FluxMPS™ Minimum Essential Medium (MEM), High Glucose & 25mM HEPES w/o L-Glutamine: 1X Liquid
FluxMPS™ Minimum Essential Medium (MEM), High Glucose & 25mM HEPES w/o L-Glutamine: 1X Liquid
FluxMPS™ Minimum Essential Medium (MEM), High Glucose & 25mM HEPES w/o L-Glutamine: 1X Liquid is a Microfluidics Suitable, ultra-filtered cell culture medium engineered for organ-on-a-chip (OoC), tissue-on-a-chip (ToC), and microphysiological system (MPS) applications. A quadruple-stage train (0.1 µm ×2 + 0.04 µm ×2) reaches a 0.04 µm final cut-off, five times finer than the 0.22 µm membranes used for conventional sterile filtration.
- High-glucose (4.5 g/L) MEM base with 25 mM HEPES supplemental buffering and 110 mg/L sodium pyruvate — supports high-energy-demand cell types
- L-Glutamine excluded from the formulation (0 mg/L) for user-controlled, lot-to-lot supplementation
- Quadruple-stage filtration train: 0.1 µm → 0.04 µm → 0.1 µm → 0.04 µm, reaching a 0.04 µm final cut-off
- Endotoxin release specification < 0.05 EU/mL (LAL, USP <85>), controlled per manufacturing batch
- Prepared with Ultrapure Type 1 water (18.2 MΩ·cm; ASTM D1193 Type I); aseptic ISO Class 5 fill & finish
- Manufactured under an ISO 13485:2016 quality management system; final packaging and QC at Diagnocine, Totowa, NJ
- Sodium bicarbonate (2200 mg/L) present alongside HEPES buffering — compatible with standard to reduced CO₂ incubation; validate per cell line
- Custom formulations available — pH, glucose, salts, HEPES, and nutrient composition on request
- Glucose4500 mg/L (4.5 g/L)
- L-GlutamineNot added — supplement as needed
- Sodium Pyruvate110 mg/L
- HEPES5958 mg/L (25 mM)
- Sodium Bicarbonate2200 mg/L
- pH (USP <791>)7.4
- Osmolality (USP <785>)See CoA
- Endotoxin (USP <85>)< 0.05 EU/mL
- Filtration0.1 µm ×2 + 0.04 µm ×2
- Shelf Life12 months from manufacture
Engineered where standard media fails
Conventional 0.22 µm-filtered media carry mycoplasma-sized particulates (0.2–0.3 µm), subvisible debris, and batch-to-batch endotoxin variability that accumulate inside microchannels — corrupting biosensor readings and shortening device lifetimes. FluxMPS™ addresses these failure modes with a validated four-stage filtration process.
Microchannel-safe purity
0.04 µm final filter retains particulates well below the mycoplasma size range; USP <788> Method 1 particulate compliance verified per manufacturing batch.
High-glucose metabolic support
4.5 g/L glucose supports high-energy-demand cell types including HeLa, MCF-7, fibroblasts, and iPSC-derived models in perfusion devices.
Ultrapure-grade water
Prepared with Type 1 water (18.2 MΩ·cm; ASTM D1193 Type I / ISO 3696), supporting tight control of trace metals and organic carbon (TOC) in the finished medium.
Low background for imaging
Ultra-low particulate baseline supports confocal microscopy, live-cell biosensors, and TEER measurements without particulate interference.
Rich, stable nutrient profile
Complete essential amino acid profile plus micro-batch precision manufacturing ensures consistent nutrient delivery across production lots.
Customization on demand
pH, glucose, salts, HEPES, and full nutrient composition available on request. Contact support@diagnocine.com.
Quadruple-stage filtration system
FluxMPS™ Minimum Essential Medium (MEM), High Glucose & 25mM HEPES w/o L-Glutamine: 1X Liquid is processed through a four-stage filtration train — two dedicated prefilter-plus-final-filter pairs — reaching a 0.04 µm final pore size, addressing mycoplasma-sized and subvisible particulates that 0.22 µm filtration cannot remove.
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1
0.1 µm Prefiltration I
Removes large particulates, cell debris, and protein aggregates; protects the first 0.04 µm final filter cartridge.
