SIRT1 Polyclonal antibody (13161-1-AP)
EC:2.3.1.-; EC:2.3.1.286; hSIR2; hSIRT1; NAD-dependent protein deacetylase sirtuin-1
用户验证的应用
经验证应用
| 项目 | 详情 |
|---|---|
| Positive WB detected in | HEK-293 cells, HeLa cells, MDA-MB-231 cells |
| Positive IP detected in | HeLa cells |
| Positive IHC detected in | human colon cancer tissue, human lung cancer tissue, mouse testis tissue Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0 |
| Positive IF/ICC detected in | HepG2 cells, HeLa cells |
推荐稀释说明
It is recommended that this reagent should be titrated in each testing system to obtain optimal results. Sample-dependent, Check data in validation data gallery.
详细信息
背景信息
SIRT1, also named SIR2L1, contains a deacetylase sirtuin-type domain and belongs to the sirtuin family. The post-translation modified SIRT1 is a 110-130 kDa protein, which contains one deacetylase sirtuin-type domain.After phosphorylation modification, this target protein may present double bands ranging from 110 to 120 kDa. The 75-80 kDa SirT1 fragment was detected to lack the carboxy-terminus (PMID:21305533). SirT1 exists a 57-61 kDa isoform. SIRT1 may be found in nucleolus, nuclear euchromatin, heterochromatin, and inner membrane. It can shuttle between the nucleus and cytoplasm. SIRT1 regulates processes such as apoptosis and muscle differentiation by deacetylating key proteins. SIRT1 in particular initiates several signaling events relevant to cardioprotection, including activation of endothelial nitric oxide synthase, INS receptor signaling, and autophagy. In addition, SIRT1 activation elicits resistance to oxidative stress via the regulation of transcription factors and co-activators such as FOXO, Hif-2a, and NF-kB. SIRT1 regulates the p53-dependent DNA damage response pathway by binding to and deacetylating p53, specifically at Lysine 382. This antibody is a rabbit polyclonal antibody raised against residues near the N terminus of human SIRT1.
文献引用 (125)
Dual-responsive nanoparticles targeting ACE-II senescence for therapeutic mitigation of acute lung injury.
靶向ACE-II衰老的双重响应纳米颗粒用于治疗性缓解急性肺损伤
Mesoporous Prussian blue nanoparticle neuroconduit for the biological therapy targeting oxidative stress reduction, inflammation inhibition, and nerve regeneration
介孔普鲁士蓝纳米粒子神经导管用于针对氧化应激减少、炎症抑制和神经再生的生物治疗
Aptamer-Conjugated Exosomes Ameliorate Diabetes-Induced Muscle Atrophy by Enhancing SIRT1/FoxO1/3a-Mediated Mitochondrial Function
适体偶联外泌体通过增强SIRT1/FoxO1/3a介导的线粒体功能来改善糖尿病引起的肌肉萎缩
TACC3 enhances glycolysis in bladder cancer cells through inducing acetylation of c-Myc
TACC3通过诱导c-Myc乙酰化增强膀胱癌细胞的糖酵解作用
Apoptotic vesicles derived from bone marrow mesenchymal stem cells increase angiogenesis in a hind limb ischemia model via the NAMPT/SIRT1/FOXO1 axis
骨髓间充质干细胞来源的凋亡囊泡通过 NAMPT/SIRT1/FOXO1 轴增加后肢缺血模型中的血管生成
Nicotinamide mononucleotide promotes female germline stem cell proliferation by activating the H4K16ac-Hmgb1-Fyn-PLD signaling pathway through epigenetic remodeling.
烟酰胺单核苷酸通过表观遗传重塑激活 H4K16ac-Hmgb1-Fyn-PLD 信号通路,促进雌性生殖细胞增殖
Time Does Matter: The Cellular Response to Resveratrol Varies Depending on the Exposure Duration.
时间很重要:细胞对白藜芦醇的反应会因接触时间的长短而有所不同
Cardiac protection of wogonin in mice with pulmonary fibrosis by regulating Sirt1/ γ-H2AX pathway.
黄芩苷通过调节 Sirt1/ α-H2AX 通路对肺纤维化小鼠发挥心脏保护作用
New insights into ovarian regression-related mitochondrial dysfunction in the late-laying period.
对产蛋后期卵巢退化相关线粒体功能障碍的新见解
Exogenous H(2)S reduces oxidative stress induced by lipid mixture in HepG2 cells through USP22/SIRT1 axis.
外源性 H(2)S 通过 USP22/SIRT1 轴降低 HepG2 细胞中脂质混合物引起的氧化应激
- 1
- 2
- 3
- 4
- 5
- 6
- 13