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    [KO驗證抗體] Rabbit Anti-SIRT1 antibody (bs-0921R)
    ~~~促銷,代碼SSY221101~~~
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    產品編號 bs-0921R
    英文名稱 [KO驗證抗體] SIRT1
    中文名稱 沉默調節蛋白1抗體
    別    名 SIR2L1; NAD-dependent protein deacetylase sirtuin-1; EC:2.3.1.286; hSIRT1; NAD-dependent protein deacylase sirtuin-1; Regulatory protein SIR2 homolog 1; SIR2-like protein 1 (hSIR2); SirtT1 75 kDa fragment; SIR1_HUMAN;   
    Specific References  (17)     |     bs-0921R has been referenced in 17 publications.
    [IF=2.639] Biqi Han. et al. Harmful Effects of Inorganic Mercury Exposure on Kidney Cells: Mitochondrial Dynamics Disorder and Excessive Oxidative Stress. 2021 May 31  WB ;  Human.  
    [IF=5.81] Lin B. et al. Antioxidant Effects of Sophora davidi (Franch.) Skeels on d-Galactose-Induced Aging Model in Mice via Activating the SIRT1/p53 Pathway.. Front Pharmacol. 2021 Dec;12:754554-754554  IHC ;  Mouse.  
    [IF=4.411] Hyo Won Jung. et al. Anticancer Effects of Ursi Fel Extract and Its Active Compound, Ursodeoxycholic Acid, in FRO Anaplastic Thyroid Cancer Cells. Molecules. 2021 Jan;26(17):5309  WB ;  human.  
    [IF=3.998] Haichao Lin. et al. HMGR overexpression and interference affect the expression of steroidogenic genes and cholesterol content in bovine intramuscular adipocytes. Sci Rep-Uk. 2020 Oct;10(1):1-8  WB ;  Cattle.  
    [IF=3.212] Xu Sun. et al. FGF21 Enhances Therapeutic Efficacy and Reduces Side Effects of Dexamethasone in Treatment of Rheumatoid Arthritis. Inflammation. 2021 Feb;44(1):249-260  WB ;  Mouse.  
    [IF=2.634] Shi Lina. et al. Sirt1 Regulates Oxidative Stress in Oxygen-Glucose Deprived Hippocampal Neurons. Front Pediatr. 2020 Aug;8:455  WB ;  Rat.  
    [IF=7.518] Qi Guo. et al. Adiponectin treatment improves insulin resistance in mice by regulating the expression of the mitochondrial-derived peptide MOTS-c and its response to exercise via APPL1–SIRT1–PGC-1α. Diabetologia. 2020 Dec;63(12):2675-2688  WB ;  Mouse.  
    [IF=3.166] Shi et al. Vam3, a derivative of resveratrol, attenuates cigarette smoke-induced autophagy. (2012) Acta.Pharmacol.Si. 33:888-96  IHC-P ;  Mouse.  
    [IF=3.1] Yan, Dongying, et al. "Effects of Aluminium on long‐term Memory in Rats and on SIRT1 Mediating the Transcription of CREB‐Dependent Gene in Hippocampus." Basic & Clinical Pharmacology & Toxicology (2017).  WB ;  Rat.  
    [IF=5.36] Mohan, Mahesh, et al. "Dysregulated miR34a SIRT1 Acetyl p65 Axis Is a Potential Mediator of Immune Activation in the Colon during Chronic Simian Immunodeficiency Virus Infection of Rhesus Macaques." The Journal of Immunology (2014): 1401447.  
    [IF=2] Da HU. et al. Nicotinic Acid against Acetaminophen-Induced Hepatotoxicity via Sirt1/Nrf2 Antioxidative Pathway in Mice. J Nutr Sci Vitaminol. 2021 Jun;67(3):145-152  WB ;  Mouse.  
    [IF=4.545] Kai Kanget al. FGF21 attenuates neurodegeneration through modulating neuroinflammation and oxidant-stress. Biomed Pharmacother . 2020 Sep;129:110439.  WB ;  mouse.  
    [IF=4.486] Ming Qiet al. Postnatal growth retardation is associated with intestinal mucosa mitochondrial dysfunction and aberrant energy status in piglets. J Cell Mol Med . 2020 Sep;24(17):10100-10111.  WB ;  pig.  
    [IF=2.575] Chen H et al. Sevoflurane attenuates cognitive dysfunction and NLRP3-dependent caspase-1/11-GSDMD pathway-mediated pyroptosis in the hippocampus via upregulation of SIRT1 in a sepsis model. Arch Physiol Biochem. 2020 Jun 13;1-8.  WB ;  Mouse.  
    [IF=1.692] Gao D et al. Protective effect of astaxanthin against contrast-induced acute kidney injury via SIRT1-p53 pathway in rats.(2018)Int Urol Nephrol  WB ;  Rat.  
    [IF=1.69] Zeng et al. Hypothermic machine perfusion ameliorates inflammation during ischemia?reperfusion injury via sirtuin?1?mediated deacetylation of nuclear factor?κB p65 in rat livers donated after circulatory death. (2017) Mol.Med.Rep. 16:8649-8656  WB ;  Rat.  
    [IF=3.74] Hu, Zheng, et al. "5-Aminolevulinic acid-mediated sonodynamic therapy induces anti-tumor effects in malignant melanoma via p53-miR-34a-Sirt1 axis." Journal of dermatological science 79.2 (2015): 155-162.  WB ;  Mouse.  
    研究領域 細胞生物  免疫學  染色質和核信號  微生物學  新陳代謝  表觀遺傳學  
    抗體來源 Rabbit
    克隆類型 Polyclonal
    交叉反應 Human, Mouse,  (predicted: Rat, Chicken, Cow, Horse, Rabbit, )
    產品應用 WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 Flow-Cyt=1μg/Test IF=1:100-500 (石蠟切片需做抗原修復)
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    理論分子量 58/81kDa
    細胞定位 細胞核 細胞漿 
    性    狀 Liquid
    濃    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human SirtT1: 101-200/747 
    亞    型 IgG
    純化方法 affinity purified by Protein A
    緩 沖 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
    保存條件 Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
    注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    PubMed PubMed
    產品介紹 This gene encodes a member of the sirtuin family of proteins, homologs to the yeast Sir2 protein. Members of the sirtuin family are characterized by a sirtuin core domain and grouped into four classes. The functions of human sirtuins have not yet been determined; however, yeast sirtuin proteins are known to regulate epigenetic gene silencing and suppress recombination of rDNA. Studies suggest that the human sirtuins may function as intracellular regulatory proteins with mono-ADP-ribosyltransferase activity. The protein encoded by this gene is included in class I of the sirtuin family. Alternative splicing results in multiple transcript variants.

