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TB-500 (Frag)

TB-500 (Frag)

Lyophilised · ≥99% (HPLC) ·

Quantity Volume discounts auto-applied
Custom quantity
1
Shipping to EuropeDispatched from our EU facility in Slovakia, so EU destinations clear no third-country customs. Packeta, DPD or DHL Express depending on country — handling 1–2 business days; typical transit is 1 day in Slovakia, about 2 days to CZ/AT/HU/PL/DE, 1–3 days elsewhere in the EU/EEA, and 2–4 days to non-EU Europe plus local customs. Shipping is calculated at checkout and VAT is shown before you pay.

Supplied lyophilised. Reconstitution typically uses bacteriostatic water.

Independently third-party tested · COA on every batch · 48h EU dispatch
[01]

Overview

Format: lyophilised vial, 2 mg. One sealed vial of freeze-dried TB-500 (Frag), the N-acetylated heptapeptide Ac-LKKTETQ (thymosin β4 residues 17–23), prepared in the laboratory as a solution at the concentration the protocol requires. Looking for fixed, pre-weighed units of the same molecule? That is a separate product: TB-500 Capsules.

Thymosin β4 is a 43-residue actin-sequestering protein, but much of its contact with actin runs through a short central stretch, residues 17–23. TB-500 (Frag) is the synthetic, N-terminally acetylated version of that stretch: the heptapeptide Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln (Ac-LKKTETQ). Analytical laboratories identified this molecule as the active ingredient of preparations sold under the name “TB-500” (Esposito et al., 2012; Ho et al., 2012). It is a different molecule from full-length thymosin β4, which Condor Research lists separately as TB-500 (10 mg vial); the same fragment is also available as a pre-weighed solid in TB-500 Capsules.

Why a seven-residue motif. Mutational mapping placed part of thymosin β4’s actin-binding site in the motif that begins at residue 17 (Van Troys et al., 1996). A review of the protein’s short active sequences attributes its cell-migration, angiogenic and wound-repair activity to the LKKTETQ region — distinct from the N-terminal tetrapeptide Ac-SDKP, whose literature concerns fibrosis and inflammation and which is not this product (Sosne et al., 2010).

What the research explores. The literature on the isolated heptapeptide is small, and most of it used the non-acetylated sequence:

  • Endothelial migration and vessel sprouting (in vitro / ex vivo) — the actin-binding motif matched full thymosin β4 in human umbilical vein endothelial cell migration and chick aortic-arch sprouting assays, while peptides lacking it were inactive (Philp, Huff et al., 2003).
  • Dermal wound models (animal) — a synthetic LKKTETQ peptide promoted repair in aged mice to a degree comparable with the parent protein (Philp, Badamchian et al., 2003).
  • Hepatic stellate cells (in vitro) — the 17–23 peptide, but not the 1–15 peptide, blunted PDGF-BB-driven activation markers, proliferation and migration in human cell cultures (Shah et al., 2018).
  • Metabolism and detection (in vitro, rat, horse) — LC-MS methods identify Ac-LKKTETQ and metabolites such as Ac-LK and Ac-LKK in plasma and urine (Ho et al., 2012; Kwok et al., 2013; Rahaman et al., 2024).

What the evidence does not show. Rahaman et al. (2024) note that the biological effects of the acetylated form itself had not been documented; in their fibroblast assay only the metabolite Ac-LKKTE, not the parent heptapeptide, showed significant wound-closure activity. The human clinical studies often cited in discussions of TB-500 used full-length thymosin β4 — an ophthalmic solution (RGN-259) and a topical formulation in venous ulcers — not this fragment (Sosne & Ousler, 2015; Guarnera et al., 2010). There are no human data for Ac-LKKTETQ, and the findings above do not establish safety or efficacy in humans. Full citations are listed under the Scientific References tab.

Which “TB-500” is which. The name is used in the market for more than one molecule; sequence, mass and CAS number, not the trade name, identify what is in the vial.

