Dilinoleyl DiI (cell membrane orange red fluorescent probe)

​Dilinoleyl DiI, also known as fast DiI, has the same absorption and emission wavelength as DiI. Because dlinoleyl DiI contains unsaturated hydrocarbon chains, the lateral diffusion speed of dilinoleyl DiI on the cell membrane is faster than that of DiI. Because of this property, it is widely used in tracking neuronal tissues. After dilinoleyl DiI staining, paraformaldehyde (methanol and other reagents cannot be used) can be fixed, but permeabilization after staining is not recommended. In addition, after fixed permeabilization (permeabilization with 0.1% TritonX-100 at room temperature), the plasma membrane staining can also be well performed. At 100 per use μ L of dyeing working solution with a concentration of 10 μ According to m calculation, 5 mg of working solution can be used for 5400 times.Product parameters：Ex/Em (MeOH) = 549/565 nmMatters needing attention：1. please centrifuge the product to the bottom of the tube immediately before use, and then conduct subsequent experiments. 2. when dilinoleyl DiI is used to stain fixed cells or tissue samples, 4% paraformaldehyde prepared in PBS is usually used for fixation. The use of other inappropriate fixatives will lead to high fluorescence background. 3. fluorescent dyes have quenching problems. Please try to avoid light to slow down fluorescence quenching. 4. for your safety and health, please wear experimental clothes and disposable gloves.Scope of application：Cell membrane fluorescent dye ; anterograde and retrograde tracing of neurons ; long-term cell tracingUsage:1. Preparation of staining solution(1) Preparation of storage solution: The storage solution is prepared with anhydrous DMSO or EtOH, with a concentration of 1-10 mM.Note: Unused storage liquids should be packaged and stored at -20 ℃ to avoid repeated freeze-thaw cycles.(2) Preparation of working solution: Dilute the storage solution with a suitable buffer (such as serum-free medium, HBSS or PBS) and prepare a concentration of 1-10 μ M's working fluid.Note: It is recommended to optimize the final concentration of the working solution based on different cell lines and experimental systems. It is recommended to start exploring the optimal concentration within a range of 10 times the recommended concentration.2. Suspension cell staining(1) Add an appropriate volume of staining solution and resuspend the cells to a density of 1 × 106/mL.(2) Incubate cells at 37 ℃ for 5-20 minutes, and the optimal culture time varies for different cells. 20 minutes can be used as the starting incubation time, and then the system can be optimized to obtain a uniform labeling effect.(3) After incubation, centrifuge at 1000-1500 rpm for 5 minutes. Pour the supernatant and slowly add the growth culture medium preheated at 37 ℃ again to resuspend the cells.(4) Repeat step (3) more than twice.3. Staining of adherent cells(1) Cultivate adherent cells on sterile cover slips.(2) Remove the cover glass from the culture medium and absorb excess culture medium, but keep the surface moist.(3) Add 100 to one corner of the cover glass μ Gently shake the dye working solution of L to evenly cover all cells with the dye.(4) Incubate cells at 37 ℃ for 5-20 minutes, and the optimal culture time varies for different cells. 20 minutes can be used as the starting incubation time, and then the system can be optimized to obtain a uniform labeling effect.(5) Dry the dye working solution, wash the cover glass with culture medium 2-3 times, cover all cells with preheated culture medium each time, incubate for 5-10 minutes, and then dry the culture medium. But keep the surface moist.4. Result detectionThe sample can be detected in the culture medium and analyzed by fluorescence microscopy imaging or flow cytometry. Molecular Formula: C59H89ClN2O4. Molecular Weight: 925.80.