Skip to content
Kit presale · 10% offPay before Dec 2
anhydrolabs
0
Compound profiles

KLOW Peptide Blend: What Is in It

The KLOW peptide blend is four peptides in one 80mg vial: GHK-Cu, KPV, BPC-157 and TB-500. What each is, the molar ratios, COA checks and KLOW vs GLOW.

Published · 11 min read · Anhydrolabs

KLOW is not a single peptide. It is a pre-combined blend of four research peptides in one lyophilized vial: GHK-Cu (50 mg), KPV (10 mg), BPC-157 (10 mg) and TB-500 (10 mg), for 80 mg in total. The name is a supplier designation rather than a compound name found in the scientific literature, and no published study has examined the four peptides together.

GLOW, a related blend, contains the same components minus KPV: BPC-157 (10 mg), GHK-Cu (50 mg) and TB-500 (10 mg), 70 mg in total. This article describes each component from primary sources, works out what the labeled masses mean in molar terms, and sets out why a laboratory might, or might not, want a pre-combined vial rather than four separate ones.

What is in a KLOW vial

The compositions below are the ones Anhydrolabs supplies. Masses are as labeled per vial.

ComponentKLOW (80 mg)GLOW (70 mg)Share of KLOW by mass
GHK-Cu50 mg50 mg62.5%
KPV10 mg—12.5%
BPC-15710 mg10 mg12.5%
TB-50010 mg10 mg12.5%
Total80 mg70 mg100%

By this composition, KLOW is the GLOW combination with KPV added. The two blends are otherwise identical, which makes them a natural pair for experiments that need to isolate what the fourth component changes.

What 80mg means on the label

The blend is written several ways: KLOW 80mg, KLOW blend, or the component list GHK-Cu 50mg, KPV 10mg, BPC-157 10mg and TB-500 10mg. All describe the same formulation. The 80mg figure is the sum of the four labeled peptide masses. It is not the mass of any one peptide, and it is not the weight of the lyophilized powder in the vial, which also carries counter-ions and residual water.

KLOW vs GLOW

The GLOW blend is the three-component version: the same 50mg of GHK-Cu and 10mg each of BPC-157 and TB-500, without KPV. Adding 10mg of KPV takes the total from 70mg to 80mg and, because KPV is small, shifts the molar shares more than the mass shares suggest, as the table further down shows.

The four components

GHK-Cu

GHK is the tripeptide glycyl-L-histidyl-L-lysine (Gly-His-Lys), and GHK-Cu is its complex with copper(II). In a 1980 Nature paper, Pickart and colleagues described GHK as a plasma tripeptide that co-isolated with roughly equimolar copper, showed that it readily forms complexes with copper(II), and reported that it enhanced copper uptake into cultured hepatoma cells. They proposed that it acts as a copper transport factor, noting a resemblance to the copper-binding sites of albumin, where copper is held by a histidine next to a basic residue. A 2018 review by Pickart and Margolina summarizes later gene-expression work on GHK in cultured cells.

GHK-Cu is the largest component of both blends by mass. It has its own full profile: GHK-Cu, the copper peptide. Anhydrolabs also supplies it on its own as GHK-Cu.

KPV

KPV is the tripeptide Lys-Pro-Val. PubChem lists it as alpha-MSH (11–13), meaning it is the C-terminal three residues of alpha-melanocyte-stimulating hormone. In a 2008 study in Gastroenterology, Dalmasso and colleagues reported that KPV is taken up into intestinal epithelial cells and T cells by PepT1, a transporter for di- and tripeptides, and that nanomolar concentrations inhibited NF-κB and MAP kinase signaling activation in Caco2-BBE and HT29-Cl.19A intestinal cells and Jurkat T cells stimulated with pro-inflammatory cytokines. The same paper studied KPV in DSS- and TNBS-induced colitis models in mice. It is available on its own as KPV.

BPC-157

BPC-157 is a 15-residue synthetic peptide, Gly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val, described in 1993 as a fragment of a gastric juice protein. No receptor has been identified; cell studies have reported changes in VEGFR2, focal adhesion kinase and growth hormone receptor signaling. The full profile is what is BPC-157.

TB-500

TB-500 is the acetylated heptapeptide Ac-Leu-Lys-Lys-Thr-Glu-Thr-Gln, residues 17 to 23 of thymosin beta-4, taken from the part of that protein that binds actin monomers. Anti-doping chemists first characterized it in the literature in 2012 after identifying it in a commercial product. The full profile is what is TB-500, and it is compared with BPC-157 in BPC-157 vs TB-500.

