Tesamorelin 10MG

$55.00

GHRH analog studied for GH/IGF-1 axis and visceral adipose research

10 in stock

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SKU: AT-TESA-10 Category:

Research Materials · COA Available · Ships From USA

Tesamorelin 10MG$55.00

Overview

Tesamorelin is a synthetic analog of growth hormone-releasing hormone (GHRH). It consists of the full 44-amino acid sequence of endogenous GHRH with a trans-3-hexenoic acid modification at the N-terminus that increases plasma stability by reducing enzymatic degradation via dipeptidyl peptidase IV (DPP-IV). This modification extends the compound half-life compared to native GHRH without altering receptor binding characteristics. Tesamorelin has been extensively studied in preclinical research, providing a broad published literature base for researchers.

Alpha Tides PNW supplies Tesamorelin as a 10mg lyophilized compound for laboratory research use. For the tested sample, the attached Janoshik Certificate of Analysis reports 99.015% purity.

Research Applications

  • GH/IGF-1 axis modulation: Pituitary growth hormone release and downstream IGF-1 pathway activation studies
  • Visceral adiposity research: Adipose tissue reduction mechanisms and lipid metabolism studies
  • Cognitive research models: Studies examining GH/IGF-1 axis activity and hippocampal function in aging research models
  • Lipodystrophy models: Metabolic consequence and reversal research in preclinical lipodystrophy study designs
  • Pituitary function studies: GHRH receptor pharmacology and somatotroph response characterization
  • GHRH analog pharmacology: Plasma stability comparison studies between native GHRH and modified analogs

Research Notes

Tesamorelin acts on hypothalamic GHRH receptors (GHRHR) on pituitary somatotrophs, triggering cAMP-mediated GH synthesis and pulsatile secretion. Its trans-3-hexenoic acid N-terminal modification protects against DPP-IV degradation — the primary enzymatic pathway responsible for GHRH inactivation — thereby extending plasma half-life relative to endogenous GHRH.

A significant area of preclinical research on Tesamorelin involves visceral fat reduction and lipid metabolism, an active focus of body-composition and metabolic research. Research has also examined its role in cognitive research models relevant to GH/IGF-1 axis activity in aging, an area of ongoing investigation.

An attached Certificate of Analysis from Janoshik Analytical is available for this product.

Storage Notes

  • Before reconstitution: Store lyophilized vials at −20°C, protected from light and moisture. Allow to reach room temperature before opening.
  • After reconstitution: Refrigerate at 2–8°C and use within 28 days. Avoid repeated freeze-thaw cycles.
  • Recommended solvent: Bacteriostatic water for most research protocols.

Related Research

Tesamorelin is intended strictly for laboratory research by qualified professionals. It is not FDA approved for general use and is not for human or animal administration. By purchasing, the buyer confirms the product will be used solely for in vitro research in compliance with all applicable laws and regulations.

Product NameTesamorelin 10MG
Research CategoryGH Secretagogue Research
FormLyophilized powder
Quantity10mg per vial
Purity99.015% reported for the tested sample in the attached Janoshik Certificate of Analysis
Storage−20°C lyophilized; 2–8°C after reconstitution
COA AvailableYes
Batch TestedYes — verified by independent lab
Research Use OnlyFor laboratory and in vitro research use only
ShippingFree Standard Shipping Included

Research Accessories

Frequently Asked Questions

Both are GHRH analogs but with different structural modifications. Tesamorelin uses a trans-3-hexenoic acid modification for DPP-IV protection and retains the full 44-amino acid GHRH sequence. CJC-1295 typically uses a drug affinity complex (DAC) modification for albumin binding, extending half-life further and producing a more sustained GH release pattern. The two are sometimes compared in GHRH receptor pharmacology studies examining GH pulse kinetics.

Tesamorelin has an established preclinical and pharmacological research literature examining its GHRH receptor activity, visceral fat and lipid metabolism effects, and cognitive research applications in aging models. It remains an active reference compound in GH/IGF-1 axis research.

Store lyophilized vials at −20°C before reconstitution. After reconstitution with bacteriostatic water, refrigerate at 2–8°C and use within 28 days.