-
2
0.04 µm Final filtration I
First 0.04 µm pass; retains sub-micron particulates and microaggregates that pass through a 0.22 µm filter.
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3
0.1 µm Prefiltration II
Second dedicated prefilter, protecting the second 0.04 µm final filter cartridge from residual particulate load.
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4
0.04 µm Final filtration II — Polish
Ultimate polishing filter; aseptic fill & finish performed in a validated ISO Class 5 laminar-flow workstation.
Performance vs. conventional media
Two sequential prefilter-plus-final-filter pairs reaching 0.04 µm deliver approximately 5× cleaner media by particulate count compared to single-pass 0.22 µm filtration, with USP <788> Method 1 compliance verified on every production batch.
© Diagnocine® — DCP-MEMGH-QN1X
Designed for next-generation cell culture platforms
FluxMPS™ Minimum Essential Medium (MEM), High Glucose & 25mM HEPES w/o L-Glutamine: 1X Liquid is suited for organ-on-a-chip, cancer biology, metabolic research, live-cell imaging, and primary cell models where particulate load and endotoxin variability must be minimized.
Automated Bioreactors & Robotics
An optional 0.01 µm (10 nm) MPS Grade ultra nano-filtered variant of this formulation is available for automated bioreactor and robotic perfusion systems requiring the highest particulate exclusion.
- Total Particulate Exclusion: 0.01 µm ultra nano-filtration for valve and sensor protection
- Valve & Sensor Protection: reduces particulate-induced blockage risk in precision fluidic systems
- Extended Perfusion Stability: supports flow-rate consistency across multi-week automated runs
Inquiry Required: Contact support@diagnocine.com to request the MPS Grade 0.01 µm variant.
Micro Physiological System (MPS) & Chip
Ultra-filtered formulation helps prevent microchannel clogging and supports laminar flow integrity across complex chip geometries.
Warburg Effect & Metabolic Research
High-glucose base supports Warburg effect studies and glucose uptake assays in cancer cell lines.
iPSC-Derived Models
Low-particulate formulation supports sensitive iPSC differentiation protocols.
Endothelial & Primary Cells
Microchannel-safe purity supports endothelial barrier integrity and TEER measurements in perfusion models.
Metabolic Flux Analysis
High-glucose base enables precise 13C isotope tracing and glycolytic flux experiments. Not compatible with Agilent Seahorse XF assays, which require bicarbonate-free, phenol red-free medium.
Microscopy & Optical Sensing
Ultra-low particulate load supports high-content confocal imaging and optical biosensor integration.
Batch-release quality parameters
Every production batch of FluxMPS™ Minimum Essential Medium (MEM), High Glucose & 25mM HEPES w/o L-Glutamine: 1X Liquid undergoes the complete quality-release battery below before shipment.
| Parameter | Specification |
|---|---|
| Formulation | + Sodium Bicarbonate, Phenol Red, HEPES, Calcium, Magnesium, Glucose, Sodium Pyruvate; − L-Glutamine |
| Appearance | Orange-to-red, clear solution (phenol red indicator present) |
| pH USP <791> | 7.4 |
| Osmolality USP <785> | See CoA |
| Glucose | 4500 mg/L (4.5 g/L) |
| L-Glutamine | Not added — supplement as needed |
| Sodium Pyruvate | 110 mg/L |
| Phenol Red | 11 mg/L (present) |
| Parameter | Specification |
|---|---|
| Endotoxin USP <85> BET | < 0.05 EU/mL (see § Manufacturing & QA for batch-release basis) |
| Sterility USP <71> | No growth after 14 days |
| Mycoplasma | 0.1 µm mycoplasma-retentive filtration (not tested per lot) |
| Particulate ≥10 µm USP <788> Method 1 | Compliant |
| Particulate ≥25 µm USP <788> Method 1 | Compliant |
| Water purity | Ultrapure Type 1 (18.2 MΩ·cm; ASTM D1193 Type I) |
| Manufacturing std. ISO 13485 | ISO 13485:2016 |
| Fill environment | ISO Class 5 (Class 100) |
| Parameter | Specification |
|---|---|
| Storage temperature | 2–8°C, protected from light |
| Freeze-thaw | Not recommended |
| Shelf life | 12 months from date of manufacture, unopened |
| Shipping condition | Cold pack |
| CO₂ requirement | HEPES-buffered (25 mM) with sodium bicarbonate (2200 mg/L) as secondary buffer; compatible with ambient-air to standard CO₂ incubation — validate per cell line |
| Parameter | Specification |
|---|---|
| Raw material grade | Cell culture / reagent grade |
| Traceability | Full batch documentation, CoA available |
| Manufacturing QMS | ISO 13485:2016 certified |
| UNSPSC | 41116155 — Molecular biology and cell culture growth media (UNv260801) |
| Regulatory alignment | 21 CFR Part 820 (QMSR) aligned |
| Production method | Micro-batch precision manufacturing |
| Intended use | For Research Use Only (RUO) |
Full composition (mg/L)
Complete formulation with CAS numbers, reproduced from manufacturer specification. Total: 30 components across 4 categories. Custom compositions available on request.
