Ocean Sipunculus nudus plasmin and its preparation and application
A kind of technology of square star worm and ocean star worm, which can be applied in the fields of biochemical equipment and methods, enzymes, pharmaceutical formulations, etc., and can solve problems such as unsatisfactory
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0043] 《Example 1》Preparation of sea square star worm (Sipunculus nudus) plasmin star fiber N-150 protein
[0044] Put the fresh and live marine gridworm in the seafood pool and feed it with clean seawater for 24 hours to purify the impurities in its body, wash it with phosphate buffer (0.01mol / L, pH7.4), and absorb the liquid on the surface of the insect body with filter paper Finally, dissect the parasites in a cold storage at 4°C and collect the digestive glands to measure the activity, and mix with 2 times the volume of phosphate buffer (0.01mol / L, pH7.4), after homogenization by a homogenizer, set the temperature at 10000rpm at 4°C After centrifuging for 5 minutes, the supernatant was filtered through filter paper to remove fat, and the filtrate was freeze-dried by a freeze dryer. The freeze-dried product was the crude protein powder, which was the crude extract of fibrinolytic enzyme from the sea worm.
[0045] Dissolve the lyophilized powder of the crude protein extract...
Embodiment 2
[0046] "Example 2" detection of fibrinolytic activity of star fiber N-150
[0047] According to the Astrup method and the Deogny method, namely the fibrin plate method. The specific operation is as follows: Dissolve 100mg bovine fibrinogen and 100u bovine thrombin in 10ml phosphoric acid 0.01mol / L buffer solution respectively, heat and boil 80ml 0.01mol / L phosphoric acid buffer solution containing 1g agarose to dissolve, cool to At 65°C, the bovine fibrinogen solution and the bovine thrombin solution were added to the agarose solution, stirred evenly and poured into a petri dish with a diameter of 90mm, and each petri dish contained 5ml of the mixed solution. Stand at room temperature for 30 minutes to allow it to condense. Use a puncher to punch a hole with a diameter of 3mm, spot the sample to be tested on the plate, incubate at 37°C for 4h, and measure the diameter of the dissolution circle. According to this method, the observed clear and transparent area is the area whe...
Embodiment 3
[0048] "Example 3" detection of star fiber N-150 fibrinolytic protein concentration
[0049] The determination of the fibrinolytic activity of the star fiber N-150 of the present invention is calculated based on the fibrinolytic activity of a unit protein. Star fiber N-150 fibrinolytic protein concentration is determined using Micro BCA protein assay kit. Bovine serum albumin (BSA) was used as a standard for demarcating protein concentration. Under alkaline conditions, proteins will Cu 2+ reduced to Cu + , Cu + It forms a purple complex with BCA reagent, and the absorbance intensity is proportional to the protein concentration. Measure its absorbance at 562nm and compare it with the standard curve to determine the concentration of star fiber N-150 fibrinolytic protein.
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com