Cobra-venom factor and cobra-venom neurotoxin combined separation and purification method
A technology of cobra venom factor and cobra venom, which is applied in the field of biomedicine, can solve problems such as unsuitable for large-scale production process, ineffective utilization of snake venom protein, and easy compression of chromatographic columns, so as to reduce mutual interference, avoid protein denaturation, The effect of high comprehensive utilization
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[0032] In an embodiment, a combined separation and purification method of cobra venom factor and cobra venom neurotoxin adopts the following steps:
[0033] 1. Handling of sample crude virus
[0034] Weigh 20g of snake venom and dissolve it in 200ml of purified water or Tris buffer of pH5-8, centrifuge at 10000rpm at a temperature below 10°C for 10min, take the supernatant, and pass through a 0.22μm microporous membrane. The 5kDa ultrafiltration membrane is exchanged for the separation buffer;
[0035] 2. CM-Sepharose FF chromatography
[0036] The snake venom solution after the exchange buffer is loaded onto the CM Sepharose FF chromatographic column (5.0 × 30cm) equilibrated with Tris buffer solution of pH 7.5 and 20mmol / L with a peristaltic pump at a flow rate of 10ml / min, and eluted with the equilibrium buffer After the flow-through peak is collected, NaCl is added to the elution buffer to elute separately. The concentration of NaCl added is 0.1M, 0.2M, and 0.4M. The flo...
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