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JC-1 (solution)  (Synonyms: CBIC2 (solution))

目录号: HY-15534Y
产品使用指南 技术支持

JC-1 (solution) (CBIC2 (solution)) 是一种广泛用于检测线粒体膜电位的理想荧光探针。JC-1 染料以电势依赖性的方式积聚在线粒体内,可以用来检测细胞、组织或纯化的线粒体膜电位。正常线粒体内,JC-1 聚集在线粒体基质中形成聚合物,聚合物发出强烈的红色荧光 (Ex=585 nm, Em=590 nm) ;在线粒体膜电位较低时,JC-1不能聚集在线粒体的基质中,产生绿色荧光 (Ex=510 nm, Em=527 nm) 。

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JC-1 (solution)

JC-1 (solution) Chemical Structure

CAS No. : 3520-43-2

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规格 价格 是否有货
978.34 μg (1.5 mM * 1 mL in DMSO) ¥1070
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1.95 mg (1.5 mM * 2 mL in DMSO) ¥1600
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JC-1 (solution) 的其他形式现货产品:

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Other Forms of JC-1 (solution):

MCE 顾客使用本产品发表的 157 篇科研文献

IF

    JC-1 (solution) purchased from MCE. Usage Cited in: Bioact Mater. 2022 Aug 11;21:20-31.  [Abstract]

    JC-1 (20 min at 37 °C in dark) staining is used to analyze mitochondrial membrane in H9C2 cells.

    JC-1 (solution) purchased from MCE. Usage Cited in: ACS Nano. 2022 Apr 26;16(4):6064-6079.  [Abstract]

    To investigate the mitochondrial membrane potential, ACCO is stained with JC-1 for 30 min, washed with PBS, and analyzed by flow cytometry using 488 nm excitation with 530/30 and 585/42 nm band-pass filters.

    JC-1 (solution) purchased from MCE. Usage Cited in: Pharmacol Res. 2022 May;179:106123.  [Abstract]

    Mitochondrial membrane potential (Δψm) is measured with fluorochrome dye JC-1 (15 μM; 37 °C for 30 min in darkness). Flow cytometry is used to measure red (aggregation of JC-1) and green (monomeric JC-1) fluorescence intensity in HUVECs.

    JC-1 (solution) purchased from MCE. Usage Cited in: Small. 2021 Aug;17(32):e2101368.  [Abstract]

    Laser scanning confocal fluorescence microscopy images of JC-1, LysoTracker Red DND-99, and AO staining for determining mitochondrial membrane potential, lysosomal deacidification, and lysosomal membrane permeabilization, respectively.

    JC-1 (solution) purchased from MCE. Usage Cited in: Small. 2021 Feb;17(7):e2005865.  [Abstract]

    In 4T1 cells, A549 cells, and HeLa cells, cells are treated with JC-1 (5 µg/mL) for 20 min in the darkness, the fluorescence is observed by flow cytometry and the fluorescent color of the cells was observed with a fluorescence microscope, respectively

    JC-1 (solution) purchased from MCE. Usage Cited in: Small. 2021 Feb;17(7):e2005865.  [Abstract]

    In 4T1 cells, A549 cells, and HeLa cells, cells are treated with JC-1 (5 µg/mL) for 20 min in the darkness, the fluorescence is observed by flow cytometry and the fluorescent color of the cells was observed with a fluorescence microscope, respectively

    JC-1 (solution) purchased from MCE. Usage Cited in: Mol Cancer. 2019 Apr 10;18(1):85.  [Abstract]

    KRA-533 induces caspase 3 activation and reduces mitochondrial membrane potential in NSCLC cells. The measurement of mitochondrial membrane potential by JC-1 staining.

    JC-1 (solution) purchased from MCE. Usage Cited in: Small. 2019 Sep;15(36):e1902642.  [Abstract]

    H9C2 cells are rinsed with pre-cooled PBS for 3 times and collected in PBS buffer containing 10 µg/mL JC-1 probe. After incubation for 20 min in dark place, cells are rinsed with PBS twice by centrifugation to remove the supernatant. Finally, H9C2 cell pellets suspended in PBS are analyzed by a flow cytometric analyzer.

