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Fucoidan

Fucoidan

产品编号 T7544   CAS 9072-19-9
别名: 岩藻多糖

Fucoidan 是一种 α-淀粉酶和 α-葡萄糖苷酶的有效抑制剂,是一种生物特性多糖。 它具有抗凝血,抗肿瘤,抗氧化和抗脂肪特性。

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Fucoidan Chemical Structure
Fucoidan, CAS 9072-19-9
规格 价格/CNY 货期 数量
100 mg ¥ 133 现货
500 mg ¥ 286 现货
千万补贴 助力科研
BCA蛋白浓度测定试剂盒限时半价
重组蛋白限时优惠
产品目录号及名称: Fucoidan (T7544)
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天然产物信息
生物活性
化学信息
存储 & 溶解度
参考文献
结构类型
产品描述 Fucoidan is found in various species of brown seaweed and algae,with anticancer, antiviral, neuroprotective, immune-modulating.
体外活性 Fucoidan significantly decreased viable cell number in a dose-response manner with an IC50 of 550 ±4.3 μg/mL.?Cell morphology was altered and significant apoptosis was induced when cells were exposed to 550 μg/mL fucoidan for 48 h[1].
体内活性 Intraperitoneal injection of fucoidan in breast cancer models reduced the tumor volume and weight.?The enhanced antitumor efficacy was associated with decreased angiogenesis and increased induction of apoptosis[2].
细胞实验 The influence of fucoidan on B16 melanoma cells and cellular tyrosinase:Cell viability was examined by the cell counting kit-8 assay. Cellular tyrosinase activity and melanin content were determined using spectrophotometric methods and protein expression was analyzed by immunoblotting. Morphological changes in B16 melanoma cells were examined by phase contrast microscopy and apoptosis was analyzed by flow cytometry[1].
动物实验 In vivo, therapy experiments were conducted on Babl/c mice bearing breast cancer.?The tumor volume and weight were measured.?The number of apoptotic cells and microvascular density (MVD) in tumor tissues were assessed by TUNEL and CD34 immunostaining.?Immunohistochemical assays and ELISA assay were used to detect the expression of VEGF in tissues[2].
别名 岩藻多糖
分子量 N/A
CAS No. 9072-19-9

存储

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度

H2O: 10 mM

DMSO: Insoluble

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TargetMol Library Books参考文献

1. Wang Z J , Xu W , Liang J W , et al. EFFECT OF FUCOIDAN ON B16 MURINE MELANOMA CELL MELANIN FORMATION AND APOPTOSI[J]. African Journal of Traditional, Complementary and Alternative Medicines, 2017, 14(4):149-155. 2. Xue M , Ge Y , Zhang J , et al. Anticancer Properties and Mechanisms of Fucoidan on Mouse Breast Cancer In Vitro and In Vivo[J]. PLOS ONE, 2012, 7.

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请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法: 比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL,一共给药动物10 只,您使用的配方为5% DMSO+30% PEG300+5% Tween 80+60% ddH2O。那么您的工作液浓度为2 mg/mL。

母液配置方法:2 mg 药物溶于 50 μL DMSO (母液浓度为 40 mg/mL), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。

体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。

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您可能有的问题的答案可以在抑制剂处理说明中找到,包括如何准备库存溶液,如何存储产品,以及基于细胞的分析和动物实验需要特别注意的问题。

Keywords

Fucoidan 9072-19-9 Others polysaccharide anticoagulant diabetes inhibit Glucosidase antisteatotic 岩藻多糖 Inhibitor α-amylase α-glucosidase. Antioxidant Type 2 anticancer inhibitor

 

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