Catalog No. B7755

Calcein AM (Calcein acetoxymethyl ester)

(别名:Calcein-AM; 钙黄绿素AM)

一种能渗透细胞的染料,可用于测定大多数真核细胞的活力。

Calcein AM (Calcein acetoxymethyl ester)
规格价格货期数量
1mg
¥3050.00
现货
CAS号:148504-34-1纯度:98.00%
仅用于科研,不用于诊疗。未经明确授权不得转售。
A
021-55669583sales@apexbio.cnAPExBIO

特色产品

Annexin V-FITC/PI Apoptosis Kit
Annexin V-FITC/PI Apoptosis Kit
用于双染检测细胞凋亡和坏死
- 在10-20分钟内完成染色
- 适用于流式细胞仪和荧光显微镜检测
- 准确区分活细胞/凋亡细胞/坏死细胞
Phos binding reagent (Phosbind) acrylamide
Phos binding reagent (Phosbind) acrylamide
分离和检测磷酸化/非磷酸化蛋白
- 新型的磷酸盐结合标签和功能分子
- 用于免疫印迹和质谱分析等后续操作
- 适用于30 KDa-130 KDa大小的蛋白
Cell Counting Kit-8 (CCK-8)
Cell Counting Kit-8 (CCK-8)
用于细胞增殖和细胞毒性试验
- 比MTT,MTS或WST-1更敏感
- 对细胞无毒性
- 步骤更简单,无需有机溶剂
Cy5 TSA Fluorescence System Kit
Cy5 TSA Fluorescence System Kit
Cy5荧光标记的酪胺信号放大系统
- 检测ICC/IHC/ISH中的低丰度靶点
- 可将信号灵敏度提高100倍
- 同时保持稳定的特异性和分辨率
EZ Cap™ Cy5 Firefly Luciferase mRNA (5-moUTP)
EZ Cap™ Cy5 Firefly Luciferase mRNA (5-moUTP)
用于观察mRNA运送,定位,翻译
- 具有Cap1结构的荧光素酶mRNA
- 提供更高的转录效率并抑制免疫激活
- 使用5-moUTP和Cy5-utp修饰
HotStart™ 2X Green qPCR Master Mix
HotStart™ 2X Green qPCR Master Mix
用于荧光定量目标DNA或cDNA
- 通过热启动机制优化扩增特异性
- 优异的扩增效率、可重复性和稳定性
- 卓越的灵敏度和准确性,操作简单
HyperScribe™ T7 High Yield Cy5 RNA Labeling Kit Plus
HyperScribe™ T7 High Yield Cy5 RNA Labeling Kit Plus
高效的Cy5修饰RNA转录试剂盒
- 适合原位/Northernblot杂交实验
- 优化的缓冲液和T7 RNA聚合酶混合物
- 20 μL反应体系可获得更高的RNA产量

产品描述

Calcein AM (Calcein acetoxymethyl ester),中文名称钙黄绿素乙酰氧基甲酯,能够轻易穿透活细胞膜,通过细胞内酯酶水解,在活细胞中变成荧光钙黄绿素。是一种对活细胞进行荧光标记的绿色荧光探针。Calcein AM是在Calcein (钙黄绿素)的基础上引入了乙酰氧基甲酯(AM)基团,增加了疏水性,因此能够轻易穿透活细胞膜。Calcein AM本身并无荧光,一旦进入细胞后被细胞内的酯酶水解生成具有强负电荷的不能通透细胞膜的极性分子钙黄绿素(Calcein),从而被滞留在细胞内,并发出强绿色荧光[1]。由于Calcein AM的细胞毒性非常低,几乎不会影响正常细胞的功能,而且对pH值敏感性低[2],因此是目前染活细胞的最理想荧光探针之一。

由于死细胞缺乏酯酶,Calcein AM仅用于对活细胞的活力测试和短期标记,而染核酸的红色荧光染料碘化丙啶(Propidium Iodide, PI)由于不能穿透活细胞的细胞膜而只能染细胞膜完整性被破坏的死细胞,Calcein和PI-DNA都可被490 nm激发,因此Calcein AM常常与碘化丙啶联合使用,同时对活细胞和死细胞进行荧光染色[3]。用545 nm激发,仅可观察到死细胞。

Calcein AM可以应用于大多数的哺乳动物细胞。也有研究显示Calcein AM可以用于某些植物细胞如拟南芥(Arabidopsis)的根边缘样细胞[4]及某些酵母如Pichia anomala和Saccharomyces cerevisiae[5]。某些寄生虫如Leishmania由于细胞膜组分的原因,Calcein AM不能进入活细胞,但却可以进入凋亡早期的寄生虫细胞,从而与PI联用用于检测凋亡早期的寄生虫[6]。由于真菌和细菌有细胞壁,会阻碍Calcein AM进入细胞,因此Calcein AM不适合用于真菌和细菌。

References:

[1] Giordano G, Hong S, Faustman EM, et al. Measurements of cell death in neuronal and glial cells. Methods Mol Biol. 2011;758:171-8.

