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Rabbit Anti-AGEs  antibody (bs-1158R)
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说明书: 50ul  100ul  200ul
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包装/询价

产品编号 bs-1158R
英文名称 AGEs
中文名称 晚期糖基化终末产物抗体
别    名 advanced glycosylation end products; AGE.  
Specific References  (17)     |     bs-1158R has been referenced in 17 publications.
[IF=14.593] Wanyi Zhou. et al. Glucose and MMP-9 dual-responsive hydrogel with temperature sensitive self-adaptive shape and controlled drug release accelerates diabetic wound healing. Bioact Mater. 2022 Jan;:  IF ;  Rat.  
[IF=7.169] Zou Ting-feng. et al. Fisetin treatment alleviates kidney injury in mice with diabetes-exacerbated atherosclerosis through inhibiting CD36/fibrosis pathway. ACTA PHARMACOL SIN. 2023 May;:1-10  IF,WB ;  Mouse.  
[IF=7.129] Juanjuan Duan. et al. Benzo[a]pyrene and a high-fat diet induce aortic injury and promote low-density lipoprotein accumulation in the endothelium. ECOTOX ENVIRON SAFE. 2023 Jul;259:115011  IHC ;  Mouse.  
[IF=6.78] Zhuozhou Hu. et al. Acyclovir alleviates insulin resistance via activating PKM1 in diabetic mice. LIFE SCI. 2022 Sep;304:120725  WB ;  Mouse.  
[IF=6.312] Hee-Weon Lee. et al. Glyoxal-Lysine Dimer, an Advanced Glycation End Product, Induces Oxidative Damage and Inflammatory Response by Interacting with RAGE. Antioxidants-Basel. 2021 Sep;10(9):1486  WB ;  Mouse.  
[IF=6.208] Haiyan Zhou. et al. Glycation of Tie-2 Inhibits Angiopoietin-1 Signaling Activation and Angiopoietin-1-Induced Angiogenesis. INT J MOL SCI. 2022 Jan;23(13):7137  IHC ;  Human.  
[IF=6.147] Dedert Cass. et al. Progranulin Preserves Autophagy Flux and Mitochondrial Function in Rat Cortical Neurons Under High Glucose Stress. FRONT CELL NEUROSCI. 2022 Jul;0:354  WB ;  Rat.  
[IF=5.27] Huang, Kaipeng, et al. "Sirt1 resists AGEs-induced expressions of FN and TGF-β1 by activating the Nrf2/ARE pathway in GMCs." Free Radical Biology and Medicine (2013).  WB ;  Rat.  
[IF=5.151] Kim DY et al. Eucalyptol Inhibits Advanced Glycation End Products‐Induced Disruption of Podocyte Slit Junctions by Suppressing Rage‐Erk‐C‐Myc Signaling Pathway.Mol Nutr Food Res. 2018 Oct;62(19):e1800302.  WB&IHC-P ;  Mouse.  
[IF=4.082] Eun-Jung Leeet al. Coumarin Ameliorates Impaired Bone Turnover by Inhibiting the Formation of Advanced Glycation End Products in Diabetic Osteoblasts and Osteoclasts. Biomolecules . 2020 Jul 15;10(7):1052.  WB ;  mouse.  
[IF=3.75] Andressa S. Sousa. et al. Evaluation of coronary function in female rats with severe type 1 diabetes: Effects of combined treatment with insulin and pyridoxamine. MICROVASC RES. 2022 Dec;:104474  WB ;  Rat.  
[IF=3.571] Oh H et al. Asaronic Acid Attenuates Macrophage Activation toward M1 Phenotype through Inhibition of NF-κB Pathway and JAK-STAT Signaling in Glucose-Loaded Murine Macrophages. J Agric Food Chem. 2019 Aug 26.  WB ;  Mouse.  
[IF=3.352] Wei-Yu Yeh. et al. Functional chicken-liver hydrolysates ameliorate insulin resistance and cognitive decline in streptozotocin-induced diabetic mice. Poultry Sci. 2022 Mar;:101887  WB ;  Mouse.  
[IF=3.21] Tanaka M et al. Effects of combined treatment with blood flow restriction and low intensity electrical stimulation on diabetes mellitus-associated muscle atrophy in rats.J Diabetes. (2018) Sep 18  WB ;  Calf.  
[IF=2.66] Ye, Ruidong, et al. "Ginsenoside Rd attenuates early oxidative damage and sequential inflammatory response after transient focal ischemia in rats." Neurochemistry international 58.3 (2011): 391-398.  WB ;  Rat.  
[IF=1.39] Ryuma Haraguchi et al. New Insights into the Pathogenesis of Diabetic Nephropathy: Proximal Renal Tubules Are Primary Target of Oxidative Stress in Diabetic Kidney. Acta Histochem Cytochem . 2020 Apr 28;53(2):21-31.  IHC ;  mouse.  
[IF=1.11] Lu, Lin, et al. "Effects of atorvastatin on progression of diabetic nephropathy and local RAGE and soluble RAGE expressions in rats." Journal of Zhejiang University SCIENCE B 12.8 (2011): 652-659.  WB ;  Rat.  
研究领域 细胞生物  免疫学  糖尿病  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Rat,Mouse,Human
产品应用 WB=1:500-2000, IHC-P=1:100-500, IHC-F=1:100-500, IF=1:100-500, Flow-Cyt=1ug/Test, ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 62kDa
细胞定位 分泌型蛋白 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 AGEs 
亚    型 IgG
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件 Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
产品介绍 Advanced Glycation End products (AGEs) are the result of a chain of chemical reactions after an initial glycation reaction. The intermediate products are known, variously, as Amadori, Schiff base and Maillard products, named after the researchers who first described them. (The literature is inconsistent in applying these terms. For example, Maillard reaction products are sometimes considered intermediates and sometimes end products.) Side products generated in intermediate steps may be oxidizing agents (such as hydrogen peroxide), or not (such as beta amyloid proteins).[1] "Glycosylation" is sometimes used for "glycation" in the literature, usually as 'non-enzymatic glycosylation. The AGE modified BSA was produced by reacting BSA with glycolaldehyde under sterile conditions followed by extensive dialysis and purification steps.

