FluxMPS™ Dulbecco’s Modified Eagle Medium (DMEM), High Glucose w/o L-Glutamine, Phenol Red: 1X Liquid

Product#: DCP-DMEM-QR1X
$44.00
DCP-DMEM-QR1X
Availability:
Ships in 1-2 Weeks

warning For Research Use Only (RUO). Not intended for clinical, diagnostic, or therapeutic use in humans.
verified ISO 13485 Certified Manufacturing

FluxMPS™ Dulbecco’s Modified Eagle Medium (DMEM), High Glucose w/o L-Glutamine, Phenol Red: 1X Liquid

Contains Sodium Bicarbonate Contains Calcium Contains Magnesium Contains Glucose Contains Sodium Pyruvate Without L-Glutamine Without Phenol Red

FluxMPS™ DCP-DMEM-QR1X is a Microfluidics Suitable, quadruple-stage ultra-filtered (0.1 µm ×2 + 0.04 µm ×2) DMEM High Glucose (4.5 g/L) formulation engineered for organ-on-a-chip (OoC), microphysiological systems (MPS), and energy-demanding cell models. 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. Formulation: [+] High Glucose (4500 mg/L), [+] Sodium Pyruvate, [+] Sodium Bicarbonate | [-] L-Glutamine, [-] Phenol Red.

  • High Glucose (4.5 g/L) — supports energy-demanding cell types: primary neurons, cardiomyocytes, cancer lines
  • 0.04 µm final filtration — ultra-low particulate baseline for microfluidic channels below 100 µm
  • Quadruple-stage filtration: 0.1 µm Prefiltration I → 0.04 µm Final filtration I → 0.1 µm Prefiltration II → 0.04 µm Final filtration II — Polish
  • Endotoxin < 0.05 EU/mL (LAL, USP <85>), controlled per manufacturing batch
  • Formulation: [+] High Glucose (4500 mg/L), [+] Sodium Pyruvate, [+] Sodium Bicarbonate | [-] L-Glutamine, [-] Phenol Red
  • Ultrapure Type 1 water (18.2 MΩ·cm); ISO 13485:2016 QMS; ISO Class 5 aseptic fill
  • Bicarbonate-buffered (3700 mg/L NaHCO₃) — requires approximately 9.6% CO₂ to maintain pH 7.4
  • Custom pH, salts, glucose concentration, and nutrient adjustments available on request
CAT. NO.
DCP-DMEM-QR1X | Cell Culture Media UNSPSC: 41116155 | Commodity: Molecular biology and cell culture growth media | (UNv260801)
Dulbecco’s Modified Eagle Medium (DMEM), High Glucose w/o L-Glutamine, Phenol Red: 1X Liquid
  • Glucose4500 mg/L (4.5 g/L, High Glucose)
  • Formulation[+] High Glucose, [+] Sodium Pyruvate, [+] Sodium Bicarbonate, [-] L-Glutamine, [-] Phenol Red
  • AppearanceColorless to pale straw, clear solution (phenol red-free)
  • pH (USP <791>)7.4
  • Osmolality (USP <785>)320–360 mOsm/kg H2O
  • Endotoxin (USP <85>)< 0.05 EU/mL
  • Sterility (USP <71>)No growth / 14 days
  • Filtration0.1 µm ×2 + 0.04 µm ×2 (Quadruple-stage)
  • Storage2–8°C, protect from light
  • Shelf Life12 months from date of manufacture, unopened
ISO 13485:2016 USP <85> <785> <788> RUO
Why FluxMPS™

Engineered where standard media fails

Conventional 0.22 µm–filtered DMEM passes mycoplasma-sized organisms, subvisible particulates, and aggregate fragments that clog microfluidic channels and corrupt sensor signals. FluxMPS™ High Glucose reduces these failure modes while delivering 4.5 g/L glucose for energy-demanding cell types and complex tissue models.

filter_alt

Microchannel-safe purity

0.04 µm final filtration; USP <788> Method 1 particulate compliance supports safe perfusion in sub-100 µm chip geometries.

bolt

High-energy cell support

4.5 g/L glucose (4× vs. low-glucose DMEM) sustains primary neurons, cardiomyocytes, cancer lines, and other aerobically active cells in prolonged perfusion.

water_drop

Ultrapure-grade water

Ultrapure Type 1 water (18.2 MΩ·cm) with controlled trace-metal and total organic carbon (TOC) content, minimizing feedwater-derived contaminants in the finished medium.

visibility

Low background for imaging

Ultra-low particulate baseline from 0.04 µm final filtration supports confocal microscopy and biosensor platforms; this formulation does not include phenol red.

science

Rich, stable nutrient profile

32 ingredients verified per lot; 4× BME amino acid/vitamin concentration; micro-batch production with full traceability.

tune

Customization on demand

pH, glucose, salts, HEPES, and nutrients adjustable. Contact support@diagnocine.com.

