Tesamorelin 10mg
Tesamorelin 10mg: Potent GHRH Analogue for Metabolic Research
Tesamorelin is a synthetic analogue of Growth Hormone-Releasing Hormone (GHRH). It is modified with a hexenoyl group at its N-terminal to increase its resistance to enzymatic degradation, significantly extending its half-life compared to natural GHRH. This 44-amino acid peptide is a cornerstone in metabolic research, specifically for its highly selective ability to stimulate the pituitary gland to secrete endogenous growth hormone.
Research Highlights
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Selective GH Stimulation: Acts directly on the pituitary somatotroph cells to trigger the pulsatile release of Growth Hormone (GH) without significantly impacting other pituitary hormones.
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Visceral Adiposity Reduction: Extensively studied for its role in reducing visceral adipose tissue (VAT), the deep abdominal fat associated with metabolic dysfunction and systemic inflammation.
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IGF-1 Modulation: Research indicates that Tesamorelin effectively raises systemic Insulin-like Growth Factor 1 (IGF-1) levels, which mediates many of the anabolic and metabolic benefits of growth hormone.
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Lipid Profile Optimization: Investigated for its capacity to improve lipid metabolism, including the reduction of triglycerides and non-HDL cholesterol levels in research models.
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Cognitive & Proteomic Stability: Emerging studies explore its potential neuroprotective effects and its role in improving cognitive function by modulating GHRH signaling in the
Safety & Research Warning
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RESEARCH USE ONLY: This material is strictly for laboratory research and in vitro testing. It is not for human or veterinary consumption.
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Regulatory Status: Tesamorelin is not FDA-approved for the treatment of any disease or medical condition outside of specific clinical contexts.
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Handling: Research must be conducted in a controlled environment. Use appropriate PPE, including gloves and masks, to prevent accidental exposure.
Storage & Stability
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Lyophilized Powder: Stable at room temperature for 30 days. For long-term integrity, store at 2°C – 8°C (up to 24 months).
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Reconstituted Solution: Must be refrigerated at 2°C – 8°C. For maximum potency, utilize within 14 days of reconstitution.
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Sensitivity: Highly sensitive to heat and UV light. Avoid vigorous agitation or shaking, as the complex 44-amino acid structure is prone to mechanical denaturation.