| Biotarget | 荷兰生产 | Fluorescent DiI Liposomes荧光素DiI脂质体 | C270605 | 5 mL | 2周 | 3550.00 | 2850.00 |
| Biotarget | 荷兰生产 | Fluorescent DiI Liposomes荧光素DiI脂质体 | C270609 | 10 mL | 2周 | 5750.00 | 4650.00 |
荧光对照脂质体将亲脂性染料 DiI 整合于脂质双分子层中。荧光空白脂质体是一类经荧光染料标记的脂质体,便于观测与示踪。在药物递送研究中,这类脂质体可用于探究药物在生物体内的分布、靶向性及释放过程。凭借荧光特性,能够对脂质体进行实时追踪与成像,助力解析药物递送体系的作用效果与作用机制。此外,该产品还可应用于荧光显微镜、生物成像等相关实验场景。
• 粉红色混悬即用型液体
• 适用多种给药途径
• 支持实时追踪与成像
• 荷兰生产,原装进口
| 品牌 | 产地 | 品名 | 货号 | 规格 | 库存 | 目录价 | 促销价 |
| Biotarget | 荷兰生产 | Fluorescent DiI Liposomes荧光素DiI脂质体 | C270605 | 5 mL | 2周 | 3550.00 | 2850.00 |
| Biotarget | 荷兰生产 | Fluorescent DiI Liposomes荧光素DiI脂质体 | C270609 | 10 mL | 2周 | 5750.00 | 4650.00 |
荧光素Dil脂质体(Fluorescent Dil Liposomes)是用来在实验动物体内(invivo)或者体外(invitro)示踪(trace)单核巨噬细胞和神经元等细胞的即用型液体试剂,其也是氯膦酸二钠脂质体(Clodronate Liposomes)的荧光类对照脂质体。 本款荧光对照脂质体将亲脂性染料 DiI整合于脂质双分子层中。其理化性质与 Cell-Del®Clodronate Liposomes氯膦酸盐脂质体产品基本一致,内部未包封活性药物,可借助共聚焦显微镜、流式细胞术(FACS)等常规手段,用于示踪细胞对脂质体的摄取过程。
脂质体(Liposomes)是一种人工膜,由磷脂和胆固醇构成。一般直径在25nm-1um之间。细胞体外(invitro)吞噬实验显示,随着脂质体(Liposome)的直径从100nm到1um,细胞吞噬的脂质体(Liposomes)随之增多,直至高达2um;动物体内(invivo)实验显示,随着直径增大,体内吞噬的脂质体(Liposomes)更多。脂质体(Liposomes)和巨噬细胞(Macrophages)间有最小的间隙,辅以改变脂质体(Liposomes)表面的电荷,尤其是负电荷,能更好促进巨噬细胞对脂质体的吞噬。采用多室的脂质体结构,让包裹更多的药物,从而到达效应的阈浓度。
Dil即DilC18(3),全称为1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate,属于二烷基羰基氰化物类化合物,一种亲脂性花青染料,像其它家族成员(DiO,DiD,DiR和DiA)一样,是最常用的细胞膜荧光探针之一。Dil通过侧向扩散,亲脂性使得整个细胞的细胞膜被染色。 在结合进膜之前,只发出微弱荧光,仅当进入到细胞膜后才可以被激发出很强的荧光。Dil被激发后可以发出橘-红色荧光的荧光,光谱类似于四甲基罗丹明(tetramethylrhodamine,TRITC),通常用作神经元和其它细胞的长期示踪剂。
外观:粉红色混悬液体
脂质组分:磷脂酰胆碱、胆固醇
平均粒径:0.5~3.5 微米
包封染料:Dil。1,1'- 双十八烷基 - 3,3,3',3'- 四甲基吲哚碳花菁高氯酸盐(CAS 号:41085-99-8)
包封药物:Clodronate,水合氯膦酸钠(CAS 号:22560-50-5),浓度 5 mg/mL
缓冲体系:磷酸盐缓冲液
pH 值:7.0~7.5
保质期:未开启瓶体,2~8 ℃条件下可保质 6 个月
储存条件:避光、4 ℃保存,严禁冷冻
运输方式:采用保温包装 + 蓝冰运输
激发波长 / 发射波长:550 nm / 570 nm
注意事项:
• 产品禁止冻存,避免低于0 ℃。
• 产品静置于冰箱中会出现分层现象(瓶底产生沉淀,上层为澄清液)。
• 使用前请轻柔摇晃,直至体系混合均匀,操作过程中避免产生气泡。
• 产品禁止分装。
• 产品避免接触破环脂质体结构的有机试剂和离子去垢剂。
• 荧光素脂质体严格避光
1. van Rooijen N, van Nieuwmegen R. Elimination of phagocytic cells in the spleen after intravenous injection of liposome-encapsulated dichloromethylene diphosphonate. An enzyme-histochemical study. Cell Tissue Res. 1984;238(2):355-8. doi: 10.1007/BF00217308. PMID: 6239690. PubMed ![]()
2. van Rooijen N, van Nieuwmegen R, Kamperdijk EW. Elimination of phagocytic cells in the spleen after intravenous injection of liposome-encapsulated dichloromethylene diphosphonate. Ultrastructural aspects of elimination of marginal zone macrophages. Virchows Arch B Cell Pathol Incl Mol Pathol. 1985;49(4):375-83. doi: 10.1007/BF02912114. PMID: 2867636. PubMed ![]()
3. Claassen E, Kors N, van Rooijen N. Immunomodulation with liposomes: the immune response elicited by liposomes with entrapped dichloromethylene-diphosphonate and surface-associated antigen or hapten. Immunology. 1987 Apr;60(4):509-15. PMID: 2953668; PMCID: PMC1453280. PubMed ![]()
4. van Rooijen N, Kors N, ter Hart H, Claassen E. In vitro and in vivo elimination of macrophage tumor cells using liposome-encapsulated dichloromethylene diphosphonate. Virchows Arch B Cell Pathol Incl Mol Pathol. 1988;54(4):241-5. doi: 10.1007/BF02899217. PMID: 2895535. PubMed ![]()
5. van Rooijen N, Kors N, Kraal G. Characterization of cell populations, reappearing in the mouse spleen after elimination by liposome encapsulated dichloromethylene diphosphonate: reappearance of marginal zone lymphocytes is independent of marginal zone macrophages. Adv Exp Med Biol. 1988;237:889-93. doi: 10.1007/978-1-4684-5535-9_133. PMID: 2978212. PubMed ![]()
6. van Rooijen N, Kors N, Kraal G. Macrophage subset repopulation in the spleen: differential kinetics after liposome-mediated elimination. J Leukoc Biol. 1989 Feb;45(2):97-104. doi: 10.1002/jlb.45.2.97. PMID: 2521666. PubMed ![]()
7. Su D, Van Rooijen N. The role of macrophages in the immunoadjuvant action of liposomes: effects of elimination of splenic macrophages on the immune response against intravenously injected liposome-associated albumin antigen. Immunology. 1989 Mar;66(3):466-70. PMID: 2703258; PMCID: PMC1385238. PubMed ![]()
8. Thepen T, Van Rooijen N, Kraal G. Alveolar macrophage elimination in vivo is associated with an increase in pulmonary immune response in mice. J Exp Med. 1989 Aug 1;170(2):499-509. doi: 10.1084/jem.170.2.499. PMID: 2526847; PMCID: PMC2189410. PubMed ![]()