Purity Architecture

Quadruple-stage filtration system

Four serial filtration stages — two dedicated 0.1 µm/0.04 µm prefilter-and-final-filter pairs in series — reaching a final 0.04 µm polish, giving full redundancy and an ultra-low particulate baseline unavailable from conventional 0.22 µm filtered media.

  1. 1

    0.1 µm Prefiltration I — Large Particulate Removal

    Removes large aggregates, cell debris and protein clusters; protects the first 0.04 µm cartridge from early fouling.

  2. 2

    0.04 µm Final filtration I — Mycoplasma-Retentive Filtration

    First 0.04 µm pass; retains particulates and organisms in the 0.2–0.3 µm mycoplasma size range that pass a conventional 0.22 µm filter.

  3. 3

    0.1 µm Prefiltration II

    Second dedicated prefilter, protecting the second 0.04 µm cartridge and providing full redundancy across the train.

  4. 4

    0.04 µm Final filtration II — Polish

    Ultimate 0.04 µm polishing filter; aseptic fill and finish under validated conditions.

Performance vs. conventional media

5×
Cleaner than 0.22 µm media by particulate count
0.04
µm Final pore size — four-stage train
Sterility & Mycoplasma: No growth after 14-day incubation (USP <71>). Mycoplasma risk is controlled by 0.1 µm and 0.04 µm mycoplasma-retentive filtration at every production stage (not tested per lot).
Grade: This product is Microfluidics Suitable, filtered to a 0.04 µm final cut-off. It is not an MPS Grade product — that designation is reserved for the 0.01 µm ultra nano-filtered line, which adds 0.02 µm and 0.01 µm stages after the 0.04 µm polish. For applications requiring the 0.01 µm cut-off, contact support@diagnocine.com.
FluxMPS™ DCP-DMEM-QR1X Dulbecco's Modified Eagle Medium (DMEM), High Glucose w/o L-Glutamine, Phenol Red: 1X Liquid ? Quadruple-stage filtration system: 0.1 μm Prefiltration I, 0.04 μm Final filtration I, 0.1 μm Prefiltration II, 0.04 μm Final filtration II Polish ? Microfluidics Suitable DMEM High Glucose for organ-on-a-chip | Diagnocine
Figure 1. FluxMPS™ Quadruple-stage filtration system (0.1 µm ×2 + 0.04 µm ×2) for ultra-low particulate purity.
© Diagnocine® — DCP-DMEM-QR1X
Applications

Designed for next-generation cell models

FluxMPS™ DCP-DMEM-QR1X supports demanding platforms from single-channel microfluidic chips to multi-organ body-on-a-chip systems. High glucose (4.5 g/L) makes it particularly suited to energy-intensive cell types and aerobically active cultures. Available pack sizes: 500 mL, 1000 mL.

Automated Bioreactors & Robotics

Next-Generation System Uptime

Optional 0.01 µm (10 nm) MPS Grade variant available on request for automated bioreactor perfusion and robotic liquid handlers — a separate, six-stage ultra nano-filtered line distinct from this Microfluidics Suitable product.

  • Total Particulate Exclusion: 10 nm filtration removes nanoparticulate aggregates
  • Valve & Sensor Protection: Reduces micro-fouling of solenoid valves and optical sensors
  • Extended Perfusion Stability: Consistent high-glucose delivery over weeks-long culture

Inquiry Required: Contact support@diagnocine.com for the 0.01 µm MPS Grade variant.

Microfluidics

Organ-on-a-Chip & MPS

Ultra-clean 0.04 µm–filtered media reduces the risk of microchannel clogging in complex multi-organ chip architectures.

OoCToCBoCLoCMPS
Cancer Biology

Warburg Effect & Cancer Models

High glucose (4.5 g/L) supports aerobic glycolysis phenotyping in cancer cell lines requiring elevated energy substrates.

MCF-7MDA-MB-231HeLaA549
Neuroscience

Primary Neurons & Brain-on-Chip

High glucose supports the metabolic demands of primary neurons and iPSC-derived neuronal networks in microfluidic perfusion.

iPSC-NeuronsPrimary neuronsBrain-on-chip
Cardiac Biology

Cardiomyocyte & Heart-on-Chip

High-glucose DMEM is a standard base for iPSC-derived cardiomyocyte maturation and heart-on-chip functional assays.

iPSC-CMHeart-on-chipTEER
Metabolomics

Metabolic Flux Analysis

Defined high-glucose formulation supports ¹³C isotope tracing and NMR-based glycolysis/OXPHOS profiling. Not compatible with Agilent Seahorse XF assays, which require bicarbonate-free, phenol red-free medium.