One caution applies to any research peptide blend that lists TB-500. The name is also used loosely for full-length thymosin beta-4, a 43-residue chain of about 4963 g/mol in PubChem, and some KLOW listings print that longer sequence. The two are different molecules. A certificate of analysis, where one is available, should say which one is in the vial, and the measured mass, about 889 Da for the heptapeptide, settles it.

Identity of each component

Values are from PubChem. For GHK-Cu, PubChem holds several records for different copper complexes; the table uses the 1:1 complex, prezatide copper, and lists free GHK alongside it.

ComponentSequenceFormulaMolecular weightCASPubChem CID
GHK (free peptide)Gly-His-LysC14H24N6O4340.38 g/mol49557-75-773587
GHK-Cu (1:1 complex, prezatide copper)Gly-His-Lys · Cu(II)C14H23CuN6O4+402.92 g/mol89030-95-571587328
KPVLys-Pro-ValC16H30N4O4342.43 g/mol67727-97-3125672
BPC-157GEPPPGKPADDAGLVC62H98N16O221419.5 g/mol137525-51-09941957
TB-500Ac-LKKTETQC38H68N10O14889.0 g/mol885340-08-962707662

What the masses mean in moles

Blend labels are written in milligrams, but cells respond to molar concentrations, and these four molecules differ in size by a factor of about four. Dividing each labeled mass by its molecular weight gives the amount of each peptide in one vial:

ComponentMassApproximate amountShare of KLOW by molesShare of GLOW by moles
GHK-Cu50 mg124.1 µmol72.3%87.2%
KPV10 mg29.2 µmol17.0%—
TB-50010 mg11.25 µmol6.6%7.9%
BPC-15710 mg7.04 µmol4.1%4.9%

Two things stand out. GHK-Cu dominates both blends: roughly 18 molecules of it for every molecule of BPC-157. And the three components labeled at 10 mg are far from equimolar, because KPV is about a quarter the size of BPC-157. Anyone designing an experiment around a blend needs this table, not the milligram figures.

These are nominal figures. They assume the labeled mass is peptide (or, for GHK-Cu, the 1:1 copper complex) rather than a salt with counter-ions and residual water, which is why a measured net content for the lot, where one is available, is a better basis for calculation than the label.

Why a lab might choose a pre-combined blend

A blend is a convenience with trade-offs. The reasons a laboratory might use one:

  • A fixed, reproducible ratio. If an experiment always uses these four components at this ratio, one vial removes four separate weighings and the error that each one adds.
  • One lot, one certificate. All components in a vial share a lot number and are characterized together, which simplifies record-keeping across a series of experiments. For longer series, Anhydrolabs also supplies both blends as 10-vial kits from a single lot.
  • Paired comparisons. Because KLOW and GLOW differ by exactly one component, running them side by side is a direct way to ask what KPV adds to the other three under identical conditions.

And the reasons it may not suit:

  • The ratio cannot be changed. A concentration series for one component moves all four together.
  • Single-component controls need separate vials. A design that asks what each peptide contributes needs the individual compounds, such as BPC-157, TB-500, GHK-Cu and KPV, alongside the blend.
  • Interactions are unstudied. No published work characterizes these four peptides in one solution. Copper(II) is held by GHK, but whether any of it exchanges onto the other peptides in a mixed solution has not been reported, so the blend should be treated as its own test article, not as the sum of four known ones.

Testing a four-component blend

Analytically, a blend is harder than a single peptide, and the certificate should reflect that.

  • Per-component identity. Mass spectrometry should confirm each of the four components separately. Their masses are well spread, from GHK at about 340 Da to BPC-157 at about 1419 Da, so they are straightforward to tell apart.
  • Per-component purity and content. A single purity figure for the whole vial says little. Reversed-phase HPLC can report each component's purity as the area of the principal peak for that component relative to its related impurities, and a quantitative method is needed to confirm that each is present at its labeled amount.
  • Copper. For GHK-Cu, the copper content is part of identity. A certificate may report it, or the copper complex may be confirmed by mass spectrometry.

In practice, a COA for a blend should let the reader verify four things: the identity of each of the individual peptides by mass spectrometry; the purity of each by HPLC, with the chromatography method stated; the net content of each against the label (50mg, 10mg, 10mg and 10mg); and a lot number that matches the vial. Some COAs come from a third-party laboratory and some from the manufacturer. Either way, the document should name the laboratory, the method and the lot, so that a second laboratory could repeat the measurement.

What a complete certificate should contain, and how to read one, is covered in how to read a peptide certificate of analysis.