    JC-1 (solution) purchased from MCE. Usage Cited in: New J Chem. 2017 41(23).

    Measurement of mitochondria membrane potential by JC-1 staining. HeLa cells are incubated with or without WOs for 24 h, followed by NIR irradiation for NIR and WOs + NIR groups.
    • 生物活性

    • 纯度 & 产品资料

    • 参考文献

    生物活性

    JC-1 (solution) (CBIC2 (solution)) is an ideal fluorescent probe widely used to detect mitochondrial membrane potential. JC-1 accumulates in mitochondria in a potential dependent manner and can be used to detect the membrane potential of cells, tissues or purified mitochondria. In normal mitochondria, JC-1 aggregates in the mitochondrial matrix to form a polymer, which emits strong red fluorescence (Ex=585 nm, Em=590 nm); When the mitochondrial membrane potential is low, JC-1 cannot aggregate in the matrix of mitochondria and produce green fluorescence (ex=510 nm, em= 527 nm)[1].

    体外研究
    (In Vitro)

    JC-1 染色液的配制
    1.1 制备储存液
    用 DMSO 配制 5 mg/mL 的 JC-1。如用 1 mL DMSO 溶解 5 mg JC-1。
    注:1) JC-1 储存液建议分装后于 -20℃ 或 -80℃ 避光保存。
    1.2 工作液的配制
    用预热好的无血清细胞培养基或 PBS 稀释储存液,配制成 1-20 μg/mL 的 JC-1 工作液。
    注:1) 请根据实际情况调整 JC-1 工作液浓度,且现用现配。
    2) 如果 JC-1 进入细胞的效果不好,可向工作也液中加入适量 20% Pluronic F127 溶液,终浓度为 0.02-0.05%,Pluronic F127 可以防止 JC-1 在缓冲液中聚合并帮助其进入细胞。
    JC-1染色
    1) 以6孔板为例进行细胞铺板,密度为 5×105 cells/mL。37℃,5% CO2 培养箱培养过夜。
    注:进行凋亡诱导时的细胞密度建议不超过 1×106/mL,也可根据自己的细胞类型培养至合适的密度。
    2) 取 0.5 mL 细胞悬液至无菌的离心管内。
    3) 400 g 离心 3-5 min;弃上清。
    4) 用 1 mL JC-1 工作液重悬细胞,于 37℃,5% CO2 培养箱孵育 15-30 min。
    5) 室温条件 400 g 离心 5 min;吸掉上清。
    6) 用 2 mL 细胞培养液或者缓冲液重悬细胞,之后室温条件 400 g 离心 5 min;弃上清,重复两次。
    7) 用 1 mL 新鲜培养液或者缓冲液重悬细胞,立刻进行后续的流式分析或荧光显微镜观察。
    8) 数据分析 (流式细胞仪) :含有红色 JC-1 聚集物的健康细胞线粒体用 FL2 通道检测;含有绿色 JC-1 单体的凋亡或不健康细胞用 FL1 (FITC) 通道检测。
    注:若用于酶标仪检测,用 300 μL 缓冲液重悬细胞;然后按照每孔 100 μL 的量将染色好的细胞转移到不透光的 96 孔板内,即可进行荧光酶标板分析。

    MCE has not independently confirmed the accuracy of these methods. They are for reference only.

    分子量

    652.23

    Formula

    C25H27Cl4IN4

    CAS 号
    运输条件

    Room temperature in continental US; may vary elsewhere.

    储存方式

    Please store the product under the recommended conditions in the Certificate of Analysis.

    纯度 & 产品资料
    参考文献
    • 摩尔计算器

    • 稀释计算器

    The molarity calculator equation

    Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

    质量   浓度   体积   分子量 *
    = × ×

    The dilution calculator equation

    Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

    This equation is commonly abbreviated as: C1V1 = C2V2

    浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
    × = ×
    C1   V1   C2   V2
    Help & FAQs
    • Do most proteins show cross-species activity?

      Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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