TB-500 (Thymosin β4 fragment)

TB-500 Studied Effects in the Literature

Reviewed by our laboratory team · Last updated 2026-07-03

Peer-reviewed literature reports TB-500 (and full-length Tβ4) effects on actin sequestration, cell migration, angiogenesis, and tissue-repair endpoints in animal wound and infarct models. Findings are in vitro and in vivo animal data; clinical human evidence remains limited.

Key facts

Cell migration
In vitro and animal
Angiogenesis
Corneal and vascular models
Wound repair
Dermal and cardiac animal models

How to read the literature

Distinguish TB-500 fragment studies from full-length Tβ4 studies. Many landmark findings used recombinant Tβ4; extrapolation to the shorter fragment is imperfect.

Extended research context

The TB-500 (Thymosin β4 fragment) deep dive

Deep dive: TB-500 vs full-length Thymosin Beta-4

'TB-500' is a synthetic peptide corresponding to the active 17-amino-acid actin-binding region of the endogenous 43-residue Thymosin Beta-4 protein. The two are not identical — TB-500 lacks the flanking sequence that gives full-length TB-4 additional binding partners. In the research literature, papers use 'Thymosin β4' when they mean the full protein and 'TB-500' or 'AcSDKP fragment' when they mean the shorter synthetic peptide. Reading a CoA carefully to see which molecule is in the vial matters — mass spec is the definitive check.

Actin-binding as the core mechanism

The N-terminal region of TB-4 (and TB-500 by inheritance) contains the canonical actin-binding motif. This motif sequesters G-actin monomers, modulating the G:F actin equilibrium in cell cultures. That mechanism is why almost every mechanistic paper on TB-500 traces back to cytoskeletal reorganisation, cell migration, and models of tissue repair.

Handling considerations unique to TB-500

TB-500 is a 17-residue peptide with modest amphipathicity; it reconstitutes cleanly in bacteriostatic water but is sensitive to repeated freeze/thaw. Aliquoting into single-use volumes on first reconstitution preserves potency across a batch. HPLC on the batch CoA should show a single dominant peak; a doublet suggests deamidation.

Research applications

  • In vitro actin-polymerisation assays (G:F actin ratio measurement)
  • Cell-migration and wound-scratch assays in fibroblast lines
  • Angiogenesis models: tube-formation and endothelial migration assays
  • Analytical method development for short peptides on RP-HPLC
  • Reference-material comparisons against endogenous Thymosin β4

Handling checklist

  • Store lyophilised vials at −20 °C long-term
  • Reconstitute with bacteriostatic water (0.9% benzyl alcohol)
  • Aliquot immediately to avoid freeze/thaw cycles
  • Refrigerate reconstituted aliquots at 2–8 °C; use within 28 days
  • Confirm mass (~4,963 Da for TB-500) via CoA before study use

Common research-handling mistakes

Learnt from thousands of researcher orders across our UK labs.

Assuming TB-500 = full Thymosin β4

Fix: TB-500 is the 17-residue actin-binding fragment; check the CoA sequence.

Repeated freeze/thaw

Fix: Aliquot at first reconstitution; each cycle degrades yield.

Using tap water

Fix: Use bacteriostatic or sterile water only.

Continue researching

Peer-reviewed guides, comparators and matched reference materials.

Related questions researchers ask

  • Is TB-500 the same as Thymosin Beta-4?
  • How does TB-500 bind actin?
  • What is the molecular weight of TB-500?
  • How is TB-500 reconstituted for research?
  • Is TB-500 legal to buy in the UK for research?

Frequently asked questions

Are there human trials?
Limited early-phase trials with full-length Tβ4 exist; TB-500 fragment specifically has minimal clinical data.

Primary sources & clinical trials

Peer-reviewed research and registered trials from PubMed, ClinicalTrials.gov, PubChem, FDA and NIH. All links open in a new tab (external, rel="nofollow").

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Research use only. The information above is provided for scientific and educational reference. Compounds referenced are not approved for human use and are supplied for in vitro research or reference-material purposes only. No efficacy, safety, or therapeutic claims are made.