GRADE & PURITYBioactive?Bioactive grade — verified to retain biological activity in functional assays. Use when the molecule must be functionally active, not just pure.ActiBioPure™?ActiBioPure™ — Aladdin's premier line for bioactive and recombinant products. Use when both high purity and preserved biological activity are required.Native?Native grade — protein/biomolecule in its natural (non-recombinant, non-denatured) form. Use when native structure and activity are required.High Performance?High-performance grade with optimized purity and performance characteristics. Use for sensitive analyses where ordinary grades fall short.EnzymoPure™?EnzymoPure™ — Aladdin's line of high-quality enzymatic solutions. Use when enzyme purity and defined activity drive assay or process performance.≥38000 U/mg powder
ActiBioPure™, Bioactive, High Performance, EnzymoPure™, Native, ≥38000 U/mg powder ActiBioPure™,Bioactive,High Performance,Native,EnzymoPure™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping
Room temperature,Desiccated Ships Normal Check lot-specific COA for exact specifications.
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Quality documents
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof
Cited in 7 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Descripción general
Earthworm Fibrinolytic Enzyme (Lumbrokinase) is a type of enzyme extracted and purified from earthworms that can dissolve fibrin. It is present in the digestive tract of earthworms. Earthworm Fibrinolytic Enzyme has a dual function: in addition to directly hydrolyzing fibrin, it can also activate plasminogen into plasmin, thereby exerting an indirect fibrin-hydrolyzing effect. After animals take Earthworm Fibrinolytic Enzyme, obvious antithrombotic and thrombolytic effects are produced.
Lumbokinase attenuates myocardial ischemia-reperfusion (I-R) injury through the activation of Sirt1 signaling, and thus enhances autophagic flux and reduces I-R-induced oxidative damage, inflammation and apoptosis.
Characteristics
This product is a pale yellow to yellowish-brown powder; it has a fishy odor and is hygroscopic.
Identification
Take an appropriate amount of this product, add water to prepare a solution containing 0.5mg per 1ml, and determine according to the spectrophotometry (Appendix IV A of the 2000 Edition of Pharmacopoeia of the People's Republic of China, Volume II); there shall be a maximum absorption at a wavelength of 278nm.
Take an appropriate amount of this product, add 0.9% sodium chloride solution to prepare a solution containing 10mg per 1ml as the test solution; use a No. 6 needle to take 1 drop of animal blood and place it at the bottom of a test tube. After 30 minutes, add 1ml of the test solution to the test tube, shake gently, and the blood clot shall dissolve within 60 minutes. Use 1ml of 0.9% sodium chloride solution as the blank, and perform the same operation; the blood clot shall not dissolve.
Tests
Acidity and Alkalinity: Take this product, add water to prepare a solution containing 1mg per 1ml, and determine according to the method (Appendix VI H of the 2000 Edition of Pharmacopoeia of the People's Republic of China, Volume II); the pH value shall be 6.0 - 8.0.
Clarity and Color of Solution: Take an appropriate amount of this product, add water to prepare a solution containing 1mg per 1ml; the solution shall be clear. If colored, it shall not be darker than the Yellow No. 2 Standard Color Solution (Method 1 of Appendix IX A of the 2000 Edition of Pharmacopoeia of the People's Republic of China, Volume II).
Loss on Drying: Take an appropriate amount of this product, use phosphorus pentoxide as a desiccant, dry it under reduced pressure at 60℃ to constant weight; the weight loss shall not exceed 5.0% (Appendix VIII L of the 2000 Edition of Pharmacopoeia of the People's Republic of China, Volume II).Determination of Specific Activity
Titer Determination
Reagents
0.01mol phosphate buffer (pH 7.8): Take 3.58g of disodium hydrogen phosphate, add water to dissolve and dilute to 1000ml as Solution A; take 0.78g of sodium dihydrogen phosphate (NaH₂PO₄·2H₂O), add water to dissolve and dilute to 500ml as Solution B; mix Solutions A and B until the pH value reaches 7.8.
Working Solution: Mix 0.01mol/L phosphate buffer (pH 7.8) and 0.9% sodium chloride solution at a ratio of 1:17.
1.5% Agarose Solution: Take 1.5g of agarose, add 100ml of the working solution, and heat to dissolve.
Fibrinogen Solution: Take an appropriate amount of fibrinogen, add the working solution to prepare a coagulable protein solution containing 1.5mg per 1ml.
Thrombin Solution: Take thrombin, add 0.9% sodium chloride solution to prepare a solution containing 1 BP unit per 1ml.
Preparation of Standard Solution: Take the lumbrokinase standard, add 0.9% sodium chloride solution to prepare solutions with concentrations of 10,000, 8,000, 6,000, 4,000, and 2,000 lumbrokinase units per 1ml respectively.
