Skip to main content

Qualified laboratory research use only. Not for human or veterinary use, consumption, administration, compounding, diagnosis, or treatment.

RESEARCH USE ONLY
TB-500 Vespera catalog photography

Research material profile

TB-500

Thymosin-β4 fragment research peptide

TB-500 is used in current FDA materials for the N-acetylated seven-amino-acid sequence LKKTETQ, a fragment corresponding to residues 17–23 of full-length thymosin β4.

Identity shorthand
Ac-LKKTETQ
Evidence map
Identity-sensitive preclinical evidence
Public page scope
Identity and literature context; no purchase offer
Commerce accessQualified laboratory buyers only

Pricing, availability, ordering, cart, and checkout remain inside the reviewed qualified-access portal.

Qualified catalog access

Plain-language identity

What TB-500 is

TB-500 is used in current FDA materials for the N-acetylated seven-amino-acid sequence LKKTETQ, a fragment corresponding to residues 17–23 of full-length thymosin β4.

Research class
Thymosin-β4 fragment research peptide
Sequence / identity shorthand
Ac-LKKTETQ
Evidence map
Identity-sensitive preclinical evidence
Identity boundary

“TB-500,” “TB4,” full-length thymosin β4, and the LKKTETQ fragment are not interchangeable names. A lot record must identify which molecular species was actually analyzed.

What researchers examine

  • Actin-binding-domain behavior and cell migration in controlled model systems.
  • Endothelial sprouting, matrix remodeling, and repair-associated assays.
  • Differences between full-length thymosin β4 literature and fragment-specific experiments.

How to read the evidence

  • A 2003 study linked the central actin-binding motif of thymosin β4 to endothelial migration and sprouting assays.
  • A separate 2003 animal study evaluated full-length thymosin β4 and the LKKTETQ fragment in wound-repair models.
  • Results obtained with full-length thymosin β4 cannot automatically be assigned to a shorter fragment or to a catalog item with an unverified sequence.

What this evidence does not establish

  • Published repair-related findings are largely cellular or animal-model observations and are not personal-use guidance.
  • Identity ambiguity is a central interpretation risk; the lot-specific sequence and form must be confirmed.
  • This Vespera record makes no claim of clinical safety, efficacy, sterility, or suitability for administration.

Documentation checklist

  • Confirm whether the specification identifies the seven-residue fragment, full-length thymosin β4, or another related material.
  • Match sequence/form, SKU, strength, lot, method, and reported mass or purity information.
  • Keep literature on full-length and fragment materials separated in the research record.

Primary and official sources

Links are provided for source review. A citation is not an endorsement of nonresearch use.

  1. FDA briefing document — TB-500-related bulk drug substances (2026)Identity discussion distinguishing TB-500 from full-length thymosin β4.
  2. Malinda et al. — thymosin β4 actin-binding site and angiogenesis assays (2003)Cell migration and vessel-sprouting model systems.
  3. Philp et al. — thymosin β4 and LKKTETQ in animal wound models (2003)Animal-model study; not evidence of human use.
Research use only. This profile contains identity and literature context only. It provides no dosing, administration, reconstitution, diagnosis, treatment, or personal-use guidance.