Snake venom protein component of ahylysantinfarctase at southern Anhui Province, extraction method and uses thereof
A technology of snake venom protein and Viper, which is applied to the components, extraction and application fields of Viper venom in southern Anhui, and can solve the problem of masking the anticoagulant activity of anticoagulant components, being less discovered, and mixing thrombin-like substances. problem, to achieve the effect of anti-tumor immune system function and improve immune system function
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Embodiment 1
[0033] The venom of Agkistrodon acutus in southern Anhui was purchased from Jinzhong Snake Farm in Ningguo City, Anhui Province.
[0034] CXG-1 column chromatography cabinet: contains TH-1000 gradient mixer, DHL-A computer constant flow pump, HD-5 computer ultraviolet detector, DBS-100 computer automatic partial collector (Shanghai Huxi Analytical Instruments) factory limited)
[0035] DEAE Sepharose Fast Flow gel, SP Sepharose Fast Flow gel, SephadexG75 gel are all produced by Swedish Pharmacia Company.
[0036] The BCA method protein content detection kit was produced by PIERCE Company of the United States.
[0037] a) Anion chromatography step: dissolve 1 gram of Agkistrodon acutina venom crude poison in 0.01mol / LTris-Hcl solution of pH 8.0, centrifuge at 6000rpm, take 200ml DEAE agarose gel FF column on 10ml of supernatant, use 0.01mol / L Tris-Hcl solution with pH8.0 and 0.01mol / L Tris-Hcl solution with pH8.0 containing 0.5mol / L NaCl for gradient elution, the temperature ...
Embodiment 2
[0050] a) Anion chromatography step: Dissolve 1.2 grams of the crude venom of Agkistrodon venom in 0.008mol / LTris-Hcl solution with pH 7.8, centrifuge at 5000rpm, take about 10ml of the supernatant and put it on a 220ml DEAE Sepharose FF column, Use 0.008mol / L Tris-Hcl solution with pH 7.8 and 0.008mol / L Tris-Hcl solution containing 0.45mol / L NaCl for gradient elution, the temperature is 0℃~10℃, the flow rate is 0.4ml / min, and the collection time is 20min One tube, use a UV detector to detect at 280nm, record the chromatogram, collect the eluent from each peak according to the spectrum, measure the anticoagulant activity of each peak by APTT method, select the peak with the most obvious prolongation of anticoagulant time, and collect this peak The eluate from each tube was put into a dialysis bag, desalted and concentrated to obtain snake venom 1;
[0051] b) Cationic chromatography step: Centrifuge 12ml of snake venom at 5000rpm, take 2ml of the supernatant and put it on a 20...
Embodiment 3
[0054]a) Anion chromatography step: dissolve 0.9 grams of the crude poison of Agkistrodon venom in the 0.012mol / LTris-Hcl solution of pH 8.1, centrifuge at 6500rpm, take 10ml of the supernatant and put it on a 180ml DEAE Sepharose FF column, use 0.012 mol / L Tris-Hcl solution with pH 8.1 and 0.012 mol / L Tris-Hcl solution containing 0.55 mol / L NaCl were used for gradient elution, the temperature was 0°C-10°C, the flow rate was 0.6ml / min, and a sample was collected in 20 minutes. Use a UV detector to detect at 280nm, record the chromatogram, collect the eluent from each peak according to the spectrum, measure the anticoagulant activity of each peak with the APTT method, select the peak with the most obvious prolongation of anticoagulant time, and collect the peaks for each peak. tube eluent, put into dialysis bag, desalted and concentrated to obtain snake venom 1;
[0055] b) Cationic chromatography step: Centrifuge about 3ml of snake venom 1 at 6500rpm, take 3ml of the supernata...
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