¹³C tracingNMR metabolomicsGlycolysis profiling
Live-Cell Imaging

Microscopy & Optical Sensing

Ultra-low particulate baseline for confocal microscopy and biosensor platforms; formulated without phenol red.

ConfocalBiosensorsTEER
Technical Specifications

Analytical release specifications

Every lot released against the full specification matrix. CoA: support@diagnocine.com.

Physical & Chemical Parameters
Parameter Specification
Formulation [+] Sodium Bicarbonate, [+] Calcium, [+] Magnesium, [+] High Glucose (4500 mg/L), [+] Sodium Pyruvate | [-] L-Glutamine, [-] Phenol Red
Appearance Colorless to pale straw, clear solution (phenol red-free)
Glucose 4500 mg/L (4.5 g/L, High Glucose)
pH USP <791> 7.4
Osmolality USP <785> 320–360 mOsm/kg H2O
Total ingredients 32
Sterility, Purity & Safety
Parameter Specification
Endotoxin USP <85> BET < 0.05 EU/mL
Sterility USP <71> No growth / 14 days
Mycoplasma 0.1 µm & 0.04 µm mycoplasma-retentive filtration (not tested per lot)
Particulate ≥10 µm USP <788> Method 1 NMT 25/mL
Particulate ≥25 µm USP <788> Method 1 NMT 3/mL
Water purity Type 1, 18.2 MΩ·cm
Manufacturing std. ISO 13485:2016
Fill environment ISO Class 5 (Class 100)
Storage, Handling & Logistics
Parameter Specification
Storage temperature 2–8°C, protect from light
Freeze-thaw Do not freeze
Shelf life 12 months from date of manufacture, unopened
Shipping condition Cold pack
CO2 requirement Approximately 9.6% CO2 (calculated from 3700 mg/L sodium bicarbonate at pH 7.4)
Raw Materials & Regulatory
Parameter Specification
Raw material grade Reagent / cell culture grade
Traceability Full lot traceability per ISO 13485
Manufacturing QMS ISO 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, per-lot QC release
Intended use Research Use Only (RUO)
Formulation

Full composition (mg/L)

DMEM High Glucose is a modification of Basal Medium Eagle (BME) with 4× BME amino acid and vitamin concentrations, plus glycine, serine, and ferric nitrate. 32 ingredients verified per lot with CAS numbers for full raw-material traceability.

Component CAS Number mg/L
INORGANIC SALTS
Calcium chloride dihydrate 10035-04-8 265.000
Ferric nitrate nonahydrate 7782-61-8 0.100
Magnesium sulfate anhydrous 7487-88-9 97.720
Potassium chloride 7447-40-7 400.000
Sodium bicarbonate 144-55-8 3700.000
Sodium chloride 7647-14-5 6400.00
Sodium dihydrogen phosphate anhydrous 7558-80-7 109.000
Component CAS Number mg/L
AMINO ACIDS
Glycine 56-40-6 30.000
L-Arginine hydrochloride 1119-34-2 84.000
L-Cystine dihydrochloride 30925-07-6 62.570
L-Histidine hydrochloride monohydrate 5934-29-2 584.000
L-Isoleucine 73-32-5 42.000
L-Leucine 61-90-5 105.000
L-Lysine hydrochloride 657-27-2 105.000
L-Methionine 63-68-3 146.000
L-Phenylalanine 63-91-2 30.000
L-Phenylalanine 63-91-2 66.000
L-Serine 56-45-1 42.000
L-Threonine 72-19-5 95.000
L-Tryptophan 73-22-3 16.000
L-Tyrosine Disodium Salt dihydrate 69847-15-0 103.790
L-Valine 72-18-4 94.000
Component CAS Number mg/L
VITAMINS
Choline chloride 67-48-1 4.000
D-Ca-Pantothenate 137-08-6 4.000
Folic acid 59-30-3 4.000
Nicotinamide 98-92-0 4.000
Pyridoxal hydrochloride 65-22-5 4.000
Riboflavin 83-88-5 0.400
Thiamine hydrochloride 67-03-8 4.000
i-Inositol 87-89-8 7.200
OTHERS
D-Glucose 50-99-7 4500.000
Sodium pyruvate 113-24-6 110.000
Custom formulation: Contact support@diagnocine.com for DCP-DMEM-QR1X custom specifications — pH, glucose, salts, HEPES, or nutrient modifications.
Quality Assurance

Manufacturing & compliance

Every FluxMPS™ product is manufactured and released under a rigorous multi-layer quality system spanning raw materials, in-process controls, and final-product testing.

verified

ISO 13485:2016 Quality Management

Manufactured under ISO 13485:2016-certified facilities. Final QA and testing at Diagnocine R&D Center, Totowa, NJ, USA.

water_drop

Ultrapure Type 1 Water

18.2 MΩ·cm resistivity with controlled trace-metal and TOC content, supporting consistent formulation performance.

biotech

ISO Class 5 Fill & Finish

Aseptic fill in validated ISO Class 5 (Class 100) laminar-flow workstations, supporting container-closure integrity.

assignment

Micro-Batch Precision

Small-batch production, full per-lot traceability, Certificate of Analysis for every lot — no blending, no averaged QC results.

