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3520-43-2

中文名称 JC-1
英文名称 JC-1
CAS 3520-43-2
分子式 C25H27Cl4N4.I
分子量 652.228
MOL 文件 3520-43-2.mol
更新日期 2024/05/06 10:16:00
3520-43-2 结构式 3520-43-2 结构式

基本信息

中文别名
化合物JC-1
可见光吸收剂515
JC-1(线粒体膜电位探针)
线粒体膜电位荧光探针JC-1
5,5',6,6'-四氯-1,1',3,3'-四乙基苯并咪唑羰花青碘化物
5,5',6,6'-四氯-1,1',3,3'-四乙基苯并咪唑羰花菁碘化物
CBIC2(3),5,5′,6,6′-TETRACHLORO-1,1′,3,3′-TETRAETHYL-IMIDACARBOCYANINE IODIDE
英文别名
JC-1
JC-1, >95%
JC-1 jodide
CBIC2, >95%
-tetraethyl-5,5'
-tetrachloroimidacarbocyanine iodide
5,5',6,6'-TETRACHLORO-1,1',3,3'-*TETRAETHYBENZIMIDA
1,10,3,30-tetraethyl-5,50,6,60-tetrachloroimidacarbocyanine Iodide
5,5',6,6'-tetrachloro-1,1',3,3'-tetraethyl-imidacarbocyanine iodide
Imidacarbocyanine Iodide, 1,10,3,30-tetraethyl-5,50,6,60-tetrachloro-
所属类别
生物化工:细胞学常用试剂

物理化学性质

熔点275–278 ℃
储存条件room temp
溶解度溶于甲醇、N,N-二甲基甲酰胺、二甲亚砜
形态crystals
颜色深红色
最大波长(λmax)514nm
稳定性自购买之日起,在 -20°C 下按供应状态干燥保存最多 2 年。 DMSO 或蒸馏水中的溶液可在 4°C 下储存长达 1 年。不要冻结/解冻。仅通过过滤对溶液进行灭菌,而不是通过高压灭菌
生物领域应用Detectingmitochondrialmembrane potential,ABCB1,ABCC1,and ABCG2 transporters inhibitors,nucleic acid hybridization,prostate cancer; treating cellular death,Alzheimer’s disease; apoptosis assay; cytotoxicity assay; hematotoxicity
主要应用Langmuir-Blodgett films; lasing systems; nonlinear optical materials; photographic materials1,
InChIKeyFYNNIUVBDKICAX-UHFFFAOYSA-M

图谱信息

JC-1价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/04/30HY-15534JC-1
JC-1
3520-43-21mg700元
2024/04/30HY-15534JC-1
JC-1
3520-43-22mg1200元
2024/04/30HY-15534JC-1
JC-1
3520-43-25 mg2400元

常见问题列表

生物活性
JC-1 (CBIC2) 是荧光亲脂性羰花青染料,用于测量线粒体膜电位。线粒体膜电位较高时, JC-1 在基质中汇聚形成聚合物 (J-aggregates),可以产生红色荧光 (Ex/Em=585/590 nm);线粒体膜电位较低时,JC-1 不能聚集在线粒体基质中,以单体形式存在产生绿色荧光 (Ex/Em=510/527 nm)。
体外研究

Guidelines (Following is our recommended protocol. This protocol only provides a guideline, and should be modified according to your specific needs).
Labeling of Cells:
1. Culture cells in 6-, 12- , 24-, or 96-well plates at a density of 5× 10 5 cells/mL. Incubate the cells according to your normal protocol.
2. Ensure that the JC-1 and DMSO has equilibrated to room temperature, and then prepare a 200 μM stock solution by dissolving the contents of one vial in 230 μL of the DMSO provided.
3. For the control tube, allow the vial of CCCP has come to room temperature, add 1 μL of CCCP (50 mM). Incubate cells at 37°C for 5 minutes.
4. Add 10 μL JC-1 (200 μM) per well to make the final concentration at 2 μM. Incubate cells at 37°C, 5% CO 2 , for 15-20 minutes. If additional labeling followed, for example with an annexin V, begin with step 2.a. If not, proceed with step 1.e.
5. After incubation, centrifuge cells for 3-4 minutes at 400× g at 4°C, carefully aspirate the supernant.
6. Wash cells twice with PBS (1×): add 2 mL PBS (1×) to suspend cells and vortex to mix thoroughly. Centrifuge cells for 3-4 minutes at 400× g at 4°C, carefully aspirate the supernant.
7. Add 500 μL PBS (1×) to suspend cells. Analyze sample on a flow cytometer, fluorescence microscopy, or fluorescence microplate reader.

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