UPB Glow Blend ( BPC-157 10mg + TB500 10mg + GHK Cu 50mg)

UPB Glow Blend — BPC-157, TB-500 & GHK-Cu

UPB Glow Blend is a three-component research product supplied as a blue lyophilized powder. Each vial is labeled with BPC-157 10 mg, TB-500 10 mg, and GHK-Cu 50 mg, providing 70 mg of total labeled content.

The linked Certificate of Analysis documents component identity, purity, net content, endotoxin testing, and microbial screening for the submitted samples. Match the lot number on the vial to the report before using these results in laboratory records.

Purity

The Certificate of Analysis reports 99.71% purity by HPLC-UV. Identity testing by liquid chromatography–mass spectrometry (LC-MS) confirms GHK-Cu, TB-500, and BPC-157.

The report provides one purity result for the analyzed blend. It does not provide separate purity percentages for each component.

Form

Blue lyophilized powder. This appearance is documented in the laboratory report.

Quantity

Total labeled content: 70 mg per vial.

• BPC-157: 10 mg labeled quantity
• TB-500: 10 mg labeled quantity
• GHK-Cu: 50 mg labeled quantity

The COA provides the following measured net content for two submitted vials:

• Vial 1: BPC-157 10.65 mg, TB-500 11.01 mg, and GHK-Cu 57.22 mg
• Vial 2: BPC-157 10.44 mg, TB-500 10.52 mg, and GHK-Cu 55.32 mg

The report’s analytical summary lists BPC-157 10.54 mg, TB-500 10.77 mg, and GHK-Cu 56.27 mg. These measurements describe the submitted samples and do not guarantee identical content in every vial.

Batch / Lot Number

11020-005

The linked analytical results apply to this lot. Use documentation matching the lot number printed on your supplied product.

Certificate of Analysis

• Testing laboratory: Freedom Diagnostics
• Client: Ultra Pure Bioscience
• Product submitted: Glow 50/10/10mg
• Accession number: 2607170627
• Search code: Ultr2607170627
• Received date: July 17, 2026
• Reported date: July 21, 2026
• Lot number: 11020-005
• Identity: GHK-Cu, TB-500, and BPC-157 confirmed by LC-MS
• Purity: 99.71% by HPLC-UV
• Endotoxin testing: Pass for both reported replicates
• Microbial analysis: No detectable microbial DNA by the reported PCR assay

Read the original Glow Blend Certificate of Analysis.

Endotoxin testing used a Limulus Amebocyte Lysate assay, with an assay sensitivity listed as ≤0.05 EU/mL. Microbial screening used a PCR-based assay targeting common microbial contaminants. These findings are limited to the tests performed and do not establish sterility.

Handling & Storage

Follow the manufacturer’s product-specific handling instructions and your laboratory’s established procedures.

The supplied COA does not specify storage temperatures, shelf life, or conditions after preparation. Obtain these details from the supplier before laboratory use.

Research Use Only

Supplied as a dry lyophilized powder. Research supplies, including Reconstitution Solution, are sold separately.

This product is not supplied as an FDA-approved medication. It is intended strictly for laboratory, analytical, and scientific research purposes. It is not intended for human or veterinary use, consumption, administration, diagnosis, prevention, or therapeutic application.

Frequently Asked Questions About Glow Blend

What is UPB Glow Blend?

UPB Glow Blend is a laboratory research product combining BPC-157, TB-500, and GHK-Cu in one lyophilized formulation.

How much of each component is listed per vial?

Each vial is labeled with BPC-157 10 mg, TB-500 10 mg, and GHK-Cu 50 mg. The total labeled content is 70 mg.

What purity does the Glow Blend COA report?

The report for lot 11020-005 lists 99.71% purity by HPLC-UV. This is the reported blend result, not a separate purity measurement for each component.

Why do the COA measurements differ from the labeled quantities?

Labeled quantities describe the product specification. The COA records laboratory measurements from two submitted vials. Those sample-specific measurements do not change the labeled quantities or guarantee identical results for every vial.

Does Glow Blend have endotoxin and microbial test results?

Yes. The supplied COA records passing endotoxin results for two replicates and no detectable microbial DNA in the reported PCR assay. These results do not establish sterility.

How can I check the Glow Blend COA?

Open the linked report and compare lot 11020-005 with the vial label. The report’s accession number is 2607170627, and its search code is Ultr2607170627.

Is Glow Blend intended for human or veterinary use?

No. This product is supplied exclusively for laboratory, analytical, and scientific research.