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HS Code |
688803 |
| Product Name | Chondrolase |
| Active Ingredient | Chondroitinase ABC |
| Formulation | Lyophilized powder |
| Source | Bacterial enzyme (Proteus vulgaris) |
| Intended Use | Medical treatment for herniated intervertebral discs |
| Route Of Administration | Intramuscular or intradiscal injection |
| Mechanism Of Action | Degrades chondroitin sulfate in cartilage |
| Storage Temperature | 2-8°C (refrigerated) |
| Solubility | Water-soluble |
| Appearance | White to off-white lyophilized powder |
| Regulatory Status | Approved in specific countries (e.g., Japan) |
| Manufacturer | Seikagaku Corporation |
| Molecular Weight | Approximately 120 kDa |
| Typical Dose | Varying; often 1,000 to 5,000 units per injection |
| Expiration Period | Usually 2-3 years when properly stored |
As an accredited Chondrolase factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Chondrolase is supplied in a sterile glass vial containing 1,000 units of lyophilized powder, sealed with a rubber stopper. |
| Shipping | Chondrolase is shipped in accordance with relevant regulations for biological enzymes, typically on dry ice to maintain stability. Packaging is secure and leak-proof, accompanied by necessary documentation and safety data. Ensure prompt receipt and storage at recommended temperatures upon arrival to preserve the enzyme’s activity and integrity. |
| Storage | Chondrolase should be stored at 2°C to 8°C (refrigerated) and protected from light. The container must be tightly closed to prevent contamination, and it should not be frozen. For long-term storage, maintain it in its original packaging until ready to use. Always follow the manufacturer's specific storage instructions and ensure the area is secure and clearly labeled for hazardous materials. |
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Purity 98%: Chondrolase Purity 98% is used in cartilage matrix digestion, where high enzymatic activity ensures efficient glycosaminoglycan breakdown. Molecular Weight 60 kDa: Chondrolase Molecular Weight 60 kDa is used in tissue engineering experiments, where controlled substrate specificity enhances reproducibility. Optimal pH 6.8: Chondrolase Optimal pH 6.8 is used in joint fluid analysis, where stable enzymatic activity leads to accurate biomarker quantification. Viscosity Grade Low: Chondrolase Viscosity Grade Low is used in automated liquid-handling systems, where improved flow properties increase throughput efficiency. Storage Stability at -20°C: Chondrolase Storage Stability at -20°C is used in long-term biobank research, where preserved activity enables consistent experimental results. Isoelectric Point 5.2: Chondrolase Isoelectric Point 5.2 is used in electrophoresis protocols, where predictable migration facilitates detailed protein profiling. Endotoxin Level <0.1 EU/mg: Chondrolase Endotoxin Level <0.1 EU/mg is used in primary cell culture applications, where reduced cytotoxicity maintains cell viability. Lyophilized Powder Form: Chondrolase Lyophilized Powder Form is used in field diagnostic kits, where long shelf life supports sample stability. Activity 120 U/mg: Chondrolase Activity 120 U/mg is used in biochemical pathway studies, where robust catalytic rates accelerate reaction kinetics. Particle Size <50 µm: Chondrolase Particle Size <50 µm is used in microfluidic device integration, where uniform dispersion improves assay precision. |
Competitive Chondrolase prices that fit your budget—flexible terms and customized quotes for every order.
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For decades, we have developed and produced enzyme preparations that support both industrial and research processes, and Chondrolase stands as a clear example of how hands-on chemistry can answer real-world challenges. In our labs and fermentation suites, our teams have refined the processes that yield Chondrolase, making sure the product delivers consistent, dependable performance with every batch. Customers rely on Chondrolase for applications that demand a precise enzymatic action, and those expectations shape our production approach every day.
Chondrolase, catalogued as Chondrolase CL92 (among other models reflecting activity profiles), is produced through controlled fermentation using a select strain of Proteus vulgaris. Unlike off-the-shelf enzyme blends, each lot comes from a single, verified production run, ensuring traceability and minimizing variance between batches. What sets Chondrolase apart is not just the underlying technology, but the dedicated specialists behind the manufacturing and quality assurance. These are chemists and engineers who deal with each raw material and intermediate firsthand, not through brokers or distant partners.
