Cell growth regulating factor G and its preparation process
A cell growth regulator, gene technology, applied in the field of biomedicine, can solve problems such as limitations, and achieve the effect of TC enhancement
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Embodiment 2
[0015] Example 2, Gram-negative cocci were first screened and the strains were frozen and preserved, and the strains were routinely cultured at a temperature of 9°C. After the strains were fully cultured, they were filtered three times successively to remove impurities and harmful bacteria, leaving beneficial bacteria fragments , which is to extract natural genes; take 1 μg of beneficial bacteria fragments, namely natural genes, add 3 mg of cysteine quantitatively to it, measure the content and pass the safety test, and seal it in GMP standard water or freeze-dried powder to form natural cell growth Regulatory factor G, after the finished product passes the inspection, it will be printed and packaged.
Embodiment 3
[0016] Example 3, the Gram-negative bacilli were first screened and the strains were frozen and preserved, and the strains were conventionally cultured at a temperature of 20°C. After the strains were fully cultivated, they were filtered twice successively to remove impurities and harmful bacteria, leaving beneficial bacteria Fragments are the extraction of natural genes; take 1 μg of beneficial bacteria fragments, that is, natural genes, add 8 mg of cysteine quantitatively to them, measure the content, and after safety testing, seal them in GMP standard water or freeze-dried powder to form natural cells Growth Regulatory Factor G, after the finished product passes the inspection, it will be printed and packaged.
Embodiment 4
[0017] Example 4, the Gram-positive bacilli were first screened and the strains were frozen and stored, and the strains were conventionally cultured at a temperature of 38°C. After the strains were fully cultivated, they were filtered once to remove impurities and harmful bacteria, leaving beneficial bacteria fragments. That is to extract natural genes, usually the more times of filtering, the purer the remaining (extracted) beneficial bacteria fragments, that is, the natural genes. Take 1 μg of beneficial bacteria fragments, that is, natural genes, add 20 mg of cysteine quantitatively to it, measure the content and pass the safety test, seal and seal the natural cell growth regulatory factor G in GMP standard water solution or freeze-dried powder, and the finished product passes the inspection Finally, printing and packaging.
[0018] Other embodiments of the present invention can be freely configured within the range of 1 μg of natural gene, 1 μg—500 mg of cysteine.
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