Condor Research product Molecule Sequence Length MW (g/mol) CAS
TB-500 (Frag); TB-500 Capsules; the TB-500 in BPC-157 + TB-500, GLOW, KLOW and BPC-157 Arginate + TB-500 Capsules Thymosin β4 fragment 17–23, N-acetylated Ac-LKKTETQ 7 aa 889.0 885340-08-9
TB-500 (10 mg vial) Full-length thymosin β4 Ac-SDKPDMAEIEKFDKSKLKKTETQEKNPLPSKETIEQEKQAGES 43 aa 4963.44 77591-33-4
Not listed by Condor Research Thymosin β4 fragment 1–4 (goralatide) Ac-SDKP 4 aa 487.5 120081-14-3

Physicochemical profile. CAS 885340-08-9 · Molecular formula C₃₈H₆₈N₁₀O₁₄ · Molecular weight 889.0 g/mol · Sequence Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln (thymosin β4 residues 17–23, N-terminally acetylated) · Appearance: white lyophilized powder · Soluble in water.

Specification & quality. Each individually sealed vial contains 2 mg of TB-500 (Frag) — Ac-LKKTETQ — as a white lyophilized powder at ≥99% purity by HPLC. Every batch is third-party tested, with a Certificate of Analysis (COA) available. Store at −20 °C, protected from light and moisture.

This product is intended for laboratory research use only (RUO). It is not a drug, food, cosmetic, or dietary supplement, and is not for human or veterinary use, ingestion, or diagnostic application. Handling is restricted to qualified research professionals operating in an appropriately equipped laboratory.

When the TB-500 (Frag) lyophilised vial is the right format

  • One quantity, concentration chosen at the bench. The 2 mg cake (about 2.25 µmol at 889.0 g/mol) is reconstituted with a suitable diluent, so the working concentration follows the assay and not a fixed unit mass.
  • Reference-standard work. Detection work on this heptapeptide (Esposito et al., 2012; Ho et al., 2012) is done by LC-MS on solutions; a vial supplies the single reference quantity from which a stock and its dilution series are prepared.
  • Storage before and after preparation. Keep the sealed vial at −20 °C, protected from light and moisture; in solution, stability depends on the diluent and the temperature, which is why a vial suits stock prepared on demand.

Need identical pre-weighed units for replicate or blinded designs? TB-500 Capsules hold the same molecule (60 × 500 mcg per bottle) and are sold separately. Both formats carry the fragment, not the full-length thymosin β4 of the TB-500 10 mg vial. For laboratory research use only. Not for human or veterinary use.

Supplied for in-vitro laboratory research use only (RUO). Not a drug, food or supplement; not for human or veterinary use.

[04]

Quality & COA

Certificate of Analysis
Lot-specific COA with every order

Certificate of Analysis — lot-specific COA ships with every order and is available on request.

Each lot is tested by an independent third-party laboratory for identity (mass spectrometry) and purity (HPLC). The Certificate of Analysis for your specific batch ships with the order and is available on request — no house data, no exceptions.

HPLC purity
≥99% (HPLC)
Method
HPLC + MS
Endotoxin
Reported
[02]

Data Sheet

CAS number885340-08-9
Molecular formulaC₃₈H₆₈N₁₀O₁₄
Molecular weight889.0
SequenceAc-Leu-Lys-Lys-Thr-Glu-Thr-Gln (Ac-LKKTETQ; thymosin β4 residues 17–23)
Purity≥99% (HPLC)
Physical formWhite lyophilized powder
Quantity2mg/vial
SolubilitySoluble in water
StorageStore at -20°C, protect from light
Shelf life24 months from manufacture date
OriginEU · Slovakia
ClassificationResearch use only
[03]

