
DAPI染色液
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- 保存条件:
-20℃,避光,有效期12个月
- 保质期:
12个月
- 英文名:
-
- 库存:
现货
- 供应商:
爱必信(上海)生物科技有限公司
- CAS号:
-
- 规格:
10mL/50mL
| 规格: | 10mL | 产品价格: | ¥138.0 |
|---|---|---|---|
| 规格: | 50mL | 产品价格: | ¥480.0 |
| 描述 | DAPI染色液(DAPI Staining Solution)是适用于常见细胞和组织细胞核染色的染色液。DAPI,即2-(4-Amidinophenyl)-6-indolecarbamidine dihydrochloride,也称DAPI dihydrochloride,分子式为C16H15N5·2HCl ,分子量为350.25,是可以穿透细胞膜的蓝色荧光染料,和双链DNA结合后可以产生比DAPI自身强20多倍的荧光,灵敏度高于EB。 DAPI染色常用于细胞凋亡检测,染色后用荧光显微镜观察或流式细胞仪检测。DAPI也常用于普通的细胞核染色以及某些特定情况下的双链DNA染色。DAPI的激发波长为340nm,发射波长为488nm,DAPI和双链DNA结合后,激发波长为364nm,发射波长为454nm。 |
| 浓度 | 3μM |
| 使用方法 | DAPI染色实验流程: 1、贴壁细胞的复染: 1.1样品准备: 使用恰当的固定剂固定样品。一般情况下,最后用 DAPI 对细胞进行染色。 1.2复染流程: (1)用 PBS 短暂平衡样品; (2)加入适量的 DAPI 染液,保证所有细胞均被覆盖,孵育 3~5min; (3)用 PBS 漂洗样品数次,用吸水纸将多余的液体吸干; (4)用配有恰当滤片的荧光显微镜观察样品。 2、悬浮细胞的复染: 2.1 样品准备: (1)收集悬浮细胞 2×105 ~1×106 个细胞,通过离心,使细胞沉淀,弃上清; (2)轻弹试管,使沉淀在剩余的液体中重悬,在加入 1mL PBS; (3)将细胞悬液缓慢的加入 4mL 乙醇中,同时以最大的速度涡旋。将含有细胞的乙醇在 -20℃放置5~15min; (4)通过离心,使细胞沉淀,弃上清; (5)轻弹试管,使沉淀松散,在加入 5ml PBS。 2.2 复染流程: (1)离心使细胞沉淀,弃上清,轻弹试管,使沉淀松散,加入 2~3mL DAPI 染液; (2)室温下孵育 15min; (3)如果使用荧光显微镜观察细胞,将样品离心后,弃上清,用新鲜的缓冲液重悬沉淀。 在显微镜载片上滴加一滴细胞悬液,加盖片后观察。 |
| 储存/保存方法 | -20℃,避光,有效期12个月。 |
| 注意事项 | 1、荧光染料都存在淬灭的问题,建议染色后尽快检测; 2、避免反复冻融,否则容易失效; 3、DAPI对人体有刺激性,请注意适当防护; 4、为了您的安全和健康,请穿实验服并戴一次性手套操作。 |
| 别名 | DAPI Staining Solution |
| 外观 | 二甲基甲酰胺溶液 |
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DAPI 染色 1.原理DAPI为4’,6二脒基-2-苯吲哚(4’,6―diamidino-2―phenylindole)能与双链DNA小槽,特别是AT碱基结合,也可插入少于3个连续AT碱基对的DNA序列中。当它与双链DNA结合时,荧光强度增强20倍,而与单链DNA结合则无荧光增强现象,因此是一种简易、快速和敏感地检测DNA的方法。DAPI的荧光强度虽较Hoechst低,但荧光稳定性优于Hoechst;其特异性较溴化乙啶(ethidlium bromide,EB)和碘
DAPI Staining To visualize DNA, incubate fixed samples with 100 ng/ml 4',6'-diamidino-2-phenylindole hydrochloride (DAPI) in PBS for 30 min. Rinse 3x with PBTw. Materials PBS: Sambrook et al. (Molecular Cloning ). PBTw
DAPI Counterstaining Protocols
实验试剂 Choose one of the following forms of DAPI: DAPI dihydrochloride (MW = 350.3) DAPI dihydrochloride, FluoroPure™ grade (=98% pure) DAPI dilactate (MW = 457.5) For fluorescence microscopy