| Component | CAS Number | mg/L |
|---|---|---|
| INORGANIC SALTS | ||
| Calcium chloride dihydrate | 10035-04-8 | 265.000 |
| Magnesium sulfate anhydrous | 7487-88-9 | 97.720 |
| Potassium chloride | 7447-40-7 | 400.000 |
| Sodium bicarbonate | 144-55-8 | 2200.000 |
| Sodium chloride | 7647-14-5 | 6800.000 |
| Sodium phosphate dibasic anhydrous | 7558-79-4 | 122.000 |
| Component | CAS Number | mg/L |
|---|---|---|
| AMINO ACIDS | ||
| L-Arginine hydrochloride | 1119-34-2 | 126.000 |
| L-Cystine dihydrochloride | 30189-89-0 | 31.300 |
| L-Histidine hydrochloride monohydrate | 5934-29-2 | 42.000 |
| L-Isoleucine | 73-32-5 | 52.000 |
| L-Leucine | 61-90-5 | 52.000 |
| L-Lysine hydrochloride | 657-27-2 | 72.500 |
| L-Methionine | 63-68-3 | 15.000 |
| L-Phenylalanine | 63-91-2 | 32.000 |
| L-Threonine | 72-19-5 | 48.000 |
| L-Tryptophan | 73-22-3 | 10.000 |
| L-Tyrosine disodium salt | 69847-45-6 | 51.900 |
| L-Valine | 72-18-4 | 46.000 |
| Component | CAS Number | mg/L |
|---|---|---|
| VITAMINS | ||
| Choline chloride | 67-48-1 | 1.000 |
| D-Ca-Pantothenate | 137-08-6 | 1.000 |
| Folic acid | 59-30-3 | 1.000 |
| Niacinamide | 98-92-0 | 1.000 |
| Pyridoxine hydrochloride | 58-56-0 | 1.000 |
| Riboflavin | 83-88-5 | 0.100 |
| Thiamine hydrochloride | 67-03-8 | 1.000 |
| i-Inositol | 87-89-8 | 2.000 |
| OTHERS | ||
| D-Glucose | 50-99-7 | 4500.000 |
| HEPES | 7365-45-9 | 5958.000 |
| Phenol red sodium salt | 34487-61-1 | 11.000 |
| Sodium Pyruvate | 113-24-6 | 110.000 |
ISO 13485:2016 manufacturing & compliance
Manufactured under ISO 13485:2016 QMS with final packaging, testing, and customization at Diagnocine Precision in Totowa, New Jersey, USA.
ISO 13485:2016 QMS
Full quality management system certification covering manufacturing, testing, and release for every production batch.
Ultrapure Type 1 Water
All media prepared with 18.2 MΩ·cm resistivity water meeting ASTM D1193 Type I / ISO 3696 standards.
ISO Class 5 Fill & Finish
Aseptic filling in a validated ISO Class 5 laminar-flow workstation; 21 CFR Part 820 (QMSR) aligned.
Micro-Batch Precision
Small-batch manufacturing supports batch-to-batch nutrient consistency for reproducible perfusion studies.
Endotoxin — USP <85> BET
LAL assay performed per manufacturing batch. Release specification: < 0.05 EU/mL.
