Hoechst 33342 溶液 (20 mM)
Thermo Scientific™

Hoechst 33342 溶液 (20 mM)

Thermo Scientific Pierce Hoechst 33342 荧光染料是一种高质量 Hoechst 染料溶液,可用于细胞成像技术中 DNA 和细胞核的固定细胞和活细胞荧光染色了解更多信息
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货号数量
622495 mL
货号 62249
价格(CNY)
1,557.00
Online Exclusive
Ends: 31-Dec-2026
2,162.00
共减 605.00 (28%)
Each
数量:
5 mL
价格(CNY)
1,557.00
Online Exclusive
Ends: 31-Dec-2026
2,162.00
共减 605.00 (28%)
Each
Thermo Scientific Pierce Hoechst 33342 荧光染料是一种高质量 Hoechst 染料溶液,可用于细胞成像技术中 DNA 和细胞核的固定细胞和活细胞荧光染色。

Hoechst 33342 荧光染料的特点:

Hoechst 染料—专用于 DNA(即真核细胞的核)的蓝色荧光染料
便利—以易于使用的 Hoechst 染料溶液 (20 mM) 形式提供
细胞成像—细胞渗透性染料可有效用于固定细胞和活细胞染色
复染剂—适用于与荧光显微镜检查或高内涵筛选 (HCS) 荧光抗体的特定靶标检测配合使用

Hoechst 33342(2'-[4-乙氧基苯基]-5-[4-甲基-1-哌嗪基]-2,5'-bi-1H-苯并咪唑三盐酸化物三水合物)是一种细胞渗透性 DNA 染色剂,可被紫外光激发并在 460 至 490 nm 处发射蓝色荧光。Hoechst 33342 优先与 DNA 的腺嘌呤-胸腺嘧啶 (A-T) 区域结合。该染料可与 DNA 的小沟结合,展现出依赖于染料:碱基对比值的不同荧光发射光谱。

Hoechst 荧光染料的特性
作为荧光成像方法的复染剂,Hoechst 染料可兼容荧光素罗丹明染料标记的抗体及其他探针以及 Thermo Scientific DyLight Fluor。稳定的 20 mM 水性储备液基本可直接使用。

Hoechst33342 用于活细胞或固定细胞和组织的细胞核的特异性染色。该染色剂通常与 5-溴-2'-脱氧尿苷 (BrdU) 标记结合使用,以区分凋亡细胞核的紧凑染色质,从而确定复制细胞并根据细胞 DNA 含量对细胞进行分类。Hoechst 33342 和碘化丙啶通常一起用于对细胞凋亡和细胞周期分布各个阶段同时进行流式细胞和荧光成像分析。
仅供科研使用。不可用于诊断程序。
规格
颜色蓝色
最大浓度20 mM
检测方法荧光
染料类型细胞通透性
发射497 nm
激发波长范围361 nm
适用于(应用)荧光标记
适用于(设备)荧光显微镜、高内涵仪器
形式液体
产品线Pierce
数量5 mL
运输条件室温
标签类型Fluorescent Dye
产品类型核酸染色剂
亚细胞定位细胞核/核仁
Unit SizeEach
内容与储存
收货后,在 4°C 下避光储存。

常见问题解答 (FAQ)

我有一份活细菌和血小板细胞的混合液,需要将其中的细菌分离出来。你们有什么建议吗?

血小板细胞没有DNA,而细菌含有DNA。因此,细胞通透型DNA染料会优先染色细菌而不染色血小板。我们建议使用Hoechst 33342染料。

DAPI和Hoechst 染料非常相似,该如何选用?

DAPI是一种非常普通的蓝色核复染荧光染料,能对固定和通透的细胞和组织的细胞核进行非常明亮的标记。遗憾的是,人们普遍认为它是介于半通透性到非通透性之间的染色剂,对活细胞的染色效果也不一致。Hoechst 33342染料是细胞通透性染料,与DAPI染色有相似的染色结合机制和荧光颜色;它是活细胞成像的首选,且对固定细胞的标记效果和DAPI一样好。

Is DAPI a good live-cell nuclear label?

DAPI is considered a semi-permeant/impermeant nucleic acid stain. Staining of nucleic is dependent upon the cell line in its performance. Some cell lines will label with DAPI, others not at all, and others label inconsistenly. Instead, we recommend using either Hoechst 33342 or Hoechst 33258, which have the same wavelength and binding mode as DAPI (at the A-T minor groove) but are readily cell-permeant.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

I want to label the nuclei of live cells and track them over time. Can I use DAPI for this?

