DAPI溶液(1mg/ml)
产品名称: DAPI溶液(1mg/ml)
英文名称: DAPI solution,1mg/ml
产品编号: C0060
产品价格: 0
产品产地: 北京
品牌商标: solarbio
更新时间: 2023-08-11T10:26:26
使用范围: null
- 联系人 : 索莱宝-龚思雨
- 地址 : 北京市通州区中关村科技园区通州园金桥科技产业基地景盛南四街15号85A三层
- 邮编 : 101102
- 所在区域 : 北京
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供应DAPI溶液(1mg/ml)
保存:-20℃,有效期至少 2 年
产品说明:
DAPI(4’,6-二脒基-2-苯基吲哚二盐酸盐)是一种能够与 DNA 中大部分 A,T 碱基相互结合的荧光染料o常用于荧光显微镜观测。因为 DAPI 可以透过完整的细胞膜o它可以用于活细胞和固定细胞的染色。当 DAPI 与双链 DNA 结合时, 大吸收波长为 358nm, 大发射波长为 461nm。DAPI 的发射光为蓝色,DAPI 和绿色荧光蛋白 GFP 或 Texas Red 染剂(红色荧光染剂)的发射波长仅有少部分重叠,可以利用这项特性在单一的样品上进行多重荧光染色。
本产品为 DAPI 水溶液,纯度≥90%,浓度为 1mg/ml。使用时根据实验不同直接将本产品用相应溶液稀释到工作浓度。
使用方法: (仅供参考)
对于培养细胞
1, 取适量 DAPI 水溶液加到 PBS 中,制备成 5-15 μg/ml 的 DAPI 溶液。
2, 将 1/10 培养基体积的 DAPI 溶液加入到细胞培养基中。
3, 在 37℃培养细胞 10-20 分钟。
4, 用 PBS 或合适的缓冲液洗细胞两次。
5, 置于荧光显微镜下观察,激发波长 360-400nm。
对于组织切片
制好的玻片上滴加几滴稀释的 DAPI 染液,染色 10 分钟,流水冲去染液,滤纸吸除多余水分,加一滴荧光封片液,置于荧光显微镜下观察。
注意事项:
DAPI 被普遍认为具有致癌性,操作时应戴手套,并避免交叉污染。
本产品需避光,并尽量避免反复冻融。
相关产品:
C0080 碘化丙锭 PI溶液(1mg/ml)
CA1020 ANNEXIN V-FITC/PI凋亡检测试剂盒
12100 DMEM(H)培养基
S9000 特级胎牛血清
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图片为DAPI固体,溶液试剂以实物为准。本产品由索莱宝实验室自己配制,以下为相关试剂
货号 | 试剂名称 | 包装规格 | 价格 |
R8070 | 剥离硅烷 | 200ml | 160 |
B8150 | 亲和硅烷 | 25ml | 200 |
C0020 | Hoechst 33258染色液(即用型) | 10ml/50ml | 120/320 |
C0030 | Hoechst 33342染色液(即用型) | 10ml/50ml | 120/320 |
C0040 | 台盼蓝染色液(0.4%) | 50ml/100 | 120/200 |
C0060 | DAPI溶液(1mg/ml) | 1ml/1ml*10 | 200/1200 |
C0065 | DAPI溶液(即用型) | 10ml/50ml | 120/320 |
C0080 | 碘化丙锭PI溶液(1mg/ml) | 1ml/1ml*10 | 80/500 |
C1010 | 柠檬酸钠缓冲液0.01mol/L, pH6.0,干粉 | 1L/2L | 8/12 |
C1013 | 柠檬酸钠缓冲液0.1mol/L, pH4.5,无菌溶液 | 100/500ml | 50/160 |
C1031 | 柠檬酸钠抗原修复液(1×) | 100/500ml | 50/160 |
C1032 | 柠檬酸钠抗原修复液(50×) | 100/500ml | 70/220 |
C1033 | EDTA抗原修复液(1×) | 100/500ml | 50/160 |
C1034 | EDTA抗原修复液(50×) | 100/500ml | 70/220 |
C1035 | 冰冻切片抗原修复液(1×) | 100/500ml | 100/320 |
C1036 | 细胞爬片抗原修复液(1×) | 100/500ml | 100/320 |
C1050 | ELISA包被液(1x) | 100/500ml | 70/200 |
C1055 | ELISA包被液(10x) | 100/500ml | 100/300 |
C1058 | ELISA终止液 | 100/500ml | 70/200 |
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