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Item: KISSPEPTIN·Reference Standard

Kisspeptin

From $31.50to $262.50

Kisspeptin-10 peptide (human), lyophilized reference standard for in vitro laboratory research.

KISSPEPTIN 10 mg research compound vial from KAM Research
KISSPEPTIN
10 mg
Pack
Strength
VOLUME TIER20% Quantity Tier (20% total savings)
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Price (/ pack)

$140.00

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5 total vials

$140.00

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Single Vial List Price:$35.00 / vial
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Certificate of Analysis & Specifications

Documentation will be published once this lot completes third-party analytical release.

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Research Data

Chemical & Structural Identifiers

Chemical Name (IUPAC)
L-tyrosyl-L-asparaginyl-L-tryptophyl-L-asparaginyl-L-seryl-L-phenylalanylglycyl-L-leucyl-L-arginyl-L-phenylalaninamide
CAS Registry Number
374675-21-5 (Kisspeptin-10 monomer)
PubChem CID
9832791
Molecular Formula
C63H83N17O14
Molecular Weight
1301.63 Da (1302.44 g/mol average)
Sequence
H-Tyr-Asn-Trp-Asn-Ser-Phe-Gly-Leu-Arg-Phe-NH2 (Single-letter: YNWNSFGLRF-NH2)
SMILES
CC(C)C[C@@H](C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N)NC(=O)CNC(=O)[C@H](CC2=CC=CC=C2)NC(=O)[C@H](CO)NC(=O)[C@H](CC(=O)N)NC(=O)[C@H](CC3=CNC4=CC=CC=C43)NC(=O)[C@H](CC(=O)N)NC(=O)[C@H](CC5=CC=C(C=C5)O)N
InChIKey
KKLNQVYXQYYYPA-XVBWMSOYSA-N
Salt / Counter-Ion
Supplied as a high-purity lyophilized acetate (CH3COO-) or trifluoroacetate (CF3COO-) salt.
Synonyms
Kisspeptin-10, KP-10, Metastin (45-54), KISS-1 (112-121), Kp10 Decapeptide

Analytical & COA Specifications

Analytical Purity (RP-HPLC)
≥ 98.0% area normalization under UV detection at λ = 214 nm and 280 nm (tyrosine and tryptophan chromophore detection).
Identity Confirmation (RP-HPLC RT + UV vs. reference)
Main peak retention time and UV spectrum conform to the reference standard.
Physical Characterization
Dense, white to off-white lyophilized solid cake/powder.

Handling & Stability

Storage. Store dry solid desiccated at -20°C to -80°C, sealed under an inert gas matrix and protected from ambient light.

Solubility. Soluble in sterile laboratory-grade deionized water (≥ 10 mg/mL), sterile Phosphate-Buffered Saline (PBS, pH 7.4, ≥ 5 mg/mL), or dilute sterile 0.1% acetic acid for stock stabilization in in vitro assay applications.

  • Photostability & Handling Parameters: Contains aromatic residues (Tyr1, Trp3, Phe6, Phe10) that exhibit UV sensitivity; prepare concentrated stock solutions under amber light conditions, avoid high-shear vortexing, and aliquot into single-use fractions at -20°C to eliminate degradation from repeated freeze-thaw cycles.

Mechanism & Literature

Endogenous RF-amide neurohormone decapeptide serving as the minimum active pharmacophore of the KISS1 gene products. Functions as a full, high-affinity agonist at the G-protein coupled Kisspeptin Receptor (KISS1R / GPR54 / AXOR12), exhibiting nanomolar affinity (Ki ≈ 1.5--4.5 nM).

Cellular Pathways Investigated: Extensively documented in in vitro hypothalamic cell models (e.g., GT1-7 GnRH neuronal cell lines) and receptor-transfected cultures (CHO-K1/HEK293 expressing GPR54) to evaluate Gαq/11 signal transduction, Phospholipase C (PLC) activation, inositol 1,4,5-trisphosphate (IP3) and diacylglycerol (DAG) turnover, transient intracellular calcium mobilization ([Ca2+]i), and downstream phosphorylation of Extracellular Signal-Regulated Kinase 1/2 (pERK1/2) that triggers gonadotropin-releasing hormone (GnRH) gene transcription.

References (3)
  1. Kotani, M., et al. (2001). The metastasis suppressor gene KISS-1 encodes kisspeptins, the natural ligands of the orphan G protein-coupled receptor GPR54. Journal of Biological Chemistry, 276(37), 34631–34636.
  2. Seminara, S. B., et al. (2003). The GPR54 gene as a regulator of puberty and hypothalamic signaling in cellular and animal models. New England Journal of Medicine, 349(17), 1614–1627.
  3. Roseweir, A. K., et al. (2009). Discovery of potent kisspeptin antagonists delineate the role of KISS1R in gonadotropin release in vitro. Journal of Neuroscience, 29(12), 3920–3929.

Technical Laboratory FAQs

What structural element is essential for Kisspeptin-10 biological activity in vitro?

The C-terminal amidation (Phe10-NH2) and conserved C-terminal RF-amide motif (Arg9-Phe10-NH2) are critical for binding into the hydrophobic pocket of the KISS1R (GPR54) receptor; deamidation to free carboxyl forms drastically impairs receptor affinity in cell assays.

How does Kisspeptin-10 compare functionally to full-length Kisspeptin-54 in receptor binding assays?

Kisspeptin-10 represents the truncated C-terminal 10-amino-acid domain of Kisspeptin-54 and demonstrates equivalent binding affinity (Kd) and functional potency (EC50) in stimulating IP3 turnover and intracellular calcium influx in GPR54-expressing cell lines.

What solvent conditions are recommended for preparing in vitro Kisspeptin-10 working stocks?

Sterile deionized water or sterile PBS (pH 7.4) is standard for baseline biological assays. For long-term stock stabilization against asparagine deamidation (Asn2, Asn4), a weakly acidic buffer (such as sterile 0.1% acetic acid) provides maximum solution integrity prior to media dilution.

For Research Use Only. Not for human or animal administration. Not intended to diagnose, treat, cure, or prevent any disease. Sold for laboratory research purposes only.

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