Tesamorelin (5MG)

$65.00

Tesamorelin is a synthetic GHRH analog widely referenced in scientific literature for studies involving endocrine signaling and peptide–receptor interactions. Researchers frequently evaluate this peptide in laboratory models focused on growth hormone regulatory pathways and molecular signaling cascades. Each vial undergoes third-party analytical testing to confirm identity and purity for laboratory research use.

Tesamorelin Peptide

Tesamorelin is a synthetic growth hormone–releasing hormone (GHRH) analog frequently referenced in scientific literature for its relevance in endocrine signaling and peptide–receptor interaction studies. Researchers commonly investigate Tesamorelin within laboratory models evaluating growth hormone regulatory pathways and hypothalamic–pituitary signaling mechanisms.

In research environments, Tesamorelin is often examined in studies exploring hormone signaling cascades, receptor-binding activity, and peptide-mediated communication systems. Its presence in peer-reviewed literature has made it a recurring compound in investigations focused on endocrine pathway mapping and molecular signaling research.

This research peptide is supplied as a lyophilized vial and undergoes third-party analytical testing to confirm identity and purity prior to distribution.


Specifications

• Peptide: Tesamorelin

• Sequence: Tyr-Ala-Asp-Ala-Ile-Phe-Thr-Asn-Ser-Tyr-Arg-Lys-Val-Leu-Ala-Gln-Leu-Ser-Ala-Arg-Lys-Leu-Leu-Gln-Asp-Ile-Met-Ser-Arg-Gln-Gln-Gly-Glu-Ser-Asn-Gln-Glu-Arg-Gly-Ala-Arg-Ala-Arg-Leu-NH2

• Form: Lyophilized Research Peptide Vial

• Purity: ≥ 98% (HPLC Verified)

• Molecular Weight: 5135.9 g/mol

• Storage: Store in a cool, dry environment away from direct light

• Intended Use: Laboratory research and analytical reference only

Certificate of Analysis

Each Hawthorne Research compound is supported by batch-specific analytical documentation verifying identity, composition, and purity through standardized laboratory testing.

Analytical Verification

  • Identity confirmation using validated analytical methods
  • Purity and chromatographic profile verification
  • Content and concentration alignment
  • Key quality parameters evaluated prior to release
  • Lot-level traceability and documentation