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目錄:MedChemExpress LLC>>生化試劑>> Fluo-3AM | MCE

Fluo-3AM | MCE
  • Fluo-3AM | MCE
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更新時間:2023-06-15 09:30:17瀏覽次數(shù):161評價

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CAS 121714-22-5 純度 ≥99.0%
分子量 1129.85 分子式 C??H??Cl?N?O??
供貨周期 現(xiàn)貨 規(guī)格 1 mg
貨號 HY-D0716 應(yīng)用領(lǐng)域 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥
Fluo-3AM | MCEFluo-3 AM is a fluorecent Ca<sup>2+</sup> chelator, with high affinity for calcium. Fluo-3 AM can specifically identify intracellular calcium ions, with high sensitivity, low cytotoxicity, increased AM acetylmethyl ester can enter the cell well, after being sheared by the intracellular esterase stay in the cell to bind to calcium ions, produce strong fluorescence<sup>[1]</sup>.

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Fluo-3AM

CAS No. : 121714-22-5

產(chǎn)品活性:Fluo-3 AM is a fluorecent Ca2+ chelator, with high affinity for calcium. Fluo-3 AM can specifically identify intracellular calcium ions, with high sensitivity, low cytotoxicity, increased AM acetylmethyl ester can enter the cell well, after being sheared by the intracellular esterase stay in the cell to bind to calcium ions, produce strong fluorescence.

研究領(lǐng)域:Others

作用靶點:Fluorescent Dye

In Vitro: 1. Preparation of Fluo-3 AM working solution
1.1 Preparation of the stock solution
Dissolve 1 mg Fluo-3 AM in 135 μL DMSO to obtain 10 mM of stock solution.
Note: It is recommended to store the stock solution at -20℃?or -80℃?away from light and avoid repetitive freeze-thaw cycles.
1.2 Preparation of Fluo-3 AM working solution
Dilute the stock solution in HBSS to obtain 1-10 μM of? working solution.
Note: Please adjust the concentration of Fluo-3 AM?working solution according to the actual situation.
2. Cell staining
2.1 Suspension cells (6-well plate)
a. Centrifuge at 1000 g at 4℃?for 3-5 minutes and then discard the supernatant. Wash twice with PBS, 5 minutes each time. The cell density is 1×106/mL
b.Add 1 mL of working solution, and then incubate at room temperature for 5-30 minutes.
c. Centrifuge at 400 g at 4℃?for 3-4 minutes and then discard the supernatant.
d. Wash twice with PBS, 5 minutes each time.
e. Resuspend cells with serum-free cell culture medium or PBS. Observation by fluorescence microscopy or flow cytometry.
2.2 Adherent cells
a. Culture adherent cells on sterile coverslips.
b. Remove the coverslip from the medium and aspirate excess medium.
c. Add 100 μL of working solution, gently shake it to completely cover the cells, and then incubate at room temperature for 5-30 minutes.
d. Wash twice with medium, 5 minutes each time. Observation by fluorescence microscopy.
Storage
-20℃, 1 year
Protect from light

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