    Function:
    NAD-dependent protein deacetylase, which regulates processes such as apoptosis and muscle differentiation by deacetylating key proteins. Deacetylates 'Lys-382' of p53/TP53 and impairs its ability to induce proapoptotic program and modulate cell senescence. Deacetylates TAF1B and thereby represses rDNA transcription by the RNA polymerase I. Deacetylates 'Lys-266' of SUV39H1, leading to its activation. Deacetylates 'Lys-26' of HIST1H1E. Involved in HES1- and HEY2-mediated transcriptional repression. Inhibits skeletal muscle differentiation by deacetylating PCAF and MYOD1. May serve as a sensor of the cytosolic ratio of NAD(+)/NADH, which is essential in skeletal muscle cell differentiation. Deacetylates 'Lys-16' of histone H4 (in vitro). Component of the eNoSC (energy-dependent nucleolar silencing) complex, a complex that mediates silencing of rDNA in response to intracellular energy status and acts by recruiting histone-modifying enzymes. The eNoSC complex is able to sense the energy status of cell: upon glucose starvation, elevation of NAD(+)/NADP(+) ratio activates SIRT1, leading to histone H3 deacetylation followed by dimethylation of H3 at 'Lys-9' (H3K9me2) by SUV39H1 and the formation of silent chromatin in the rDNA locus. Deacetylates H2A. In case of HIV-1 infection, interacts with and deacetylates the viral Tat protein. Deacetylates APEX1 at 'Lys-6' and 'Lys-7'. Stimulates cellular AP endonuclease activity by promoting the association of APEX1 to XRCC1.

