What is the BPC-157 / TB-500 Blend?
This is a two component mixture supplied as lyophilised powder for laboratory research. BPC-157 and TB-500 are synthesised separately and then co-lyophilised into a single vial at a fixed stated ratio.
Components
BPC-157 is a synthetic pentadecapeptide, a fifteen residue sequence corresponding to a partial fragment of a protein described in gastric juice. TB-500 corresponds to the acetylated actin binding region of thymosin beta-4.
The designation TB-500 is applied inconsistently across the supply chain. Some suppliers use it for the acetylated fragment and others for the full length protein. The certificate of analysis for the lot confirms which species is present by LC-MS, and it is worth reading before assuming which molecule is in the vial.
Why a co-lyophilised mixture
A mixture prepared from one cake enters solution in a single step rather than being combined from two separately weighed and diluted stocks. For comparative work that includes a mixture condition alongside single compound conditions, this removes one source of preparation variance between the arms.
The ratio is fixed at the point of manufacture and cannot be varied after supply. Where a design requires the two concentrations to vary independently, the single compound listings for BPC-157 and TB-500 are the correct format instead.
Specification figures for the blend
The component quantities, sequences, molecular formulae and molecular weights for the lot supplied are stated on its certificate of analysis. Published figures for research compounds are not always consistent between sources, so this page defers to the certificate rather than restating a value that may not match the material in the vial.
Working with a multi component reference
Purity and identity are established per component rather than for the mixture as a whole, so a single figure does not describe this material. Read each component line on the certificate separately. Net peptide content per component is also stated there, and it is the figure to work from when calculating concentrations rather than the labelled quantity.
Analysis and certification
Each lot of the blend is analysed by an independent laboratory using RP-HPLC with LC-MS identity confirmation before it is released for sale. Both analyses are carried out per component. The certificate of analysis is published against the lot number rather than the product page, so the document you read is the document for the vial you receive.
Research use only
NH Peptides supplies this blend as an analytical reference material for laboratory research. It is not supplied for any use in humans or animals, and no information on this page describes or implies any such use.
| Product |
BPC-157 / TB-500 Blend |
| Class |
Co-lyophilised two component peptide mixture |
| Components |
BPC-157 and TB-500 |
| Component quantities |
Stated on the certificate of analysis |
| Sequences |
Stated on the certificate of analysis |
| CAS numbers |
Stated on the certificate of analysis |
| Molecular formulae |
Stated on the certificate of analysis |
| Molecular weights |
Stated on the certificate of analysis |
| Appearance |
White to off white lyophilised powder |
| Purity specification |
≥99% per component |
| Identity method |
LC-MS, per component |
| Purity method |
RP-HPLC, per component |
| Labelled quantity |
20mg total, stated on the vial label |
How the blend is tested
Two separate analyses are carried out on every lot before it is released, and both appear on the certificate. Identity is confirmed by LC-MS against the expected mass for each sequence. Purity is determined by RP-HPLC peak area.
Both analyses are reported per component. A multi component reference does not have a single purity figure, so the certificate carries one line per component rather than one figure for the vial.
Purity specification for the blend
Lots are released against a ≥99% purity specification applied to each component individually, determined by RP-HPLC peak area. The figures for the lot you receive are stated on its certificate of analysis and may differ from the specification.
A specification is a release threshold, not a description of every lot. Where a measured figure and the specification differ, the certificate is the record that applies to your material. Analytical figures relate to the lot they are published against and carry no implication of suitability for any purpose beyond laboratory research.
Storing the blend
Lyophilised material is shipped under cold chain and should be returned to freezer storage on arrival. Store the sealed vial dry at −20°C or below, protected from light and moisture.
Allow the vial to reach room temperature before breaking the seal, so that moisture does not condense onto the cake.
Preparing stock solutions
Prepare stock solutions in sterile water or an appropriate aqueous buffer for analytical work, at a concentration suited to your assay. Confirm solubility against the certificate of analysis before preparing stocks.
Introduce solvent slowly against the vial wall rather than directly onto the cake, and allow the material to dissolve without agitation. Do not vortex.
Because the vial holds two components, concentrations should be calculated from the per component net peptide content on the certificate rather than from the total labelled quantity. Both components enter solution together and cannot be separated after reconstitution.
Peptide solutions are less stable than lyophilised powder. Prepare close to the point of use, hold at 2–8°C for short periods only, and avoid repeated freeze and thaw cycles. Adsorption to plastic surfaces can reduce effective concentration in dilute working solutions, so use low binding consumables where the assay is sensitive to this.
Handling and disposal
Assess the hazards of this material before handling and use appropriate controls and protective equipment. It has not been characterised toxicologically and should be treated as potentially hazardous.
Record the lot number from the vial label in your own inventory alongside the certificate of analysis, storage temperature and disposal route, so that your records remain auditable after the order closes.
Dispose of unused material, vials and packaging lawfully and in line with your institution’s waste procedures. Do not dispose to drain.