; mean ± SD; ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001; one-way ANOVA). (C) Quantification of the mRNA level of Cxcl10 , Ccl5 , Hk3 , and inos after SIRT1 inhibitor EX-527 treatment. ( n = 3/group; mean ± SD; ∗∗p < 0.01, ∗∗∗p < 0.001; one-way ANOVA). (D) Quantification of the mRNA level of Cxcl10 , Ccl5 , Hk3 , and inos under different HDAC inhibitor treatment. ( n = 3/group; mean ± SD; ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001; one-way ANOVA). Inhibitor terminology and function: SB: sodium butanoate (HDACs inhibitor), EX-527 (SIRT1 inhibitor), SIRT-IN-2 (SIRT1, 2, 3 inhibitors), SIRT6-IN-5 (SIRT6 inhibitor), and 97491 (SIRT7 inhibitor). (E) Quantification of the relative H3K18ac protein level under each treatment. ( n = 3/group; mean ± SD; ∗∗∗p < 0.001; one-way ANOVA). (F) Left: transwell images of different groups; scale bars: 100 μm. Right: quantification of migration cells under each treatment. ( n = 3/group; mean ± SD; ∗∗∗p < 0.001; one-way ANOVA). (G) Quantification statistics concentration of CCL5 in each group. ( n = 3/group; mean ± SD; ∗∗∗p < 0.001; one-way ANOVA).

    Journal: iScience

    Article Title: BRD3 PROTAC degrader targets H3K18ac to alleviate retinal microglia-driven uveitis

    doi: 10.1016/j.isci.2025.114526

    Figure Lengend Snippet: The regulation of H3K18ac by BRD3 degradation is mediated by HDACs, and CCL5 is its target (A) The expression of several deacetylase enzymes (HDAC1, HDAC2, Sirt1, and Sirt3) in control group, LPS group, and D072 treatment group experiments in vitro . (B) The expression levels of SIRT1 under various treatments (LPS stimulation, D072 treatment, or siBRD3 knockdown), Sirt1 changes in proteins and mRNA. (C) The mRNA levels of cxcl10, ccl5, HK3, and nos2 in control group, LPS group, D072 treatment group, D072 + SIRT1 inhibitor (EX-527 treated) group in vitro . (D) The expression levels of CCL5, CXCL10, HK3, and NO2 under the intervention of each group of HDAC inhibitors. (Inhibitor terminology and function: SB: sodium butanoate [HDACs inhibitor], EX-527 [SIRT1 inhibitor], SIRT-IN-2 [SIRT1, 2, 3 inhibitors], SIRT6-IN-5 [SIRT6 inhibitor], and 97491 [SIRT7 inhibitor]). (E) The expression changes of H3K18ac under the intervention of each group of HDAC inhibitors. (Inhibitor terminology and function: SB: sodium butanoate [HDACs inhibitor], EX-527 [SIRT1 inhibitor], SIRT-IN-2 [SIRT1, 2, 3 inhibitors], SIRT6-IN-5 [SIRT6 inhibitor], and 97491 [SIRT7 inhibitor]). (A) Upper: representative western blot images of HDAC1, HDAC2, SIRT1, and SIRT3 in each group. Lower: quantification of the relative changes of the left ( n = 3/group; mean ± SD; ns, p > 0.05, ∗p < 0.05, ∗∗∗p < 0.001; one-way ANOVA). (B) Left: representative western blot images and the corresponding quantification of the relative protein levels of SIRT1 in each group. Right: quantification of the relative mRNA changes of the SIRT1 in different groups. ( n = 3/group; mean ± SD; ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001; one-way ANOVA). (C) Quantification of the mRNA level of Cxcl10 , Ccl5 , Hk3 , and inos after SIRT1 inhibitor EX-527 treatment. ( n = 3/group; mean ± SD; ∗∗p < 0.01, ∗∗∗p < 0.001; one-way ANOVA). (D) Quantification of the mRNA level of Cxcl10 , Ccl5 , Hk3 , and inos under different HDAC inhibitor treatment. ( n = 3/group; mean ± SD; ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001; one-way ANOVA). Inhibitor terminology and function: SB: sodium butanoate (HDACs inhibitor), EX-527 (SIRT1 inhibitor), SIRT-IN-2 (SIRT1, 2, 3 inhibitors), SIRT6-IN-5 (SIRT6 inhibitor), and 97491 (SIRT7 inhibitor). (E) Quantification of the relative H3K18ac protein level under each treatment. ( n = 3/group; mean ± SD; ∗∗∗p < 0.001; one-way ANOVA). (F) Left: transwell images of different groups; scale bars: 100 μm. Right: quantification of migration cells under each treatment. ( n = 3/group; mean ± SD; ∗∗∗p < 0.001; one-way ANOVA). (G) Quantification statistics concentration of CCL5 in each group. ( n = 3/group; mean ± SD; ∗∗∗p < 0.001; one-way ANOVA).

    Article Snippet: SIRT-IN-2 , Targetmol , T12929.

    Techniques: Expressing, Histone Deacetylase Assay, Control, In Vitro, Knockdown, Western Blot, Migration, Concentration Assay