We do not recommend doing this. DAPI is considered to be a semi-permeant/impermeant nucleic acid stain. DAPI staining of live cells may be inconsistent. It is best used as a counterstain for fixed samples. Other cell permeable nucleic acid stains, such as Hoechst or the SYTO dyes may affect cellular function.

For mammalian cells, we recommend using the CellLight Nucleus transduction reagents, available in CFP, GFP and RFP. With these reagents, the cells are transduced overnight in a single labeling step and the next day the nuclei will fluoresce. The label may be retained for 3-5 days and should not affect cell function. Cytoplasmic cell tracking dyes such as the CellTracker dyes may also be used.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

I have a mix of live bacteria and platelet cells, and I need to be able to separate out the bacteria. Do you have a suggestion?

Platelet cells don't have DNA, while bacteria do. Therefore, a cell-permeant, DNA-selective dye would preferentially stain the bacteria with limited staining of the platelets. We recommend using Hoechst 33342 dye.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

引用和文献 (10)

引用和文献
Abstract
Generation, transcriptome profiling, and functional validation of cone-rich human retinal organoids.
Authors:Kim S, Lowe A, Dharmat R, Lee S, Owen LA, Wang J, Shakoor A, Li Y, Morgan DJ, Hejazi AA, Cvekl A, DeAngelis MM, Zhou ZJ, Chen R, Liu W
Journal:Proc Natl Acad Sci U S A
PubMed ID:31072937
'Rod and cone photoreceptors are light-sensing cells in the human retina. Rods are dominant in the peripheral retina, whereas cones are enriched in the macula, which is responsible for central vision and visual acuity. Macular degenerations affect vision the most and are currently incurable. Here we report the generation, transcriptome ... More
Yin Yang 1 Orchestrates a Metabolic Program Required for Both Neural Crest Development and Melanoma Formation.
Authors:Varum S, Baggiolini A, Zurkirchen L, Atak ZK, Cantù C, Marzorati E, Bossart R, Wouters J, Häusel J, Tuncer E, Zingg D, Veen D, John N, Balz M, Levesque MP, Basler K, Aerts S, Zamboni N, Dummer R, Sommer L
Journal:Cell Stem Cell
PubMed ID:30951662
'Increasing evidence suggests that cancer cells highjack developmental programs for disease initiation and progression. Melanoma arises from melanocytes that originate during development from neural crest stem cells (NCSCs). Here, we identified the transcription factor Yin Yang 1 (Yy1) as an NCSCs regulator. Conditional deletion of Yy1 in NCSCs resulted in ... More
Semisynthetic biosensors for mapping cellular concentrations of nicotinamide adenine dinucleotides.
Authors:Sallin O, Reymond L, Gondrand C, Raith F, Koch B, Johnsson K
Journal:Elife
PubMed ID:29809136
We introduce a new class of semisynthetic fluorescent biosensors for the quantification of free nicotinamide adenine dinucleotide (NAD
Neuropsin (OPN5) Mediates Local Light-Dependent Induction of Circadian Clock Genes and Circadian Photoentrainment in Exposed Murine Skin.
Authors:Buhr ED, Vemaraju S, Diaz N, Lang RA, Van Gelder RN
Journal:Curr Biol
PubMed ID:31607531
Nearly all mammalian tissues have functional, autonomous circadian clocks, which free-run with non-24 h periods and must be synchronized (entrained) to the 24 h day. This entrainment mechanism is thought to be hierarchical, with photic input to the retina entraining the master circadian clock in the suprachiasmatic nuclei (SCN) and the SCN ... More
Ca
Authors:Li S, Lavagnino Z, Lemacon D, Kong L, Ustione A, Ng X, Zhang Y, Wang Y, Zheng B, Piwnica-Worms H, Vindigni A, Piston DW, You Z
Journal:Mol Cell
PubMed ID:31053472
Abnormal processing of stressed replication forks by nucleases can cause fork collapse, genomic instability, and cell death. Despite its importance, it is poorly understood how the cell properly controls nucleases to prevent detrimental fork processing. Here, we report a signaling pathway that controls the activity of exonuclease Exo1 to prevent ... More