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KPV 5 mg research vial

Melanocortin-fragment research

KPV

5 mg

Lys-Pro-Val α-MSH fragment Short-peptide signalling

A synthetic tripeptide corresponding to the Lys-Pro-Val sequence, used in controlled laboratory models of melanocortin-fragment signalling, peptide transport and short-peptide stability.

Presentation Lyophilised research material
Strength 5 mg
Use boundary Research only
Material type Synthetic tripeptide (3 amino acids)
Research focus Melanocortin-fragment signalling

£25.00

Third Party COA tested. Please contact us for reports.

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Research-use information only. Not presented for human or veterinary administration.

QUALITY ASSURANCE

Third-party COA testing

Third Party COA tested. Please contact us for reports.

ABOUT THE COMPOUND

Description & research context

KPV is the tripeptide Lys-Pro-Val, corresponding to residues 11-13 of alpha-melanocyte-stimulating hormone. Its compact sequence is used as a defined reference material in short-peptide and melanocortin-fragment research.

Published laboratory work has examined KPV transport, fragment-specific signalling and model-dependent cellular responses. Results depend on the experimental system, concentration, vehicle and analytical controls used.

APPLICATIONS IN RESEARCH

Common experimental themes

  • Melanocortin-fragment and sequence-function studies
  • Short-peptide uptake and transport models
  • Peptide stability and analytical-method development
  • Model-dependent cellular signalling research

LABORATORY HANDLING

Handling & stability

  • Handle dry lyophilised material using standard laboratory technique.
  • Select an aqueous or buffered vehicle appropriate to the assay design.
  • Avoid vigorous agitation during dissolution.
  • Use aliquots where suitable and minimise repeated freeze-thaw cycles.
  • Protect prepared material from prolonged light and elevated temperature.

RESEARCH NOTES

Interpretation & precautions

  • Observed effects depend on experimental model, concentration and exposure duration.
  • Appropriate positive and negative controls are recommended for signalling studies.
  • Reference literature is mechanistic and preclinical; observations are not clinical outcomes.
  • For laboratory research use only.

REFERENCE READING

Published and technical sources

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