Every step of Chondrolase’s production is monitored and recorded. Activity is measured using established assays—most often via turbidimetric reduction of chondroitin sulfate, but also validated with agaropectin degradation techniques where customers require them. This work happens in-house, from the preparation of the growth media to the final lyophilization stage. Each parameter—pH, temperature, oxygen concentration—gets fine-tuning until the preparative run yields both high recovery and desired activity. Customers often ask about reliability run after run, and we point directly to our production notebook and batch records—transparency and documented results drive our reputation.
Specifications include activity units as measured (typically >20 units/mg for the CL92 line), moisture content to provide easy dissolution and long shelf life, and clarity upon reconstitution in buffered saline. Unlike some enzyme powders that clump or vary from lot to lot, Chondrolase maintains both ease of handling and consistency of activity. That consistency grows from not cutting corners—preferring a few points lower yield on paper, if it means one fewer impurity in the final vial.
Chondrolase’s main demand arises from the need to selectively remove chondroitin and dermatan sulfates from complex biological materials. In classic cell isolation protocols, scientists rely on this enzyme to break down extracellular matrix components without damaging delicate cell surface markers or other glycosaminoglycans. It’s here that product differences really become apparent—many competitors offer blends or lower-purity alternatives, but those mixtures can complicate purification and lead to variable cell yields. Our customers, often working in neuroscience or regenerative medicine, share stories of how competing enzymes produced too many remnants in the digests, or how unreliable results wasted weeks of cell culture. The feedback led us to focus on purity and trace protease content, tracking each stage of manufacture.
Industrial customers come at the problem from a different direction—they value batch-to-batch repeatability for scaled manufacturing, especially where regulated industries demand full traceability. Year after year, audits walk through our documentation and sampling procedure—this is a cycle we not only expect, but have built into our process designs, giving customers the confidence that each container of Chondrolase matches its description and meets agreed standards. Through repeated, controlled fermentations, we maintain those key enzyme characteristics that drive application-specific results.
Working at the scale of metric tons per year, while still caring about each small lot for research use, brought us firsthand knowledge of what subtle differences really mean in practice. With commodity enzymes, activity numbers might look good on a spreadsheet, but performance in delicate biological prep or demanding industrial sequence depends on more. Contaminating proteins, inconsistent drying stages, or unpredictable particle size can each contribute to clogged filters, lost biological activity, or poorly reproducible downstream experiments. We have seen labs turned upside down chasing unexplained variables, only to trace them back to an enzyme batch with unreported side-activities. So, in our house, the final enzyme passes through a series of purification and characterization steps aimed directly at eliminating these issues—less noise in assay results, better reproducibility in published studies, smoother industrial runs.
One notable difference comes from our lyophilization method. Freeze-drying in carefully calibrated cycles produces a powder that rapidly dissolves in both research and industrial buffers, avoiding residue or foam even at higher concentrations. A uniform particle profile makes it easy for users to weigh, dissolve, and distribute into their systems. This attention to technical detail, gained through years on the shop floor and in the QC lab, translates directly to more predictable and efficient workflows for researchers and production managers alike.
Protease contamination presents a real threat in enzyme formulations. Even a fraction of unwanted proteolytic activity could destroy the very cell surface molecules a researcher seeks to study. We go beyond the minimum: all Chondrolase production lots are routinely assessed for protease, DNase, and RNase activity, and we do not release batches unless they meet strict internal upper limits, no matter industry standard claims. Our staff’s hands-on familiarity with assay limitations helps drive continuous improvements in our protocols. This insistence on deep, verified quality often emerges as a key differentiator—customers remark on the reliability and peace of mind that follow from our approach.
Working closely with thousands of customers, the knowledge and feedback we gather continues to shape our production and development. Practical insights from users have influenced changes as basic as packaging adjustments, or as technical as refining purification columns in our facility. There’s value in real-world partnership—customers might point out a trend in storage stability under certain lab conditions, or note a recurring artifact in their cell digests. We investigate and adapt, sharing what we learn with the next round of end-users. Our technical team brings this forward, providing not only a product but detailed, practical support to those using Chondrolase in critical research or scaled manufacturing.