SWISS:
P02769

Gene ID:
AGEs

AGEs又称非酶糖基化终末产物(AGEs) 是蛋白质、脂质和核酸等大分子的游离氨基与还原性单糖的醛基反应所生成的稳定的共价化合物, 在体内的积累、增多是导致糖尿病等多种疾病及其并发症的关键因素。AGEs的异常增多,可直接或间接地对机体产生致病作用。
晚期糖基化终末产物-AGEs的相关学说
晚期糖基化终末产物(Advanced glycation endproducts,AGEs)是一类经由糖,包括通过Maillard反应形成的代谢中间产物化学修饰的蛋白。AGEs具有高度交联性。 AGE与AGE受体(如RAGE)的相互作用诱导了受体承载细胞核因子-κB(NF—κB)的活化,同时这一作用还诱导了细胞因子、生长因子及黏附分子表达的增加。
在糖尿病方面,晚期糖基化终末产物(AGEs)可引起体内组织一系列病理生理改变,是导致糖尿病慢性并发症的重要致病因素。在健康人群中AGEs也随年龄增加在组织中持续积累,并参与衰老过程。由于糖尿病和衰老均可导致骨代谢紊乱,甚至出现骨质疏松及脱钙。
AGEs具有广泛的致病作用。AGEs形成后引起蛋白质分子间广泛交联,致使蛋白质结构、机械强度、溶解性和配位结合等性质均发生改变。体内多种蛋白质糖基化可从多个方面影响机体,如引起血管通透性增大、血管基底膜增厚和细胞外基质积聚等。AGEs与其细胞表面受体(RAGE)结合,通过趋化和活化单核巨噬细胞,激活转录因子NF-KB,促进细胞因子和组织因子的释放,灭活一氧化氮和产生氧自由基等途径,参与糖尿病慢性并发症的发生和发展 。由于AGEs的不可逆性,即使高血糖被纠正后,AGEs水平也不能回复到正常,而继续在组织中累积。从组织AGEs自然解释出的反应中间物,如不能经肾脏消除,可再次结合到其他结构上,发生AGEs的“第二次”或“第三次”生成,致病作用加重。
产品图片

Sample:
Lane 1: Kidney (Mouse) Tissue Lysate at 40 ug
Lane 2: Lung (Mouse) Tissue Lysate at 40 ug
Lane 3: Large intestine (Mouse) Tissue Lysate at 40 ug
Lane 4: Testis (Rat) Tissue Lysate at 40 ug
Lane 5: Lung (Rat) Tissue Lysate at 40 ug
Lane 6: Large intestine (Rat) Tissue Lysate at 40 ug
Lane 7: U87MG (Human) Cell Lysate at 30 ug
Primary: Anti-AGEs (bs-1158R) at 1/1000 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Observed band size: 62 kD

Tissue/cell: Rat kidney tissue; 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-AGEs Polyclonal Antibody, Unconjugated(bs-1158R) 1:200, overnight at 4°C, followed by conjugation to the secondary antibody(SP-0023) and DAB(C-0010) staining
Tissue/cell: rat kidney tissue; 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-AGEs Polyclonal Antibody, Unconjugated(bs-1158R) 1:200, overnight at 4°C, followed by conjugation to the secondary antibody(SP-0023) and DAB(C-0010) staining
Blank control: MCF7.
Primary Antibody (green line): Rabbit Anti-AGEs antibody (bs-1158R)
Dilution: 1μg /10^6 cells;
Isotype Control Antibody (orange line): Rabbit IgG .
Secondary Antibody : Goat anti-rabbit IgG-AF647
Dilution: 1μg /test.
Protocol
The cells were 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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