Ask sales for the lot-numbered COA. Net peptide content, RP-HPLC, ESI-MS, or other results appear only when they are part of that batch's agreed analytical scope.
Lot-numbered COA available; the certificate states the tests actually completed.
Batch COA records net peptide content when included in the agreed specification.
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Thymosin β4 (TB-500) fragment preparation · actin-binding region
Overview
TB-500 Fragment is a fragment preparation derived from the TB-500 / Thymosin β4 sequence rather than the full 43-residue peptide. Interest in fragment forms of Thymosin β4 rests on the actin-binding region of the parent molecule, the part of the sequence that carries the actin-sequestering behaviour studied in cell-migration, angiogenesis, and tissue-repair models; a shorter construct is therefore used in research where the question is which portion of the parent sequence drives an observed effect. It is not a synonym for TB-500: the two are separate catalogue items with different fill codes, and a study that intends the full-length 43-mer should order TB-500 rather than this fragment. Because "TB-500 Fragment" is a preparation name rather than a single registered chemical entity, the exact residue span, molecular formula, and mass are established from the batch-specific Certificate of Analysis rather than from the catalogue label. Ask sales for the COA matched to the offered lot and read the sequence span, purity method, counter-ion, and water content actually recorded there. If the buyer's written procedure requires LC-MS/MS sequence coverage to distinguish the fragment from the parent 43-mer or from a near-mass truncation, define that method, acceptance rule, sample, reporting format, timing, and cost before quotation. Fills of 5 mg and 10 mg match the TB-500 vial formats for side-by-side comparison work.
Applications & buyer fit
Repair peptides — BPC-157, TB-500, B7-33, PEG-MGF — ship primarily to research laboratories. The applicable batch COA records the tests actually completed. Tandem-MS sequence evidence is an additional agreed scope when the buyer's written procedure requires it, not a blanket requirement to repeat release testing.
Academic Laboratories
Universities, medical schools, and government research institutes qualifying a reference standard for a method-development or in vivo workflow.
Biotech R&D Groups
Preclinical biotech and pharmaceutical discovery teams sourcing characterized peptides for receptor-pharmacology, screening, and method-development campaigns.
Every release ships with its own batch-specific CoA — identity, purity, and the analytical scope agreed at quote stage, tied to the exact lot you receive.
Review a representative batch CoA before you order, so you can confirm the packet matches what your method or sponsor audit needs.
Supplied strictly as a research reagent to research institutions — not a finished dosage form and not for human administration. Buyer qualification runs at the inquiry stage.
Specifications
Documentation available on request
Regulatory note
A fragment preparation of the TB-500 / Thymosin β4 sequence, carried under a preparation name rather than a single registered CAS. The residue span and identity are recorded on the batch-specific COA and should be confirmed there rather than inferred from the catalogue name; state explicitly at order placement whether the full-length TB-500 or this fragment is intended. Supplied for Research Use Only.
Frequently asked questions
The two are different materials with different fill codes, so the distinction has to be read from the paperwork rather than the name. The batch COA states the sequence span actually supplied, and the intact mass reported by ESI-MS separates a fragment from the 43-residue parent by a wide margin, making a mix-up detectable on inspection. Where the buyer's procedure needs residue-level proof — for example to rule out a truncation of the parent that happens to sit near the fragment mass — LC-MS/MS coverage reads the b- and y-ion ladder across the supplied chain; agree that method, acceptance rule, reporting, timing, and cost with sales before quotation rather than assuming it appears on every lot.
Anchor the comparison to documentation rather than to the shared catalogue name. Confirm on the matching COA which residue span was supplied, the purity method and figure, the counter-ion form, and the Karl Fischer water content, since counter-ion and bound water shift the true peptide mass per vial and therefore the molarity of any reconstituted stock. Record the lot number for both the fragment and the parent in the method file so a later result can be traced to two specific characterized batches, and re-verify identity on each new lot instead of treating lots as interchangeable — for a preparation-name SKU the certificate, not the label, is the identity anchor.
Related peptides
43-mer
Thymosin β4 fragment
15-mer
Body Protection Compound 15-mer
Co-characterized tissue-repair pairing (BPC-157 + TB-500)