    Subunit:
    Found in a complex with PCAF and MYOD1. Component of the eNoSC complex, composed of SIRT1, SUV39H1 and RRP8. Interacts with HES1, HEY2 and PML. Interacts with RPS19BP1/AROS. Interacts with KIAA1967/DBC1 (via N-terminus); the interaction disrupts the interaction between SIRT1 and p53/TP53. Interacts with SETD7; the interaction induces the dissociation of SIRT1 from p53/TP53 and increases p53/TP53 activity. Interacts with MYCN, NR1I2, CREBZF, TSC2, TLE1, FOS, JUN, NR0B2, PPARG, NCOR, IRS1, IRS2 and NMNAT1. Interacts with HNF1A; the interaction occurs under nutrient restriction. Interacts with SUZ12; the interaction mediates the association with the PRC4 histone methylation complex which is specific as an association with PCR2 and PCR3 complex variants is not found. Interacts with HIV-1 tat.

    Subcellular Location:
    Nucleus, PML body. Cytoplasm. Note=Recruited to the nuclear bodies via its interaction with PML. Colocalized with APEX1 in the nucleus. May be found in nucleolus, nuclear euchromatin, heterochromatin and inner membrane. Shuttles between nucleus and cytoplasm.
    SirtT1 75 kDa fragment: Cytoplasm. Mitochondrion.

    Tissue Specificity:
    Widely expressed.

    Post-translational modifications:
    Methylated on multiple lysine residues; methylation is enhanced after DNA damage and is dispensable for deacetylase activity toward p53/TP53.
    Phosphorylated. Phosphorylated by STK4/MST1, resulting in inhibition of SIRT1-mediated p53/TP53 deacetylation. Phosphorylation by MAPK8/JNK1 at Ser-27, Ser-47, and Thr-530 leads to increased nuclear localization and enzymatic activity.
    Phosphorylation at Thr-530 by DYRK1A and DYRK3 activates deacetylase activity and promotes cell survival. Phosphorylation by mammalian target of rapamycin complex 1 (mTORC1) at Ser-47 inhibits deacetylation activity. Phosphorylated by CaMK2, leading to increased p53/TP53 and NF-kappa-B p65/RELA deacetylation activity (By similarity). Phosphorylation at Ser-27 implicating MAPK9 is linked to protein stability. There is some ambiguity for some phosphosites: Ser-159/Ser-162 and Thr-544/Ser-545. Proteolytically cleaved by cathepsin B upon TNF-alpha treatment to yield catalytic inactive but stable SirtT1 75 kDa fragment (75SirT1).
    S-nitrosylated by GAPDH, leading to inhibit the NAD-dependent protein deacetylase activity.

    Similarity:
    Belongs to the sirtuin family.
    Contains 1 deacetylase sirtuin-type domain.

    SWISS:
    Q96EB6

    Gene ID:
    23411

    Database links:

    Entrez Gene: 23411 Human

    Entrez Gene: 93759 Mouse

    Entrez Gene: 309757 Rat

    Omim: 604479 Human

    SwissProt: Q96EB6 Human

    SwissProt: Q923E4 Mouse

    Unigene: 369779 Human

    Unigene: 351459 Mouse



    在Sirtuin蛋白家族中,sirtuin 1(沉默信息調節子)參與多種新陳代謝活動,包括DNA的自我保護和修復,抑制脂質過氧化積累,抑制其他細胞凋亡相關基因的表達以及和細胞壽命相關的活動。限制攝入的熱量可以加強SIRT1的表達,從而延長了壽命。
    SIRT蛋白成為多種生物過程的調節者也參與衰老的調控。在研究最多的SIRT蛋白中,SIRT1與各種非組蛋白或者轉錄因子相互作用,包括p53、FOXO蛋白、p300、NFkB和MyoD,sirtuins可參與凋亡、細胞存活、轉錄和代謝等過程。以sirtuins為靶標的藥物可能在治療衰老、癌癥、糖尿病和神經退行性變中有用。
    產品圖片
    Sample: Lane 1: Hela (Human) Cell Lysate at 30 ug Lane 2: NIH/3T3 (Mouse) Cell Lysate at 30 ug Lane 3: HepG2 (Human) Cell Lysate at 30 ug Lane 4: 293T (Human) Cell Lysate at 30 ug Lane 5: Testis (Mouse) Lysate at 40 ug Primary: Anti-SIRT1 (bs-0921R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 116/95 kD Observed band size: 116 kD
    Sample:
    Hela(Human) Cell Lysate at 30 ug
    Hela KO SIRT1 (Human) Cell Lysate at 30 ug
    Primary: Anti- SIRT1 (bs-0921R) at 1/500 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 58/81 kD
    Observed band size: 75/150 kD
    Paraformaldehyde-fixed, paraffin embedded (human glioma tissue); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (SIRT1) Polyclonal Antibody, Unconjugated (bs-0921R) at 1:200 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
    Paraformaldehyde-fixed, paraffin embedded (mouse brain); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (SIRT1) Polyclonal Antibody, Unconjugated (bs-0921R) at 1:200 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
    Tissue/cell: human endometrium carcinoma; 4% Paraformaldehyde-fixed and paraffin-embedded;
    Antigen retrieval: citrate buffer ( 0.01M, pH 6.0 ), Boiling bathing for 15min; Block endogenous peroxidase by 3% Hydrogen peroxide for 30min; Blocking buffer (normal goat serum,C-0005) at 37℃ for 20 min;
    Incubation: Anti-SIRT1 Polyclonal Antibody, Unconjugated(bs-0921R) 1:200, overnight at 4°C, followed by conjugation to the secondary antibody(SP-0023) and DAB(C-0010) staining
    Blank control (blue line): MCF 7 (blue).
    Primary Antibody (green line): Rabbit Anti-SIRT1 antibody (bs-0921R)
    Dilution: 3μg /10^5 cells;
    Isotype Control Antibody (orange line): Rabbit IgG .
    Secondary Antibody (white blue line): Goat anti-rabbit IgG-FITC
    Dilution: 1μg /test.
    Protocol
    The cells were fixed with 70% methanol (Overnight at 4℃) and then permeabilized with 90% ice-cold methanol for 30 min on ice. Cells stained with Primary Antibody for 30 min at room temperature. The cells were then incubated in 1 X PBS/2%BSA/10% goat serum to block non-specific protein-protein interactions followed by the antibody for 15 min at room temperature. The secondary antibody used for 40 min at room temperature. Acquisition of 20,000 events was performed.
    Blank control:HL-60.
    Primary Antibody (green line): Rabbit Anti-SIRT1 antibody (bs-2257R)
    Dilution: 1μg /10^6 cells;
    Isotype Control Antibody (orange line): Rabbit IgG .
    Secondary Antibody : Goat anti-rabbit IgG-AF488
    Dilution: 1μg /test.
    Protocol
    The cells were fixed with 4% PFA (10min at room temperature)and then permeabilized with 0.1% PBST for 20 min at room temperature. The cells were then incubated in 5%BSA to block non-specific protein-protein interactions for 30 min at room temperature .Cells stained with Primary Antibody for 30 min at room temperature. The secondary antibody used for 40 min at room temperature. Acquisition of 20,000 events was performed.
    Blank control:HL-60.
    Primary Antibody (green line): Rabbit Anti-SIRT1 antibody (bs-0921R)
    Dilution: 1μg /10^6 cells;
    Isotype Control Antibody (orange line): Rabbit IgG .
    Secondary Antibody : Goat anti-rabbit IgG-AF488
    Dilution: 1μg /test.
    Protocol
    The cells were fixed with 4% PFA (10min at room temperature)and then permeabilized with 0.1% PBST for 20 min at room temperature. The cells were then incubated in 5%BSA to block non-specific protein-protein interactions for 30 min at room temperature .Cells stained with Primary Antibody for 30 min at room temperature. The secondary antibody used for 40 min at room temperature. Acquisition of 20,000 events was performed.
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