[2] Neri S, Mariani E, Meneghetti A, et al. Calcein-acetyoxymethyl cytotoxicity assay: standardization of a method allowing additional analyses on recovered effector cells and supernatants. Clin Diagn Lab Immunol. 2001;8(6):1131–1135.

[3] Kuksin D, Kuksin CA, Qiu J, et al. Cellometer image cytometry as a complementary tool to flow cytometry for verifying gated cell populations. Anal Biochem. 2016 Jun 15;503:1-7.

[4] Vicré M, Santaella C, Blanchet S, et al. Root border-like cells of Arabidopsis. Microscopical characterization and role in the interaction with rhizobacteria. Plant Physiol. 2005;138(2):998–1008.

[5] Prudêncio C, Sansonetty F, Sousa MJ, et al. Rapid detection of  efflux pumps and their relation with drug resistance in yeast cells. Cytometry. 2000 Jan 1;39(1):26-35.

[6] Basmaciyan L, Azas N, Casanova M. Calcein+/PI- as an early apoptotic feature in Leishmania. PLoS One. 2017 Nov 7;12(11):e0187756.

产品性质

物理外观A crystalline solid
CAS号148504-34-1
分子式C46H46N2O23
分子量994.86
小分子别名Calcein-AM
化学名称tetrakis(acetoxymethyl) 2,2',2'',2'''-(((3',6'-diacetoxy-3-oxo-3H-spiro[isobenzofuran-1,9'-xanthene]-4',5'-diyl)bis(methylene))bis(azanetriyl))tetraacetate
溶解度Soluble in DMSO
SMILESO=C1O[C@@]2(C3=CC=CC=C31)C(C=C4)=C(C(CN(CC(OCOC(C)=O)=O)CC(OCOC(C)=O)=O)=C4OC(C)=O)OC5=C2C=CC(OC(C)=O)=C5CN(CC(OCOC(C)=O)=O)CC(OCOC(C)=O)=O
存储条件-20°C
运输条件蓝冰

产品应用 (实验数据来自文献,APExBIO并未验证,仅供参考)

IC50和靶点

生物活性描述Calcein-AM 是一种细胞渗透性荧光染料;用于测定细胞活力。

质量控制

操作说明

APExBIO 顾客使用本产品发表的 9 篇科研文献

1. Jiawei Hong, Zhongkai Yu, et al. "Silk Fibroin Ionotronics for High-Performance Wearable Perovskite LEDs." ACS Nano. 2026 May 21. PMID: 42165121

2. Ziwei Zhou, Si Chen, et al. "EGFR TKIs suppress MUC1 glycosylation through the PI3K/AKT/SP1/C1GALT1 pathway to enhance TnMUC1 CAR-T efficacy in EGFR-mutant NSCLC." Cell Rep Med . 2025 Jul 15;6(7):102199. PMID: 40562040

3. Hang Zhao, Bo Yu, et al. "Electrochemical‐Genetic Programming of Protein‐Based Magnetic Soft Robots for Active Drug Delivery." Adv Sci (Weinh) . 2025 Jul;12(27):e2503404. PMID: 40298906

4. Jiamin Qin, Guojuan Fan, et al. "Dynamic Covalent Bond-Based Nanoassembly of Curcumin to Enhance the Selective Photothermal Therapy for Tumor Treatment." Int J Nanomedicine. 2025 Mar 30:20:3861-3875. PMID: 40181832

5. Shanshan Jiang, Wanyu Li, et al. "Oxygen-regulated enzymatic nanoplatform for synchronous intervention in glycolysis and oxidative phosphorylation to augment antitumor therapy." J Control Release. 2025 May10:381:113594. PMID: 40024344

6. Rong Ma, Zhengwei Sun, Zhihui Xu. "Injectable adhesive hydrogel microspheres encapsulating VEGFA-high expression MSC exosomes for the treatment of intrauterine adhesions." Chemical Engineering Journal Volume 526, 15 December 2025, 171410

7. Yihan Zhang, Yubing Hu, et al. "Holographic hydrogel bandage sensor for continual monitoring of wound healing." Sensors & Diagnostics 2025

8. Mayur Aalhate, Srushti Mahajan, et al. "Chondroitin Sulfate-Mediated Targeted Delivery of Docetaxel and Silibinin-Loaded Nanoparticles for Amelioration of Anticancer Efficacy in Breast Cancer." ACS Applied Bio Materials. August 25, 2025

9. Yin Ni, Bang-Chuan Hu, et al. "Interruption of neutrophil extracellular traps formation dictates host defense and tubular HOXA5 stability to augment efficacy of anti-Fn14 therapy against septic AKI." Theranostics. 2021 Sep 13;11(19):9431-9451. PMID: 34646379

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