Process for preparing anticencer active protein of thick muzzle syngnathus
An anti-tumor activity, crude protein technology, applied in the field of medicine, can solve the problem of no crude kiss sea dragon anti-tumor activity protein separation method and the like
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Embodiment 1
[0021] (1) The crude Kissia chinensis medicinal material is dried at low temperature, pulverized, and passed through a 40-mesh sieve.
[0022] (2) Take 200g of crude sea dragon powder, add 800ml of aqueous solution, homogenize 3 times for 30s each time, soak in a refrigerator at 4°C for 8 hours, centrifuge at 4800rpm for 10min, remove the supernatant, and obtain the crude sea dragon protein extract.
[0023] (3) Concentrate the crude sea dragon protein extract obtained in (2) to 200ml at 40°C under reduced pressure, put it on a HZ-801 macroporous resin separation column, elute with distilled water, collect the eluted components, and concentrate under reduced pressure at 40°C to 200ml to obtain the sea dragon protein isolate.
[0024] (4) Add ammonium sulfate powder to the sea dragon protein separation solution to 20% saturation while stirring, let it stand overnight at 4°C to allow it to fully precipitate, centrifuge at 10000rpm for 10min, collect the precipitate, and wash the...
Embodiment 2
[0032] (1) The crude Kissia chinensis medicinal material is dried at low temperature, pulverized, and passed through a 20-mesh sieve.
[0033] (2) Take 200g of crude sea dragon powder, add 1400ml of 45% ethanol solution, homogenate 3 times, each time for 30s, cold soak in 4℃ refrigerator for 6 hours, centrifuge at 4800rpm for 10min, remove the supernatant, and add 1000ml of the residue again 45 % ethanol, the same operation as above, the combined two extracts are the crude extract of sea dragon protein.
[0034] (3) Concentrate the crude sea dragon protein extract obtained in (2) to 300ml at 20°C under reduced pressure, put it on a HZ-801 macroporous resin separation column, elute with distilled water, collect the eluted components, and concentrate under reduced pressure at 50°C to 250ml to obtain the sea dragon protein isolate.
[0035] (4) Add ammonium sulfate powder to the sea dragon protein separation solution to 90% saturation while stirring, let it stand overnight at 4°...
Embodiment 3
[0041] (1) The crude Kissia chinensis medicinal material is dried at low temperature, pulverized, and passed through a 20-mesh sieve.
[0042] (2) Take 200g of crude sea dragon powder, add 1600ml of 90% ethanol solution, homogenize 3 times, each time for 30s, cold soak in 4°C refrigerator for 6 hours, centrifuge at 4800rpm for 10min, remove the supernatant, which is the crude sea dragon protein Extraction.
[0043] (3) Concentrate the crude sea dragon protein extract obtained in (2) to 300ml at 60°C under reduced pressure, put it on a HZ-801 macroporous resin separation column, elute with distilled water, collect the eluted components, and concentrate under reduced pressure at 50°C to 250ml to obtain the sea dragon protein isolate.
[0044] (4) Add ammonium sulfate powder to the sea dragon protein separation solution to 55% saturation while stirring, let it stand overnight at 4°C to allow it to fully precipitate, centrifuge at 10000rpm for 10min, collect the precipitate, and ...
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