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细胞核染料Hoechst 33342 20mM水溶液 CAS 875756-97-1

英文名称:Hoechst 33342 *20 mM solution in water*
产品参数
Ex (nm)352Em (nm)454
分子量561.93溶剂Water
存储条件在零下15度以下保存, 避免光照
产品概述

产品货期

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产品优势  

1.常作为DAPI的替代染色方案

2.DNA特异性结合,实现精准核酸标记

 

适用范围

用于标记活细胞与固定细胞

 

产品介绍

Hoechst荧光染料是一类广泛应用于DNA标记的荧光染色剂家族,在荧光显微镜技术中具有重要作用。作为DNA特异性染料,它们不仅可用于细胞核显像,也常用于线粒体观察。目前最常用的两种双苯并咪唑类染料Hoechst 33258和Hoechst 33342具有相似的光谱特性:均在350nm紫外光激发下产生461nm的蓝/青色荧光发射峰。

这类染料既适用于活细胞也适用于固定细胞染色,常作为核酸染料DAPI的替代选择。它们之间的主要区别是 Hoechst 33342 添加的乙基使其更亲脂,因此更能穿透完整的细胞膜。在某些应用中,Hoechst 33258 的渗透性较低。此外,通过建立标准荧光强度-DNA含量曲线,这些染料还可用于样本DNA含量的定量分析。

 

溶解方案(溶剂以说明书为准)

  0.1 mg 0.5 mg 1 mg 5 mg 10 mg
1 mM 177.958 µL 889.791 µL 1.78 mL 8.898 mL 17.796 mL
5 mM 35.592 µL 177.958 µL 355.916 µL 1.78 mL 3.559 mL
10 mM 17.796 µL 88.979 µL 177.958 µL 889.791 µL 1.78 mL
实验方案

染色细胞分析方案       

以下染色方案适用于大多数细胞类型,但需注意培养基成分、细胞密度、共培养细胞等因素均可能影响染色效果。实验器皿残留的洗涤剂可能导致假阳性染色(即便在没有细胞的溶液中也可能出现荧光物质)。

建议通过离心收集细胞后,用pH 7.4的缓冲盐溶液或培养基重悬(该pH条件最有利于染料结合)。贴壁细胞可直接在盖玻片或培养孔中原位染色。通常使用0.5-5 μM浓度范围的Hoechst染料,孵育15-60分钟。初次实验时,建议在推荐浓度范围内设置梯度实验以确定合适的染色条件。

 

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