Particulate — USP <788> Method 1
Light obscuration particle count confirms ≥10 µm and ≥25 µm compliance per batch.
Osmolality — USP <785>
Freezing-point osmometry per USP <785>. Result: see Certificate of Analysis.
Documentation — CoA & Full Batch Records
Certificate of Analysis with full QC panel, traceability, and release signatures for every batch.
- Endotoxin — LAL assay, USP <85> Bacterial Endotoxins Test; assay sensitivity 0.005 EU/mL; release specification < 0.05 EU/mL
- pH, osmolality, conductivity, appearance and clarity
- Sterility
How DCP-MEMGH-QN1X (FluxMPS™) compares
Side-by-side comparison against conventional 0.22 µm-filtered MEM High Glucose alternatives, and against published supplier endotoxin specifications.
| Parameter | DCP-MEMGH-QN1X (FluxMPS™) | Conventional MEM High Glucose (0.22 µm) | Standard MEM High Glucose alternative |
|---|---|---|---|
| Grade | Microfluidics Suitable | Standard grade | Standard grade |
| Base formulation | MEM, High Glucose & 25mM HEPES w/o L-Glutamine | MEM High Glucose standard | MEM High Glucose equivalent |
| Final filtration pore size | 0.04 µm | 0.22 µm | 0.22 µm |
| Number of filtration stages | 4 stages | 1 stage | 1–2 stages |
| Mycoplasma barrier filtration | check_circle | cancel | cancel |
| Endotoxin (release specification) | < 0.05 EU/mL | Corning classical liquid media — < 0.25 EU/mL Sigma-Aldrich DMEM complete medium — ≤ 2 EU/mL Gibco classical DMEM — Not specified (recorded per lot) |
|
| USP particulate compliance | check_circle USP <788> Method 1 | cancel | cancel |
| Water quality | Ultrapure Type 1 (18.2 MΩ·cm) | Purified water | Purified water |
| Manufacturing QMS | ISO 13485:2016 | Variable | Variable |
| Microfluidic channel compatibility | check_circle Validated | cancel Clogging risk | cancel Clogging risk |
| Custom formulation | check_circle On request | cancel | Limited |
Comparison figures from published supplier specifications, accessed 2 September 2026. Suppliers that publish no numeric endotoxin specification are shown as "Not specified".
Frequently asked questions
Common questions about FluxMPS™ Minimum Essential Medium (MEM), High Glucose & 25mM HEPES w/o L-Glutamine: 1X Liquid and Microfluidics Suitable cell culture media.
Supporting literature
Peer-reviewed publications supporting Microfluidics Suitable ultra-filtered media and microfluidic cell culture applications.
- Huh D et al. (2010). Reconstituting organ-level lung functions on a chip. Science, 328(5986), 1662–1668. doi:10.1126/science.1188302
- Bhatia SN & Ingber DE (2014). Microfluidic organs-on-chips. Nature Biotechnology, 32(8), 760–772. doi:10.1038/nbt.2989
- Eagle H (1959). Amino acid metabolism in mammalian cell cultures. Science, 130(3373), 432–437. doi:10.1126/science.130.3373.432
- Warburg O (1956). On the origin of cancer cells. Science, 123(3191), 309–314. doi:10.1126/science.123.3191.309
- Bhattacharya S et al. (2018). Challenges in maintaining cell viability during microfluidic experiments. Electrophoresis, 39(7), 997–1006. doi:10.1002/elps.201700375
- Zhang YS et al. (2017). Multisensor-integrated organs-on-chips for automated in situ monitoring. PNAS, 114(12), E2293–E2302. doi:10.1073/pnas.1612906114
- Vernetti L et al. (2017). Functional coupling of human microphysiology systems. Scientific Reports, 7, 42296. doi:10.1038/srep42296
- Esch EW et al. (2015). Organs-on-chips at the frontiers of drug discovery. Nature Reviews Drug Discovery, 14(4), 248–260. doi:10.1038/nrd4539
- Zheng F et al. (2021). Organ-on-a-chip systems: microengineering to biomimic living systems. Small, 17(7), 2004175. doi:10.1002/smll.202004175
