Marine Brightening Factor MEGPEP TXOD originates from symbiotic marine yeast inhabiting red coral communities, engineered via cDNA library reconstruction and homologous recombination to deliver high-purity oxidoreductase sequences through fermentation.
It features dual active domains: a copper-containing superoxide dismutase oxidoreductase and a highly conserved thioredoxin catalytic center, effectively neutralizing reactive oxygen species (ROS) and lipid peroxides. Verified through zebrafish in vivo testing, it diminishes melanin signals, clarifies dull yellow tones, and restores luminous, even-toned skin.
Marine Microbial Fermentation
Coral-symbiotic marine yeast culture and natural redox enzyme system.
RAW MATERIAL TECHNICAL & REGULATORY DOSSIER
Comprehensive Technical, Quality Specification, and Regulatory Dossier for R&D Formulators, Procurement, and Product Managers
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Biotechnology Mechanism & Scientific Evidence
Authoritative Brochure Technical Diagram · Molecular Model · Transdermal & Efficacy Mechanism
Mechanism DiagramMarine microbial antioxidant redox enzyme TXOD in zebrafish model: melanin reduction and photoaging protection.
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Formulation R&D Engineer Guide (R&D Technical Dossier)
Formulation Application · Physicochemical Parameters · Stability & Compatibility
| INCI Name (CN) |
Oxidoreductase酶、甘氨酸、精氨酸、聚山梨醇酯-20、1,2-1,2-Hexanediol, Aqua |
INCI Name (EN) |
Aqua, Fibronectin, Alteromonas Ferment Extract, Glycerin, 1,2-Hexanediol |
| CAS No. |
9001-73-4 / 56-40-6 / 74-79-3 / 9005-64-5 / 6920-22-5 / 7732-18-5 |
Recommended Dosage |
0.5% - 5.0%（Brightening 1.0% - 2.0%） |
| Optimal pH Range |
5.5 - 7.0 |
Thermal Processing |
Add below 45°C during the cooling phase |
| Appearance & Odor |
Light amber transparent liquid, mild oceanic aroma |
Solubility & Method |
Easily miscible with aqueous phase |
💡 Compatibility Guidelines & Precautions: Compatible with vitamin C derivatives, niacinamide, and arbutin
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Procurement & Compliance Dossier (Procurement & Compliance)
NMPA Code · MOQ · Sampling Support · Certificate of Analysis
| NMPA Submission Code |
✓ 183724-00075-3281 |
Supply Packaging |
1kg/fluorinated bottle, 5kg/drum, 25kg/drum |
| Minimum Order Quantity (MOQ) |
1 kg (Ready Stock) |
Delivery Lead Time |
Dispatched within 24-48 hours |
| Storage Conditions |
Store in a cool, dry place at 2-8°C, protected from light |
Shelf Life (Shelf Life) |
24 Months |
| R&D Sample Support |
Complimentary 30g trial sample available with whitening test data |
Quality Documentation |
Batch COA, SDS, TDS, Tyrosinase Inhibition Assay Report |
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Product Planning & Marketing Highlights (Marketing Highlights)
Core Mechanism · Efficacy Claims · Recommended Formats · Scientific Backing
🧬 Core Bio-Tech Barrier & Mechanism of Action:
Deep-sea microorganism-derived transdermal fibronectin anchors epidermal repair and reduces dull pigmentation to brighten and even skin tone.
✨ Key Selling Point Keywords:
🏷️ Multi-Pathway Tone Improvement🏷️ Mitigating Pigment Accumulation🏷️ Relieving Dull & Sallow Skin Tone🏷️ Gentle & Non-Irritating🏷️ Even-Toned & Luminous Radiance
🧴 Recommended Product Formats & Categories:
Brightening treatment serums, spot correcting creams, radiant glow sheet masks, illuminating toners
📜 Patented Technologies & Scientific Backing:
Deep-Sea Extreme Microbe Fermentation & Metabolite Fractionation Patent
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Regulatory Compliance & Peer-to-Peer Disclaimer
Regulatory & Professional Compliance Statement:
1. The raw material characteristics and experimental data (including cytological studies, mechanism diagrams, and literature citations) presented on this webpage are intended exclusively for technical discussion and formulation R&D reference by cosmetic brand formulators, R&D engineers, product planners, and academic research institutions. They do not constitute finished consumer cosmetic efficacy claims or commercial warranties.
2. Pursuant to the Regulations on the Supervision and Administration of Cosmetics, Standards for Cosmetic Efficacy Claim Evaluation, and relevant global cosmetic regulatory frameworks, cosmetic brand enterprises utilizing this raw material shall be solely responsible for the safety, stability, and efficacy claims of their finished consumer products, and shall independently complete efficacy evaluations and regulatory filings/registrations with the competent health authorities prior to commercial launch. Conclusions from in-vitro or cellular studies shall not be directly extrapolated as consumer claims.
3. Mellgen Biotech assumes no joint or indirect liability for any claims or regulatory non-compliance arising from improper customer formulation, unauthorized off-label claims, or unverified applications.