Preparation of Test Solution: Take an appropriate amount of this product, add 0.9% sodium chloride solution to dissolve and dilute to a concentration within the range of the standard curve.
Determination Method: Take 39ml of the fibrinogen solution, place it in a beaker, add 39ml of the 55℃ agarose solution and 3.0ml of the thrombin solution while stirring, mix immediately, and quickly pour into a plastic petri dish with a diameter of 14cm. Place it horizontally at room temperature for 1 hour, then punch holes. Precisely measure 10μl each of the lumbrokinase standard solutions of different concentrations and the test solution, spot them on the same petri dish respectively, cover the dish, and place it in a 37℃ incubator for 18 hours of reaction. After taking it out, use a caliper to measure the vertical diameters of the lysis zones. Take the logarithm of the number of units of the kinase standard as the abscissa and the logarithm of the product of the vertical diameters as the ordinate, calculate the regression equation, and substitute the logarithm of the product of the vertical diameters of the test sample into the regression equation to calculate the titer units of the test sample. Both the standard and the test sample shall be tested in duplicate, and the average value shall be used for calculation.
Protein Content
Take about 20mg of this product, weigh it accurately, determine according to the nitrogen determination method (Method 2 of Appendix VII D of the 2000 Edition of Pharmacopoeia of the People's Republic of China, Volume II), multiply the result by 6.25 to get the protein content in the test sample, and calculate the milligrams of protein per 1mg of the test sample.
Specific Activity
Calculate the specific activity according to the following formula:
Specifications
Product Name
Lumbrokinase, CAS No.556743-18-1
Grado
ActiBioPure™, Bioactive, High Performance, Native, EnzymoPure™
Especificaciones y pureza
ActiBioPure™, Bioactive, High Performance, EnzymoPure™, Native, ≥38000 U/mg powder
Bioactividad
≥38000 U/mg dry weight
CAS
556743-18-1
Tipo de molécula
Enzyme
Almacenamiento y envío
Concentración
≥38000 U/mg powder
Reconstitución
Reconstitute in 0.9% NaCl.
Condiciones de almacenamiento de almacenamiento
Room temperature,Desiccated
Enviado en
Normal
Estabilidad y almacenamiento
Store at room temperature or 2-8 ℃ long term (18 months).Upon receipt, it is recommended to aliquot. Desiccated.
Documentation
📋 Safety Data Sheet (SDS)
Comprehensive hazard, handling, storage, and regulatory compliance document.
1.Mingbo Ji, Xiangrong Chen, Jianquan Luo, Yinhua Wan. (2018) Improved blood compatibility of polysulfone membrane by anticoagulant protein immobilization. COLLOIDS AND SURFACES B-BIOINTERFACES, [PMID:30580149][10.1016/j.colsurfb.2018.12.026]
2.Yunchang Fan, Xing Dong, Yingying Zhong, Jing Li, Juan Miao, Shaofeng Hua, Yan Li, Boyu Cheng, Wenqiong Chen. (2016) Effects of ionic liquids on the hydrolysis of casein by lumbrokinase. BIOCHEMICAL ENGINEERING JOURNAL, [PMID:][10.1016/j.bej.2015.12.020]
4.Wentao Ma, Shiwen Gong, Xianbiao He, Die Hu, Bo Cheng, Jing Yang, Binbin Li, Xinyu Wang. (2025) Fucoidan-modified PLGA nanoparticles for integrated diagnosis and treatment of thrombosis. JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, [PMID:][10.1016/j.jddst.2025.107017]
5.Huang Ping, Sun Hao, Wang Yan, Wang Ning. (2025) Tong-Qiao-Huo-Xue Decoction mitigates post-stroke inflammatory response via suppression of the FIB-NLRP3 signaling pathway. METABOLIC BRAIN DISEASE, 40 (5):(1-13). [PMID:40381107][10.1007/s11011-025-01633-7]
6.Mi Xuelian, Ren Ya, Wang Hanbo, Qiang Lei, Kong Weiqing, Wang Hui, Yang Xue, Liu Yihao, Yang Han, Xiao Di, Ma Zhenjiang, Xu Guoxing, Zhang Changru, Wang Jinwu. (2025) Bioprinted integrated gradient biomechanical signal-tailored osteosarcoma model: advancing insights into tumor development and drug screening. Bio-Design and Manufacturing, 8 (3):(423-441). [PMID:][10.1631/bdm.2400108]
7.Yan Wang, Yuqin Peng, Hao Sun, Kai Zhu, Ning Wang, Changzhong Wang. (2026) Fibrinogen-Driven NLRP3 Inflammasome: A Novel Therapeutic Target for Tong-Qiao-Huo-Xue Decoction in Ischemic Stroke. Pharmaceuticals, 19 (2):(325). [PMID:41754864][10.3390/ph19020325]
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