High Purity Tirzepatide GLP-GIP Dual Target Freeze-Dried Lab Research Solid Reagent

  Product Detail  

Brief Overview

Core Research Application & Functional Features

1. Permitted Research Scope Only

• In-vitro dual GLP-1 & GIP receptor binding affinity cell culture tests
• Type 2 glucose homeostasis disorder and insulin sensitivity mechanism comparative trials
• Gastric emptying signal and appetite regulation pathway observation experiments
• Visceral fat accumulation, lipid breakdown and energy expenditure quantitative detection research
• Cardiomyocyte metabolic protection and oxidative stress balance academic biochemical projects
• Concentration gradient contrast experiments on dual hormone signal cascade inside cell models
• Long-cycle metabolic stability and albumin binding duration comparative lab research with single-target signal solids

2. Unique Research Advantages

1. Dual Receptor Specific Binding Performance
   
   
   The molecular structure can simultaneously stably bind to both GLP-1 and GIP cell surface signal receptors, activate two independent downstream metabolic signal pathways inside test carriers. It provides single-variable clear comparative data for dual-incretin signal transduction related lab tests, avoiding multi-factor interference to experimental results, which cannot be achieved by single-target research solids.
2. Superior Freeze-Dried Long-Term Activity Stability
   
   
   Low-temperature vacuum dehydration locks complete full molecular frame with intact fatty acid side chain modification without structural dissociation during storage and transportation. It effectively solves the activity attenuation defect of liquid medium samples, greatly reducing frequent re-preparation workload for long-period lab inventory management and long-cycle animal model trials.
3. Wide Compatibility With Standard Cell Culture Systems
   
   
   This solid can fully blend with lab bacteriostatic purified water and PBS buffer liquid, compatible with most conventional mammalian pancreatic cell, adipocyte, cardiomyocyte and tissue slice test systems, without introducing extra interfering impurities to cell culture environment.
4. Distinct Concentration Gradient Experimental Response
   
   
   Adjustable working concentration fits diversified lab design; glucose regulation, lipid metabolism and antioxidant indicators show regular gradient changes under different addition dosages, convenient for quantitative data statistics and academic paper result analysis of dual-hormone contrast studies.
5. Ultra-Low Impurity Interference Profile
   
   
   Multi-stage precise purification workflow minimizes irrelevant truncated molecular fragments, oxidation residues and incomplete modified by-products inside finished solid. It will not generate extra noise signals in spectrophotometry and fluorescence detection equipment, ensuring high-definition output of quantitative biochemical binding test data.
6. Uniform Batch-to-Batch Consistency
   
   
   Standardized full synthesis, purification and freeze-drying production workflow ensures identical purity, dissolving performance and dual-receptor binding signal activity across all production lots. No test result deviation caused by inconsistent raw material quality, fully fit for parallel comparison experiments and repeated result verification of dual-target control groups.

Complete Standard Specification Parameters

Basic Product Identification Info

• Full Product Name: Tirzepatide GLP-GIP Dual Hormone Signal Molecular Solid
• Alias: Dual Incretin Target Metabolic Research Reagent
• CAS Reference Number: 2023788-19-2
• Molecular Formula: C₂₂₅H₃₄₈N₄₈O₆₈
• Theoretical Molecular Weight: 4813.45 Da
• Visual Form: Uniform white freeze-dried solid, free of clumps, discoloration, tiny foreign particles or visible impurities
• Odor Characteristic: Completely odorless
• Dissolving Performance: Fully blendable with lab bacteriostatic purified water and PBS buffer liquid; cannot mix with alcohol-based lab liquid medium
• Post-dissolving Liquid State: Clear colorless transparent solution without suspended particles, turbidity or precipitate after full dissolution
• pH Value of 1mg/mL Mixed Liquid: 4.6 ~ 6.5
• Residual Moisture Content Test Index: ≤ 2.0% (tested via Karl Fischer titration method per batch)
• Endotoxin Level: < 0.1 EU/mg, fully comply with global universal safety standards for cell and animal lab research
• Heavy Element Residue Control Limit: Lead ≤10ppm, Arsenic ≤2ppm, Cadmium ≤1ppm, Mercury ≤1ppm
• Microbe Control Standard: Total aerobic microbes <10 CFU/mg, yeast and mold <5 CFU/mg; zero harmful pathogenic bacteria detected in all batches
• Molecular Frame Integrity: Spectrum matching test carried out for every batch to confirm complete intact full molecular frame and intact fatty acid side chain modification without breakage or incomplete conjugation

