Specification
Certificate of analysis
Every box carries a batch number. Look it up and you get the analytical data for the exact vials you received.
Batch lookup →TB-500
Thymosin β-4 fragment (Ac-SDKP related)
The synthetic analogue of thymosin beta-4, the principal actin-sequestering peptide in eukaryotic cells and a long-studied regulator of tissue repair.
What the literature describes
Thymosin beta-4 (Tβ4) is the major G-actin-sequestering molecule in mammalian cells. Its actin-binding domain has been mapped to the sequence that TB-500 reproduces. Published work reports that Tβ4 accelerates re-epithelialisation, upregulates matrix metalloproteinase expression during remodelling, acts as a chemoattractant for myoblasts after muscle injury, and promotes angiogenesis through its actin-binding site. In rodent incisional wound models, locally applied Tβ4 healed with minimal scarring and no loss of wound breaking strength.
Available sizes & pricing
Prices in USD per sealed box of 10 vials. Bulk pricing available from 10 boxes — see wholesale.
| Vial strength | Box | Price | |
|---|---|---|---|
| 2mg | 10 vials |
$43
$4.30 per vial
|
Order 2mg |
| 5mg | 10 vials |
$83
$8.30 per vial
|
Order 5mg |
| 10mg | 10 vials |
$163
$16.30 per vial
|
Order 10mg |
Published research
Links open peer-reviewed sources on PubMed. These are provided so you can read the primary literature yourself. Citing a study is not a claim that this compound is safe or effective for any use in humans.
- Thymosin beta-4: actin-sequestering protein moonlights to repair injured tissuesPubMed
- Thymosin beta-4 accelerates wound healingPubMed
- Thymosin u03b24: a multi-functional regenerative peptide u2014 basic properties and clinical applicationsPubMed
- The actin binding site on thymosin beta-4 promotes angiogenesisPubMed
- Muscle injury-induced thymosin u03b24 acts as a chemoattractant for myoblastsPubMed
- All indexed literature on thymosin beta 4 (PubMed search)PubMed search
Research areas
Studied in the same area
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The classic paired blend: a GHRH analog alongside a selective ghrelin-receptor agonist, studied for complementary action on the GH axis.