Cartalax 20 mg (AED; Ala–Glu–Asp) from Peptide Tech is a premium, lyophilized research-use-only (RUO) tripeptide supplied at ≥99% purity (HPLC & MS verified). The sequence H-Ala-Glu-Asp-OH is prepared for rigorous in-vitro studies in fibroblast/chondrocyte biology, extracellular-matrix readouts, and analytical method development—backed by lot traceability, independent third-party testing, and validated cold-chain logistics.
Specifications
| Property | Details |
|---|---|
| Product | Cartalax — lyophilized peptide, 20 mg |
| Chemical Name | H-Ala-Glu-Asp-OH (L-alanyl-L-glutamyl-L-aspartic acid) |
| Synonyms | AED; T-31; Ala-Glu-Asp |
| Sequence | Ala–Glu–Asp (A-E-D) |
| CAS Number | Not assigned (sequence-defined RUO tripeptide) |
| PubChem CID | 87815447 |
| Molecular Formula | C12H19N3O8 |
| Molecular Weight | ≈ 333.29 g/mol |
| Appearance | White to off-white lyophilized powder |
| Container | 3 mL Type I glass vial; butyl stopper; flip-off seal |
| Purity / Identity | ≥99% by HPLC; identity by MS (batch COA via on-vial QR) |
| Counter-ion | Typically acetate (verify on lot COA) |
| Solubility | Soluble in sterile water or neutral buffers; for rapid wetting at higher concentrations, pre-wet with ≤0.1% acetic acid, then bring to buffer. If sterility is required by your SOP, filter (0.22 µm). |
| Storage (lyophilized) | −20 °C long-term; store desiccated and protected from light. |
| After Reconstitution | Aliquot; store at ≤ −20 °C (or −80 °C per SOP); avoid repeat freeze–thaw cycles. |
| Intended Use | RUO only. Not for human or animal use. |
Molecular Structure
View on PubChem (CID 87815447)
Key Features of Peptide Tech
- Same-Day Shipping (Mon–Fri, on in-stock items)
- GMP-Aligned lyophilization & documentation
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- Batch QR for instant COA & chain-of-custody verification
- 3rd-Party U.S. Lab Testing — purity, quantity, endotoxin
- Cold-Chain Shipping — Always (no paid upgrade)
- Worldwide Shipping; all major payments accepted
- Text & Email order updates; 2-Day FedEx/UPS standard with low-cost overnight
- Largest Variety of peptides & bioregulators
Potential Applications in Research (RUO)
Strictly for laboratory research. No health, diagnostic, or therapeutic claims.
- Fibroblast assays (proliferation & senescence panels): quantify Ki-67, CDKN1A (p21), and p53 signaling with AED exposure in human dermal or lung fibroblasts; include apoptosis markers (Annexin V/PI) and NF-κB reporter readouts for pathway mapping.
- Chondrocyte matrix & phenotype readouts: evaluate COL2A1, ACAN, and MMP13 by RT-qPCR/ELISA; apply pellet culture with histology (Safranin O/fast green) to track glycosaminoglycan and type-II collagen content.
- Cell-migration (scratch) assays: perform standardized wound-closure assays in fibroblast monolayers to assess migration dynamics under controlled AED dosing and serum conditions.
- Peptide–DNA interaction workflows: model or test short peptide interactions with defined promoter motifs using fluorescence quenching/displacement or EMSA; compare against literature-reported sequence preferences for short peptides.
- Analytical method development: establish RP-HPLC/LC-MS(/MS) identity, purity, recovery, and forced-degradation stability across buffers, pH, and temperature to validate lab SOPs.
Citations (selected)
- Liang, Chun-Chi, Ann Y. Park, and Jun-Lin Guan. “In Vitro Scratch Assay: A Convenient and Inexpensive Method for Analysis of Cell Migration in vitro.” Nature Protocols, vol. 2, no. 2, 2007, pp. 329–333. https://doi.org/10.1038/nprot.2007.30.
- Wu, Ling, Janine N. Post, and Marcel Karperien. “Engineering Cartilage Tissue by Pellet Coculture of Chondrocytes and Mesenchymal Stromal Cells.” Methods in Molecular Biology, vol. 1226, 2014, pp. 31–41. https://doi.org/10.1007/978-1-4939-1619-1_4.
- Caputi, Sergio, et al. “Effect of Short Peptides on Neuronal Differentiation of Stem Cells.” International Journal of Immunopathology and Pharmacology, vol. 33, 2019, pp. 1–12. https://doi.org/10.1177/2058738419828613.
- Fedoreyeva, L. I., et al. “Penetration of Short Fluorescence-Labeled Peptides into the Nucleus in HeLa Cells and in vitro Specific Interaction of the Peptides with Deoxyribooligonucleotides and DNA.” Biochemistry (Moscow), vol. 76, no. 11, 2011, pp. 1210–1219. https://doi.org/10.1134/S0006297911110022.
- Khavinson, V. Kh., N. S. Lin’kova, and S. I. Tarnovskaya. “Short Peptides Regulate Gene Expression.” Bulletin of Experimental Biology and Medicine, vol. 162, 2016, pp. 288–292. https://doi.org/10.1007/s10517-016-3596-7.
Quality, Storage & Handling
Every lot is confirmed by HPLC (purity) and MS (identity); the on-vial QR links to the batch COA. Independent U.S. labs verify purity, quantity, and endotoxin.
- Storage (lyophilized): −20 °C long-term or 2–8 °C short-term; keep desiccated and protected from light.
- After reconstitution: Aliquot and store at ≤ −20 °C (or −80 °C per SOP); avoid repeated freeze–thaw cycles.
- Reconstitution tips: Use sterile water or compatible buffer; gently swirl/invert to dissolve. If your SOP requires sterility, 0.22 µm filter and aliquot promptly.
Shipping & Fulfillment
Ships with validated cold-chain packaging. In-stock orders placed before the daily cutoff ship the same day. 2-Day FedEx/UPS is standard, with overnight options available. Automated text/email updates included; international shipping available where permitted.
Compliance & RUO Disclaimer
For laboratory research only. Not a drug, cosmetic, food, or household chemical. Not for human or animal use, ingestion, diagnostic, or therapeutic applications. Purchasers warrant appropriate qualifications and compliance with applicable regulations and institutional policies.
FAQs
- Is Cartalax the same as Chonluten, Vesugen, or Vilon?
- No. Cartalax is the tripeptide Ala–Glu–Asp (AED). Chonluten is Glu–Asp–Pro (EDP), Vesugen is Lys–Glu–Asp (KED), and Vilon is Lys–Glu (KE). Confirm the sequence required by your assay.
- Do you provide a PubChem image?
- Yes—the 2D structure above is rendered from PubChem CID 87815447 for AED (Ala–Glu–Asp).
- What purity do you provide?
- Each 20 mg vial is ≥99% by HPLC with MS identity confirmation; third-party testing is performed on every lot (COA via on-vial QR).
- How should I reconstitute it?
- Dissolve in sterile water or a compatible buffer; gently invert until fully dissolved. If your SOP requires sterility, 0.22 µm filter and aliquot to avoid repeat freeze–thaw.
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