Hoechst 33258 analog 3

目录号: GC36241纯度: >99.50%

Hoechst 33258 analog 3是核酸染色剂Hoechst 33258的类似物,与dsDNA结合后发出蓝色荧光,最大激发光/发射光为365/458nm


Hoechst 33258 analog 3
Cas No.: 23554-98-5
规格价格库存数量操作
1mg¥898.00现货
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产品描述 Description

Hoechst 33258 analog 3 are part of a family of blue fluorescent dyes used to stain DNA.IC50 Value:Target: These Bis-benzimides were originally developed by Hoechst AG, which numbered all their compounds so that the dye Hoechst 33342 is the 33342nd compound made by the company. There are three related Hoechst stains: Hoechst 33258, Hoechst 33342, and Hoechst 34580. The dyes Hoechst 33258 and Hoechst 33342 are the ones most commonly used and they have similarexcitation/emission spectra. Both dyes are excited by ultraviolet light at around 350 nm, and both emit blue/cyan fluorescent light around anemission maximum at 461 nm. Unbound dye has its maximum fluorescence emission in the 510-540 nm range. Hoechst dyes are soluble in water and in organic solvents such as dimethyl formamide or dimethyl sulfoxide. Concentrations can be achieved of up to 10 mg/mL. Aqueous solutions are stable at 2-6 °C for at least six months when protected from light. For long-term storage the solutions are instead frozen at ≤-20 °C.The dyes bind to the minor groove of double-stranded DNA with a preference for sequences rich in adenine andthymine. Although the dyes can bind to all nucleic acids, AT-rich double-stranded DNA strands enhance fluorescence considerably.Hoechst dyes are cell-permeable and can bind to DNA in live or fixed cells. Therefore, these stains are often called supravital, which means that cells survive a treatment with these compounds. Cells that express specific ATP-binding cassette transporter proteins can also actively transport these stains out of their cytoplasm.

[1]. Portugal J, Waring MJ. Assignment of DNA binding sites for 4',6-diamidine-2-phenylindole and bisbenzimide (Hoechst 33258). A comparative footprinting study. Biochimica et Biophysica Acta 949 (2): 158-68. [2]. Latt SA, Stetten G, Juergens LA, Recent developments in the detection of deoxyribonucleic acid synthesis by 33258 Hoechst fluorescence. The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 23 (7): 493-505. [3]. a b c "Hoechst Stains". Invitrogren (Molecular Probes).

实验参考方法 Experimental Reference Method

本方案仅提供一个指导,请根据您的具体需要进行修改。
1、制备Hoechst染色液
(1) 配制Hoechst染料储存液: 使用DMSO溶解固体粉末,配置成10mg/mL的Hoechst染料储存液。
注意: Hoechst储存液建议分装后于-4℃或-20℃避光保存,避免反复冻融。
(2)工作液制备:使用预热的无血清培养基或缓冲液(如HBSS或PBS)稀释储存液,配制浓度为10μg/mL的Hoechst工作液。
注意: 请根据实际情况调整 Hoechst 工作液浓度,现用现配。
2、细胞染色
2.1 悬浮细胞(以6孔板为例)
(1)悬浮细胞经1000g离心3-5min。弃去上清液,使用PBS清洗两次,每次5分钟。
(2)加入1mL的Hoechst染料工作液,室温避光孵育5-10 min分钟。
(3)孵育结束后,经1000g离心5分钟,去除上清液,加入PBS清洗2-3次,每次5分钟。
(4)使用无血清细胞培养基或PBS重悬细胞,通过荧光显微镜或流式细胞技术进行观察。
2.2 贴壁细胞
(1)在无菌盖玻片上培养贴壁细胞。
(2)从培养基中移走盖玻片,吸出过量的培养基,将盖玻片放在潮湿的环境中。
(3)从盖玻片的一角加入100μL的Hoechst染料工作液,轻轻晃动使染料均匀覆盖所有细胞,室温避光孵育5-15min分钟。
(4)吸弃染料工作液,使用培养液洗盖玻片2~3次,通过荧光显微镜进行观察。
3.显微镜检测:Hoechst 33258的激发/发射光分别为365⁄458nm。

注意事项:
①对于固定的细胞或组织样品的染色,固定后需漂洗去除固定剂;
②Hoechst 33258染色通常在其他染色后进行,如果不需要进行其它染色,则直接进行Hoechst 33258染色;
③为减缓荧光淬灭,建议使用抗荧光淬灭封片剂;
④荧光染料均存在淬灭问题,请尽量注意避光;
⑤Hoechst 33258对人体有一定刺激性,为了您的安全和健康,请穿实验服并戴一次性手套操作。
References:
[1]. K D Harshman, P B Dervan. Molecular recognition of B-DNA by Hoechst 33258. 1985 Jul 11;13(13):4825-35. doi: 10.1093/nar/13.13.4825.

产品文档 Product Documents

Purity:>99.50%

化学性质Chemical Properties

CAS 号
23554-98-5
SMILES
CN1CCN(C2=CC=C3N=C(C4=CC=C5N=C(C6=CC=C(C)C=C6)NC5=C4)NC3=C2)CC1
分子式
C26H26N6
分子量
422.52 g/mol
溶解性
DMSO : 3.57 mg/mL (8.45 mM; Need ultrasonic (<70°C))
保存条件
Store at -20°C
General tips
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至 37°C,然后在超声波浴中震荡一段时间。
Shipping Condition
评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备 RT,或根据请求配备蓝冰。

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