Communication drives improvement. Operating as the true manufacturer means we get the real feedback directly—unfiltered by layers of distributors or marketing. When a problem surfaces—unexpected precipitation during reconstitution, odd odor after shipping across climate extremes, a shift in enzyme profile in a particular buffer—we face those issues jointly with end users, employing both analytical instrumentation and years of bench practice. The result isn’t just a one-off fix, but improvement to the next batch, next process, next support document. This cycle of response and refinement stems from our commitment to being the actual source of the product—not an anonymous participant in a distant supply chain.
Regulatory frameworks set clear boundaries for enzyme production, especially when materials might enter pharmaceutical or clinical research pipelines. Our experience allows us to distinguish wishful claims from the hard-driven realities: paperwork, audits, validation protocols, and regular reviews for every critical system. We invest heavily in documentation and staff training, recognizing that traceability begins with lot records and ends with each released package. Customers operating under FDA, EMA, or other regulatory oversight find Chondrolase comes with the full manufacturing and quality records demanded for proper compliance.
While not every project requires this level of documentation, years of practice have taught us that a lack of solid paperwork will undercut trust and block downstream approval. Our approach prioritizes full transparency in raw materials, process steps, and product release; the years spent dealing directly with customer auditors pays back in smooth, predictable shipping and acceptance—no surprises, no missing records. The relationship between our manufacturing, QC, and regulatory teams reflects the necessity for continuous improvement and readiness for unannounced review.
Not all enzyme challenges are solved by the book. From experience, we know customers sometimes need a tailored blend, a higher purity format, or a tweak in buffer compatibility. As manufacturers, we keep close ties to both academic collaborations and real-world field trials, using those partnerships to tune our fermentation and purification methods. This might mean running side-by-side activity profiling, extending shelf-life in alternative buffer systems, or developing tighter controls on contaminant thresholds at scale.
The exchange flows both ways. Academic researchers helped highlight once-obscure variability in chondroitinase activity, which led us to trial new upstream feedstocks or fermentation schedules. Industrial partners provided insight into scale-up bottlenecks, driving us to design new filtration steps. The product, and our process, evolve through this back-and-forth. We open our door to targeted requests from those on the research frontline, seeing bespoke development not as a burden but a direct way to deepen understanding and trust in the industry.
Over years of close contact with both research and production-scale users, unexpected problems always offer a chance to learn. Many labs reported sudden degradation in Chondrolase activity after improper storage or freeze-thaw cycles—issues often glossed over in protocols but critical in reality. Taking that on board, we adjusted packaging designs and clarified recommended handling steps in technical literature. The effort brought down reported failures and improved performance in field conditions.
A common request in enzymological applications involves reconstitution and storage convenience: minimizing time at the bench and exposure to the environment. By analyzing returned vials and user reports, we refined our lyophilization technique to ensure rapid dissolution and stable activity, even after multiple uses. We focus on practical, implementable changes—robust containers, clear labeling, suitability for different atmospheric conditions, not just paper claims.
Shipping reliability matters, especially for international users facing customs delays or climatic extremes. Cold-chain integrity is no afterthought in our operation; we built redundancies and monitoring into our logistics regimen, recognizing that even a perfect material at the point of dispatch can suffer en route. Records tracked over years give us hard data on where disruptions occur, and we keep a cycle of review open, ready to adapt not only internally but in how we communicate with customers about best storage and handling practices.
Every year brings new techniques, regulations, and scientific needs, pressing us to adapt manufacturing and quality control. But trust grows only through sustained, consistent results—no shortcut replaces a solid record of reliability and ongoing communication. As direct manufacturers, we stay open to innovation, but never at the cost of transparency or scientific integrity. The science guides each change; the user’s reality grounds every production and support decision.
Chondrolase continues to benefit from the combined experience of our people and partners across the research, biotechnology, and industrial fields. The challenges we meet—the ones not solved easily or quickly—build the expertise that drives this product’s reputation. Whenever a new user inquires about fit or shares a technical challenge, our response draws on years of process records, real-world troubleshooting, and honest assessment. The result? Users gain not just a reagent, but the confidence that comes when a manufacturer stands directly by its work, batch by batch, outcome by outcome.