Scientific References

01 Esposito S, Deventer K, Goeman J, Van der Eycken J, Van Eenoo P. Synthesis and characterization of the N-terminal acetylated 17-23 fragment of thymosin beta 4 identified in TB-500, a product suspected to possess doping potential. Drug Test Anal. 2012;4(9):733-8. PMID: 22962027. doi:10.1002/dta.1402. PubMed 02 Ho EN, Kwok WH, Lau MY, Wong AS, Wan TS, Lam KK, et al. Doping control analysis of TB-500, a synthetic version of an active region of thymosin β₄, in equine urine and plasma by liquid chromatography-mass spectrometry. J Chromatogr A. 2012;1265:57-69. PMID: 23084823. doi:10.1016/j.chroma.2012.09.043. PubMed 03 Kwok WH, Ho EN, Lau MY, Leung GN, Wong AS, Wan TS. Doping control analysis of seven bioactive peptides in horse plasma by liquid chromatography-mass spectrometry. Anal Bioanal Chem. 2013;405(8):2595-606. PMID: 23318763. doi:10.1007/s00216-012-6697-9. PubMed 04 Rahaman KA, Muresan AR, Min H, Son J, Han HS, Kang MJ, et al. Simultaneous quantification of TB-500 and its metabolites in in-vitro experiments and rats by UHPLC-Q-Exactive orbitrap MS/MS and their screening by wound healing activities in-vitro. J Chromatogr B Analyt Technol Biomed Life Sci. 2024;1235:124033. PMID: 38382158. doi:10.1016/j.jchromb.2024.124033. PubMed 05 Philp D, Huff T, Gho YS, Hannappel E, Kleinman HK. The actin binding site on thymosin beta4 promotes angiogenesis. FASEB J. 2003;17(14):2103-5. PMID: 14500546. doi:10.1096/fj.03-0121fje. PubMed 06 Philp D, Badamchian M, Scheremeta B, Nguyen M, Goldstein AL, Kleinman HK. Thymosin beta 4 and a synthetic peptide containing its actin-binding domain promote dermal wound repair in db/db diabetic mice and in aged mice. Wound Repair Regen. 2003;11(1):19-24. PMID: 12581423. doi:10.1046/j.1524-475x.2003.11105.x. PubMed 07 Sosne G, Qiu P, Goldstein AL, Wheater M. Biological activities of thymosin beta4 defined by active sites in short peptide sequences. FASEB J. 2010;24(7):2144-51. PMID: 20179146. doi:10.1096/fj.09-142307. PubMed 08 Van Troys M, Dewitte D, Goethals M, Carlier MF, Vandekerckhove J, Ampe C. The actin binding site of thymosin beta 4 mapped by mutational analysis. EMBO J. 1996;15(2):201-10. PMID: 8617195. PubMed 09 Shah R, Reyes-Gordillo K, Rojkind M. Thymosin β4 inhibits PDGF-BB induced activation, proliferation, and migration of human hepatic stellate cells via its actin-binding domain. Expert Opin Biol Ther. 2018;18(sup1):177-184. PMID: 30063851. doi:10.1080/14712598.2018.1478961. PubMed 10 Lu P, Shan M, Peng C, Ji W, Yang T, Yang Z, et al. Alkaline Phosphatase-Triggered Spatiotemporal Repair of Corneal Injury with TB500 Peptide Hydrogel. ACS Appl Mater Interfaces. 2025;17(50):67503-67518. PMID: 41359360. doi:10.1021/acsami.5c14652. PubMed 11 Sosne G, Ousler GW. Thymosin beta 4 ophthalmic solution for dry eye: a randomized, placebo-controlled, Phase II clinical trial conducted using the controlled adverse environment (CAE™) model. Clin Ophthalmol. 2015;9:877-84. PMID: 26056426. doi:10.2147/OPTH.S80954. PubMed 12 Guarnera G, DeRosa A, Camerini R. The effect of thymosin treatment of venous ulcers. Ann N Y Acad Sci. 2010;1194:207-12. PMID: 20536470. doi:10.1111/j.1749-6632.2010.05490.x. PubMed 13 Mendias CL, Awan TM. Safety and Efficacy of Approved and Unapproved Peptide Therapies for Musculoskeletal Injuries and Athletic Performance. Sports Med. 2026;56(8):1921-1935. PMID: 41966639. doi:10.1007/s40279-026-02437-0. PubMed 14 Mayfield CK, Bolia IK, Feingold CL, Lin EH, Liu JN, Rick Hatch GF, et al. Injectable Peptide Therapy: A Primer for Orthopaedic and Sports Medicine Physicians. Am J Sports Med. 2026;54(1):223-229. PMID: 41476424. doi:10.1177/03635465251357593. PubMed 15 Rahman OF, Lee SJ, Seeds WA. Therapeutic Peptides in Orthopaedics: Applications, Challenges, and Future Directions. J Am Acad Orthop Surg Glob Res Rev. 2026;10(1). PMID: 41490200. doi:10.5435/JAAOSGlobal-D-25-00236. PubMed

References are illustrative of the research literature surrounding this compound. All claims relate to in-vitro and animal models only.

[05]

FAQ

It is the same molecule, Ac-LKKTETQ (thymosin β4 residues 17–23), in a different format. This listing is a 2 mg lyophilised vial that the laboratory reconstitutes to its own working concentration. TB-500 Capsules are a separate product holding 60 pre-weighed units of 500 mcg (30 mg per bottle) for protocols that need identical units. Neither is the full-length thymosin β4 sold as the TB-500 10 mg vial. For laboratory research use only. Not for human or veterinary use.

