High-molecular polymer for stabilizing immobilized protein, and preparation method and application thereof
A complex, bovine serum albumin technology, used in analytical materials, biological testing, material inspection products, etc., can solve the problems of inability to cross-platform application, difficulty in immobilizing proteins, cumbersome steps, etc., to prevent changes in the three-dimensional structure of proteins. , Simple preparation method, simple application effect
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Embodiment 1
[0056] Example 1 Preparation of novel polymer polyethylene glycol-alkyl alcohol-bovine serum albumin-dextran (mPEG-BSA-Hexadecanol-Dextran, PBHD)
[0057] 1. Preparation of aminated dextran
[0058] The preparation flow chart is as figure 1 shown.
[0059] 1-1) Dissolve 1 g of Dextran T70 in 10 ml of acetic acid buffer solution, stir magnetically to fully dissolve, add 0.8 g of sodium periodate, protect from light, and react at room temperature for 30 min. Then add 1.1g of sodium sulfite to terminate sodium periodate, react at room temperature for 10min, then use a 10KD ultrafiltration tube for ultrafiltration, change the liquid three times with a 15mMol / L carbonic acid buffer solution with pH=9, and redissolve to a volume of 10ml for subsequent use use.
[0060] 1-2) Add 5g of lysine to 10ml of formylated dextran, stir evenly, and react at room temperature for 2 hours. Add sodium hydride to the dextran derivative, react at room temperature for 30 minutes in the dark, and ...
Embodiment 2
[0082] Embodiment 2 Preparation of a complex solution of stable immobilized protein
[0083] The complex solution of the present invention is configured as follows: Weigh 375 mg of glycine-hydrochloric acid and dissolve it in 80 ml of water, then add 0.8 g of sodium chloride, add 0.1 ml of KroVin 300, and take 5 ml of 10% polyethylene glycol-alkane prepared in Example 1 of the present invention. Add alcohol-bovine serum albumin-dextran complex (PBHD) into the solution, stir well, mix evenly, adjust the pH to 7.4 with 4N NaOH, set the volume to 100ml, and store at 4°C.
Embodiment 3
[0084] Example 3 Verification of the stability of solid-phased antibodies
[0085] Take MYO R2 latex reagent, which is reagent A, take 8ml, centrifuge at 20000g for 30min, reconstitute with 4ml of the reconstitution solution prepared in Example 2, reconstitute with 20% power ultrasonic, disperse evenly, and age at 42°C for 4h, which is For reagent B, take 8ml of MYO R2 latex reagent and directly add 0.4ml of 10% polyethylene glycol-alkyl alcohol-bovine serum albumin-dextran complex solution (prepared in Example 1), and mix evenly to obtain reagent C. Then take three R1 20ml tubes respectively, which are reagents a, b, and c, corresponding to reagents A, B, and C, and conduct an accelerated 30-day test at 37 degrees Celsius.
[0086] Use the AU680 biochemical analyzer for detection. After the reagent parameters are set, put reagents A, B, and C into the instrument for testing. The reaction process is as follows: mix the R1 reagent and the calibrator evenly, incubate at 37°C fo...
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