Available Sealed Vial Sizes (No bulk kilogram supply)

• TIR-05: 5mg freeze-dried dual hormone signal solid per vacuum-sealed neutral glass vial
• TIR-10: 10mg freeze-dried dual hormone signal solid per vacuum-sealed neutral glass vial
• TIR-15: 15mg freeze-dried dual hormone signal solid per vacuum-sealed neutral glass vial

Strict Production & Inspection Quality Control Standards

1. Core High Purity Benchmark
   
   
   Guaranteed HPLC chromatographic purity of finished dual hormone signal solid ≥99.0%. Complete spectrum chromatogram records are attached to each batch test report. Single unknown individual impurity ≤ 0.3%, total combined unknown impurities ≤ 1.0%. Testing adopts C18 reverse-phase chromatographic column with 220nm UV wavelength detection for precise purity numerical measurement, separately verifying complete fatty acid side chain modification integrity.
2. Mandatory Full Batch Testing Items

• Spectrum molecular weight matching test, ensuring measured molecular weight error within ±5 Da compared with theoretical standard value
• Full molecular frame and modification site structural verification to confirm complete matching with standard Tirzepatide molecular configuration
• Trace residual substance testing following ICH Q3C standardized limits
• Constant temperature & humidity accelerated stability test for shelf life validity validation
• Dual GLP-1 & GIP receptor binding biological activity detection to lock stable and consistent lab research performance
• 100% manual visual full inspection of all finished sealed vials before shipment to screen out defective goods
• Complete batch full traceability management system covering raw material incoming records, production operation logs, full-item inspection data and outgoing delivery archive files

Standard Step-by-Step Dissolving Operation Guidance

Recommended Matching Liquid Medium: Lab dedicated bacteriostatic purified water

1. Slowly pour bacteriostatic purified water along the inner wall of the glass vial to avoid massive foaming generation
2. Fully tighten the vial cap, rotate and swirl gently in circular motion until all freeze-dried solid material dissolves completely
3. Do not shake the vial violently; fierce agitation will break complete molecular frame and fatty acid side chain structure, weaken stable dual-receptor binding signal activity

Storage Environment & Valid Usage Period Rules

Unopened Original Vacuum-Sealed Vials

• Long-term storage environmental condition: Keep fully sealed vials stored at -20°C ~ -80°C, completely shielded from direct light and high moisture
• Valid storage duration under constant -20°C freezing environment: 12 months
• Valid storage duration under constant -80°C ultra-low temperature environment: 36 months
• Short transit stability tolerance: Maintain stable dual-receptor binding signal activity for up to 7 days under ambient temperature below 25°C
• Forbidden storage behavior: Frequent repeated temperature fluctuation, long-time direct sunlight exposure

Liquid Mixed With Bacteriostatic Purified Water

• Storage condition after dissolution: Place inside refrigerator under 2°C ~ 8°C refrigeration environment, fully shaded
• Suggested full usage time limit: Consume all mixed liquid within 14 days after preparation completion
• Strict prohibition: Do not freeze diluted mixed liquid; repeated freezing and thawing cycles will permanently damage molecular frame and fatty acid modification stability, lose dual-target research signal activity

Shipping & Receiving Handling Reminders

1. Small trial vial orders can be delivered via standard international express for short-distance cross-border transit
2. Large quantity multi-vial orders are strongly suggested to choose temperature-insulated protective packaging to maintain stable molecular state during long-distance overseas transportation
3. Complete supporting shipping documents will be delivered together with all parcels, including unified technical data sheets and batch exclusive test records for customs inspection and internal lab filing use

Lab Operation Safety Reminders

1. Wear disposable nitrile protective gloves, transparent safety goggles and dust-proof lab masks during powder weighing and dissolving operating procedures
2. Avoid direct skin contact, eye contact and inhalation of dry freeze-dried dual hormone signal solid powder
3. In case of accidental contact with skin or eye tissue, flush the affected area thoroughly with plenty of clean running water immediately
4. Dispose of residual solid powder and waste mixed liquid strictly following internal waste management rules of your laboratory; do not pour residual liquid directly into domestic drainage pipelines or general household waste bins

Important Usage Restriction Statement

Free Supporting Technical Documents Provided For All Orders

1. Batch exclusive test report with full HPLC spectrum purity test data records
2. Full-version unified technical data sheet covering all specifications, dissolving operation steps and standard storage rules
3. Complete molecular structure schematic diagram and structural modification verification file
4. Full inspection records of heavy element, endotoxin and microbe testing indexes
5. Original raw data of long-term molecular stability accelerated testing