TB-500 (Frag) is the synthetic heptapeptide Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln (Ac-LKKTETQ; CAS 885340-08-9; 889.0 g/mol), the N-terminally acetylated form of residues 17–23 of thymosin β4 — the region of the protein involved in actin binding. Condor Research supplies it as a 2 mg lyophilized vial at ≥99% HPLC purity, strictly for in-vitro laboratory research use only.

They are different molecules. TB-500 (Frag) is the 7-residue Ac-LKKTETQ fragment (889.0 g/mol, CAS 885340-08-9). Condor Research's TB-500 (10 mg vial) is full-length synthetic thymosin β4: 43 residues, 4963.44 g/mol, CAS 77591-33-4. The fragment reproduces only the central actin-binding motif, not the rest of the protein. Each is a separate ≥99% HPLC, research-use-only reference compound with its own COA.

TB-500 (Frag) is supplied as a 2 mg vial and the full-length TB-500 as a 10 mg vial; the masses are analytical reference quantities for two distinct molecules, not doses. Because the fragment is about 5.6 times lighter than full thymosin β4 (889.0 vs 4963.44 g/mol), the 2 mg vial (≈2.2 µmol) and the 10 mg vial (≈2.0 µmol) hold similar molar amounts. For current pricing, contact info@condorresearch.com. Both are ≥99% HPLC research-use-only materials.

No. Ac-SDKP (N-acetyl-Ser-Asp-Lys-Pro, also called goralatide, CAS 120081-14-3) is the N-terminal tetrapeptide of thymosin β4 and a separate molecule with its own antifibrotic literature. TB-500 (Frag) is Ac-LKKTETQ, residues 17–23 of the same parent protein. The two fragments come from different regions and are studied for different questions (Sosne et al., 2010). Condor Research does not list Ac-SDKP. Research use only.

TB-500 (Frag) is the 7-residue Ac-LKKTETQ fragment of thymosin β4, studied around the actin-binding motif involved in cell migration, while BPC-157 is a 15-residue gastric pentadecapeptide studied for cytoprotective mechanisms. They are both short peptides in regenerative research but have unrelated sequences and pathways. Condor Research offers each as a distinct ≥99% HPLC, research-use-only reference compound; the choice depends on your experimental target.

TB-500 (Frag) is selected when the research question is specifically the 17–23 actin-binding motif — for example comparing it with the intact protein in migration assays, or using it as an analytical reference standard for LC-MS detection of Ac-LKKTETQ and its metabolites. Full-length TB-500 is the reference when the whole 43-residue protein is the object of study. Both remain research-use-only reference materials with no human or veterinary application.

Yes. The acetylated heptapeptide Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln (CAS 885340-08-9; 889.0 g/mol, expected [M+H]+ ≈ 889.5 m/z) is verified for each lot by an independent third-party laboratory using HPLC for purity and mass spectrometry for identity, confirming both the sequence and N-terminal acetylation. Results are documented on the batch-specific Certificate of Analysis, available on request at info@condorresearch.com.

Yes. TB-500 (Frag) is supplied strictly for laboratory research use only (in vitro). It is not a medicine, food, supplement, cosmetic, or medical device, and is not for human or veterinary use, administration, or consumption. Condor Research provides no dosing, protocols, or human-use guidance. Purchase is limited to qualified professionals and institutions aged 18 or over.

Yes. Each TB-500 (Frag) lot is tested by an independent third-party laboratory by HPLC for identity and purity, with mass spectrometry confirmation, and ships against a batch-specific Certificate of Analysis verifying ≥99% purity. To request the COA for the current lot before ordering, contact info@condorresearch.com.

For analytical laboratory preparation only, TB-500 (Frag) is water-soluble and can be reconstituted with a sterile aqueous diluent; with a 2 mg vial the chosen volume sets the working concentration. Store the sealed lyophilized vial at -20°C, protected from light, with a 24-month shelf life. This is laboratory handling information, not guidance for any human or animal use.

Condor Research supplies TB-500 (Frag) directly, dispatched from our EU facility in Slovakia to the EU, EEA, UK and Switzerland. Deliveries to EU destinations clear no third-country customs, and shipping is calculated at checkout. Supplied strictly as a research-use-only reference material — not for human or veterinary use.

[06]

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