Method for simply preparing DiI (1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate) microscopic particles and marking neurons
A production method and neuron technology, applied in the field of biomedical experiments, can solve the problems of high technical difficulty, complex production process and high cost, and achieve the effects of simple operation, simple production and low cost
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[0031] The present invention will be described in further detail below in conjunction with the accompanying drawings and specific embodiments given by the inventor.
[0032] see Figure 1 to Figure 4 As shown, the method for labeling neurons with DiI microparticles includes 4 steps, namely, preparation of brain slices, preparation of DiI particles, embedding of DiI particles, and incubation of brain slices.
[0033] (1) Brain slice production.
[0034] The brain slices used to label neurons can be live or fixed brain slices, which are performed according to the brain slice patch clamp or immunohistochemical brain slice preparation techniques. Both brain slices must be sliced with a vibrating microtome with a thickness of 200-350 microns. Live brain slices were excised and incubated in oxygenated artificial cerebrospinal fluid (aCSF), while fixed isolated brain slices were placed in paraformaldehyde fixative solution with a mass volume concentration of 0.015-0.02 g / ml.
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