Peroxidase
CAS No. 9003-99-0
Peroxidase ( —— )
产品货号. M27103 CAS No. 9003-99-0
过氧化物酶来自辣根。过氧化物酶积极参与氧化活性氧、先天免疫、激素生物合成和多种疾病的发病机制。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥243 | 有现货 |
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| 5MG | ¥348 | 有现货 |
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| 10MG | ¥284 | 有现货 |
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| 25MG | ¥462 | 有现货 |
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| 50MG | ¥672 | 有现货 |
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| 100MG | ¥988 | 有现货 |
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| 200MG | ¥1604 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Peroxidase
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述过氧化物酶来自辣根。过氧化物酶积极参与氧化活性氧、先天免疫、激素生物合成和多种疾病的发病机制。
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产品描述Peroxidase comes from horseradish. Peroxidase actively involves in oxidizing reactive oxygen species, innate immunity, hormone biosynthesis and pathogenesis of several diseases.(In Vitro):Peroxidases exist as monomers, dimmers or tetramers and their gene locations also vary among different chromosomes. Peroxidases have some organ, tissue, cellular and sub-cellular specific distribution patterns, performing some specific functions. Peroxidases belong to a large family of isoenzymes present in almost all living organisms. These are generally heme containing enzymes ranging in Mw from 35-100 Kd. Mammalian peroxidases are much larger proteins (576-738 amino acids) than the plant counterparts.
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体外实验Peroxidases belong to a large family of isoenzymes present in almost all living organisms. These are generally heme containing enzymes ranging in Mw from 35-100 Kd. Mammalian peroxidases are much larger proteins (576-738 amino acids) than the plant counterparts. Peroxidases exist as monomers, dimmers or tetramers and their gene locations also vary among different chromosomes. Peroxidases have some organ, tissue, cellular and sub-cellular specific distribution patterns, performing some specific functions.
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体内实验——
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同义词——
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通路Others
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靶点Other Targets
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受体Aldose Reductase| COX-2
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研究领域——
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适应症——
化学信息
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CAS Number9003-99-0
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分子量——
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分子式——
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纯度>98% (HPLC)
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溶解度In Vitro:?H2O : 33.33 mg/mL
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SMILES——
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Zheng X, et al. The molecular basis for inhibition of sulindac and its metabolites towards human aldose reductase. FEBS Lett. 2012 Jan 2;586(1):55-9.
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