Demonstration Record

Analytical values shown in this experience are illustrative sample data for portal demonstration purposes only.

Lumen Therapeutics

Lumen MOTS-c Core

Lyophilized 5mg Vial

Lot

LOT-13-0242

Batch

B-1051

Released

May 15, 2026

EA Sample

ETH-01051

TrueView Certified & Independently Tested

Unit purchased by TrueView. See the nine point panel →

Independently Lab Tested

ISO/IEC 17025 accredited

Results Available

Report published

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Quantitation

MOTS-c

97.2

of label claim

Label claim:

5.00

· Detected:

4.86

Detected

4.86

Label claim

5.00

97.2

Label claim achieved

Purity

97.8

Tests Passed

Overall

Passed

Identity

Confirmed

Peptide identity

Method:

USP <621>

Specification:

Matches reference standard

Confirmed

Purity

Passed

Chromatographic Purity

Method:

HPLC

Specification:

≥ 98.5%

97.8

Pass

Quantity / Quantitation

1 analyte verified

Quantitation

MOTS-c

97.2

of label claim

Label claim:

5.00

· Detected:

4.86

Detected

4.86

Label claim

5.00

97.2

Label claim achieved

Bacterial Endotoxins

Passed

Bacterial Endotoxins

Method:

Gel-clot LAL (USP <85>)

Specification:

≤ 10 EU/mg

0.5 EU/mg

Pass

Residual Solvents

Passed

Residual solvents (GC)

Method:

USP <467>

Specification:

≤ ICH Q3C limits

< LOD ppm

Pass

Heavy Metals

4/4 passed

Arsenic (As)

4.7%

0.07 mcg/g

1.5 mcg/g

Cadmium (Cd)

4.7%

0.07 mcg/g

0.5 mcg/g

Lead (Pb)

4.7%

0.12 mcg/g

1 mcg/g

Mercury (Hg)

4.7%

0.07 mcg/g

1.5 mcg/g

[{"analyte":"Arsenic (As)","result":"0.469 mcg/g","limit":"≤ 1.5 mcg/g","status":"pass"},{"analyte":"Cadmium (Cd)","result":"0.260 mcg/g","limit":"≤ 0.5 mcg/g","status":"pass"},{"analyte":"Lead (Pb)","result":"0.652 mcg/g","limit":"≤ 1.0 mcg/g","status":"pass"},{"analyte":"Mercury (Hg)","result":"0.365 mcg/g","limit":"≤ 1.5 mcg/g","status":"pass"}]

Microbiology

Passed

Microbiological analysis

Method:

USP <61> / <62>

1/1 Passed

Pass

Sterility

Passed

Rapid sterility

Method:

Rapid sterility qPCR (USP <1223>)

Specification:

No growth at 14 days

Pass

Fentanyl

Passed

Fentanyl screen

Method:

USP <2251>

Specification:

Not detected

Not Detected

Pass

Ethos Analytics

Certificate of Analysis

Original Laboratory Report

SAMPLE REPORT — For demonstration only

Ethos Analytics

Independent analytical laboratory, Phoenix Arizona

Phoenix, AZ

ISO/IEC 17025

EA Sample ID

ETH-01051

Batch / Lot

LOT-13-0242

Date Received

May 6, 2026

Date Completed

May 15, 2026

Standard

ISO/IEC 17025:2017

Laboratory

Ethos Analytics

Phoenix, AZ

Analysis Summary

Identity

USP <621>

Pass

Purity

HPLC

Pass

Quantity

HPLC

Pass

Endotoxin

Gel-clot LAL (USP <85>)

Pass

Residual Solvents

USP <467>

Pass

Heavy Metals

ICP-MS (USP <233>)

Pass

Microbiology

USP <61> / <62>

Pass

Sterility

Rapid sterility qPCR (USP <1223>)

Pass

Fentanyl

USP <2251>

Pass

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