Formula constituted by cytokine and compound, its action of promoting nerve regeneration and action of researching and diagnosing nervous system disease
A cytokine, nerve regeneration technology, applied in diagnosis and treatment, prescription in the field of nervous system disease research
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Embodiment 1
[0087] Preparation of the prescription composed of cytokines and compounds of the present invention: take 1 mg of hydrocortisone, dissolve it in 10 ml of absolute ethanol, and prepare it as a 0.01% mother liquor; weigh 1 mg of progesterone, dissolve it in 10 ml of absolute ethanol, Prepare 0.01% mother liquor; weigh 100mg of insulin, dissolve in 10ml double-distilled water, and prepare 1% mother liquor; weigh 100mg of bovine serum albumin, dissolve in 10ml double-distilled water, and prepare 1% mother liquor; weigh Transferrin 2g, dissolved in 10ml double-distilled water, was prepared as 20% mother liquor; putrescine 300mg was dissolved in 10ml double-distilled water, and 3% mother liquor was prepared; 20mg triiodothyronine was weighed, dissolved In 10ml double-distilled water, prepare 0.2% mother liquor; weigh 1mg of sodium selenite, dissolve in 10ml double-distilled water, and prepare 0.01% mother liquor; dissolve 100μg EGF in 1ml double-distilled water, prepare 0.01% mother ...
Embodiment 2
[0089] Preparation of the prescription composed of cytokines and compounds of the present invention: dissolve 10 μg BDNF in 100 μl double distilled water to prepare a 0.01% mother solution; dissolve 10 μg NGF in 100 μl double distilled water to prepare a 0.01% mother solution; On the basis of the ingredients made in 1, BDNF was added to make the final concentration 2.5×10 -4 %; then add NGF to make the final concentration 5×10 -4 %. Mix evenly, make up to volume with double distilled water, and make the prescription of the present invention.
Embodiment 3
[0090] Example 3 Induced primary cortex and spinal cord neuron division experiment
[0091] Rat spinal cord and cortical neurons were isolated, and then a large dose of cytarabine was added to remove neural stem cells and other dividing cells. Then Nestin, GFAP and NSE immunocytochemical examination was used to confirm that there were no Nestin immunopositive cells, and primary neuron cells accounted for more than 95% of the total cells. Then add the recipe of cytokines and compounds obtained in Example 1 to induce neuron division. As a result (see FIG. 1 ), it was found that quite a lot of neurons were in the M phase (mitotic phase). The images show primary cortical and spinal cord neurons at different stages of mitosis.
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