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  • MELLPRO MAP Recombinant Mussel Adhesive Protein
Sample Pack Specification: 30g/50g R&D Testing Sample (Global Courier Support)
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MELLPRO MAP Recombinant Mussel Adhesive Protein

Cosmetic Raw Materials

Genetically engineered humanized mussel adhesive protein (MAP) rich in specific DOPA groups, providing super-strong wet surface adhesion, breathable barrier film formation, and instantaneous soothing of redness and sensitive irritation.

INCI Name: Aqua, Recombinant Mussel Adhesive Protein, Glycerin, 1,2-Hexanediol

Appearance & Solubility: Colorless to pale straw clear liquid, Readily soluble in water phase

Recommended Dosage: 0.5% - 3.0% (Recommended 1.0% - 2.0%)

Online Inquiry

Hotline: 136-9197-8530

Genetically engineered humanized mussel adhesive protein (MAP) rich in specific DOPA groups, providing super-strong wet surface adhesion, breathable barrier film formation, and instantaneous soothing of redness and sensitive irritation.

MELLPRO MAP Recombinant Mussel Adhesive Protein - Mechanism & Scientific Evidence

Scientific Illustration MELLPRO MAP Recombinant Mussel Adhesive Protein - Mechanism & Scientific Evidence

RAW MATERIAL TECHNICAL & REGULATORY DOSSIER

Comprehensive Technical, Quality Specification, and Regulatory Dossier for R&D Formulators, Procurement, and Product Managers

📊 Biotechnology Mechanism & Scientific Evidence
Authoritative Brochure Technical Diagram · Molecular Model · Transdermal & Efficacy Mechanism
MELLPRO MAP Recombinant Mussel Adhesive Protein - Mechanism of Action and Transdermal Delivery Pathway

Mechanism DiagramMELLPRO MAP Recombinant Mussel Adhesive Protein - Mechanism of Action and Transdermal Delivery Pathway

🔬 Formulation R&D Engineer Guide (R&D Technical Dossier)
Formulation Application · Physicochemical Parameters · Stability & Compatibility
Standard INCI Name Aqua, Recombinant Mussel Adhesive Protein, Glycerin, 1,2-Hexanediol CAS Registry No. 103125-93-7 / 7732-18-5
Recommended Dosage 0.5% - 3.0% (Recommended 1.0% - 2.0%) Optimal pH Range 5.0 - 6.5
Thermal Processing Add below 40°C during final formulation phase Solubility & Method Readily soluble in water phase
Appearance & Odor Colorless to pale straw clear liquid Patented Tech / IP Recombinant Mussel Adhesive Protein (Purity >98%)
💡 Compatibility Guidelines & Precautions: Avoid strong alkaline conditions (pH >7.5) to prevent DOPA auto-oxidation
📦 Procurement & Compliance Dossier
NMPA Code · MOQ · Sampling Support · Certificate of Analysis
NMPA Submission Code ✓ 008671-03099-2205 Supply Packaging 1kg/fluorinated bottle, 5kg/drum, 20kg/drum
Minimum Order Quantity (MOQ) 1 kg (Ready Stock) Delivery Lead Time Dispatched within 24-48 hours
Storage Conditions Store refrigerated at 2-8°C, protected from light Shelf Life 24 Months
R&D Sample Support Complimentary 30g trial sample with application protocols Quality Documentation Batch COA, SDS, TDS, Wet Surface Adhesion & Safety Reports
💡 Product Planning & Marketing Highlights
Core Mechanism · Key Selling Points · Recommended Formats · Scientific Backing
🧬 Core Bio-Tech Barrier & Mechanism of Action:

DOPA moieties undergo rapid coacervation on moist skin surfaces, creating a microscopic, flexible, bio-adhesive protective mesh that shields nerve endings, accelerates re-epithelialization, and quenches inflammatory cascades.

🧴 Recommended Product Formats & Categories:

Medical aesthetic post-laser dressings, redness relief sprays, sensitive barrier rescue serums, anti-itch creams

📜 Patented Technologies & Scientific Backing:

Granted Invention Patent on Recombinant Mussel Adhesive Protein Synthesis

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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.

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