Handling

Anhydrolabs supplies KLOW and GLOW as lyophilized powders in vacuum-sealed vials. The general rules for dry peptides apply: keep sealed vials frozen, dry and protected from light, and let a cold vial reach room temperature before opening. All four components are water-soluble short peptides or peptide complexes, and aqueous buffers are the usual solvent for in-vitro stocks. Because the blend is dominated by GHK-Cu, buffer components that chelate copper strongly, such as EDTA, could strip copper from the complex, and are worth avoiding unless that is the intent. Divide stocks into single-use aliquots. Temperatures and details are in the storage and handling guide.

Reconstitution follows the usual steps for a lyophilized peptide: run sterile water or buffer down the vial wall, let the cake wet through and swirl gently. Expect color. When you reconstitute a KLOW vial the solution is blue, because copper(II) held by GHK absorbs visible light, as the GHK-Cu profile explains. The other three components are colorless.

Regulatory status

None of the four components is an approved drug in the United States, and neither blend is an approved product. On FDA's Category 2 page for compounding, updated April 22, 2026, BPC-157, TB-500, KPV and GHK-Cu (in an entry limited to certain routes) all appear among nominations withdrawn by the nominators. FDA presented BPC-157, KPV and TB-500 to its compounding advisory committee (PCAC) on July 23, 2026, and proposed that none of them, in free base or acetate form, be included on the 503A bulks list.

In sport, the World Anti-Doping Agency's 2026 Prohibited List names BPC-157 under S0 and TB-500 under S2.3. GHK-Cu and KPV are not named, but S0 covers any pharmacological substance without current regulatory approval for human use, so the absence of a name is not a clearance.

Anhydrolabs supplies both blends for in-vitro laboratory research only, under the terms on the research-use page. Each KLOW blend vial is intended for laboratory research use, for research purposes only, and is not for human or veterinary diagnosis, treatment, or consumption.

For laboratory research use only
Every compound discussed here is supplied as a reference material for in-vitro laboratory research. Not for human or veterinary use. Nothing in this article is guidance for use in a person or an animal. See the research-use statement.

Frequently asked questions

What is the KLOW peptide?

KLOW is a blend of four research peptides in one lyophilized vial: GHK-Cu 50 mg, KPV 10 mg, BPC-157 10 mg and TB-500 10 mg, for 80 mg in total. The name is a supplier designation, not a compound name from the scientific literature.

What is the difference between KLOW and GLOW?

GLOW contains BPC-157 10 mg, GHK-Cu 50 mg and TB-500 10 mg, for 70 mg in total. KLOW is the same combination with 10 mg of KPV added. Otherwise the two are identical.

What does 80mg mean on a KLOW vial?

It is the sum of the labeled peptide masses: GHK-Cu 50mg, KPV 10mg, BPC-157 10mg and TB-500 10mg. It is not the amount of any single peptide. Where a certificate of analysis exists for a lot, the net content it reports for each component is the figure to use in calculations; otherwise the labeled masses are nominal.

Why is the KLOW blend blue?

The color comes from GHK-Cu. Copper(II) bound to the tripeptide absorbs visible light, so both the lyophilized powder and the solution are blue. KPV, BPC-157 and TB-500 are colorless.

Why is GHK-Cu the largest component?

At 50 mg it is the largest by mass, and because it is also the smallest molecule in the blend apart from KPV, it makes up about 72% of KLOW by moles. There are roughly 18 molecules of GHK-Cu for every molecule of BPC-157 in a vial.

Has the KLOW combination been studied?

No published study has examined these four peptides together. Each component has its own literature, mostly in cell culture and animal models, and nothing in that literature describes how they behave in combination.

How is a peptide blend tested?

Each component should be identified separately by mass spectrometry, and its purity and content measured separately, usually by HPLC. A single purity figure for the whole vial is not enough. For GHK-Cu, the copper complex is part of the identity check.

Is KLOW FDA approved?

No. None of its four components is an approved drug. FDA proposed in July 2026 that BPC-157, KPV and TB-500 not be added to the 503A bulks list for compounding.

References

  • Compound profiles

    Tesamorelin: A Stabilized GHRH Analog

    Tesamorelin peptide explained: full-length GHRH(1-44) with a trans-3-hexenoyl cap, why that cap blocks DPP-4, its identity data and FDA status.

    · 9 min read

  • Compound profiles

    Epithalon (Epitalon): The Tetrapeptide Explained

    Epitalon (Epithalon) explained: the Ala-Glu-Asp-Gly sequence, its origin in pineal extract research, the telomerase studies, regulatory status and lab handling.

    · 8 min read

  • Compound profiles

    Thymosin Alpha-1: Structure and Research

    Thymosin alpha 1 peptide profile: the 28-residue N-acetylated sequence, its origin in prothymosin alpha, thymalfasin's regulatory status and lab handling.

    · 8 min read