Batch-level quality control. Endotoxin is controlled per manufacturing batch rather than per unit. Every batch is tested before release and must meet the release specification:
  • 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
A Certificate of Analysis is available on request.

Endotoxin — USP <85> BET

LAL assay; release specification: < 0.05 EU/mL per manufacturing batch.

Particulate — USP <788> Method 1

Light obscuration: NMT 25/mL (≥10 µm), NMT 3/mL (≥25 µm).

Osmolality — USP <785>

Freezing-point osmometry. Target: 320–360 mOsm/kg H2O.

Documentation & CoA

Full CoA with raw-material traceability available for every lot on request.

Certificate of Analysis: Request for any DCP-DMEM-QR1X lot at support@diagnocine.com.
Product Comparison

How DCP-DMEM-QR1X compares

FluxMPS™ DCP-DMEM-QR1X vs. conventional 0.22 µm–filtered DMEM High Glucose formulations.

Parameter DCP-DMEM-QR1X (FluxMPS™) Conventional DMEM HG
(0.22 µm filtered)
Standard Alt. DMEM HG
(0.22 µm filtered)
Grade Microfluidics Suitable (0.04 µm final) Not specified (0.22 µm filtered) Not specified (0.22 µm filtered)
High Glucose DMEM without L-Glutamine and Phenol Red — imaging-clean with researcher-defined nitrogen check_circle Yes cancel No cancel No
Final filtration pore size 0.04 µm 0.22 µm 0.22 µm
Number of filtration stages 4 (Quadruple) 1 1
Mycoplasma-retentive filtration check_circle Yes (0.04 µm) cancel No cancel No
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 <788> Method 1 particulate tested check_circle Yes cancel No cancel No
Water quality Type 1, 18.2 MΩ·cm Purified water Purified water
Manufacturing QMS ISO 13485:2016 ISO 9001 or none ISO 9001 or none
Microfluidic channel compatibility check_circle Microfluidics Suitable cancel Risk of clogging cancel Risk of clogging
Custom formulation check_circle Available cancel Fixed cancel Fixed

Comparison figures from published supplier specifications, accessed 2026-09-02. Suppliers that publish no numeric endotoxin specification are shown as "Not specified".

FAQ

Frequently asked questions

Common questions about FluxMPS™ DCP-DMEM-QR1X DMEM High Glucose.

Yes. DCP-DMEM-QR1X is processed through a Quadruple-stage filtration system reaching 0.04 µm, delivering an ultra-low particulate baseline for MPS, OoC, ToC, and LoC platforms. High glucose (4.5 g/L) makes it well suited to energy-demanding cell types including primary neurons, cardiomyocytes, and cancer cell lines in long-duration chip perfusion.
 
Phenol red is removed to eliminate its weak estrogen-receptor agonist activity and reduce optical background for imaging. L-glutamine is removed for fresh supplementation (typically 2 mM at time of use), preventing degradation artefacts in long-duration perfusion. Together these create a clean optical and hormonal baseline for live-cell imaging OoC platforms.
This formulation contains 3700 mg/L sodium bicarbonate. Using the Henderson-Hasselbalch equation, maintaining pH 7.4 at this bicarbonate concentration requires approximately 9.6% CO₂, not the 5% CO₂ associated with lower-bicarbonate DMEM formulations. Verify equilibration for your specific incubator setup, or contact support@diagnocine.com for a HEPES-buffered alternative.
Yes. Add FBS (typically 5–10%), serum-free supplements, growth factors, antibiotics, or custom nutrients as required. Filter serum-containing additions through a 0.2 µm low-protein-binding PES or PVDF membrane — a 0.04 µm membrane is not suitable for serum, as it retains IgM, lipoproteins, and other large serum components. Contact support@diagnocine.com for custom co-formulation.
Every manufacturing batch is tested by LAL assay (USP <85>) before release and must meet the release specification of less than 0.05 EU/mL. See the product comparison table above for how this compares to other suppliers' published specifications.
Yes. A full CoA per lot covers: appearance, pH (USP <791>), osmolality (USP <785>), sterility (USP <71>), endotoxin (USP <85>), mycoplasma-retentive filtration status, particulate count (USP <788> Method 1), and raw-material traceability. Request at support@diagnocine.com.
Scientific References

Supporting literature

Key peer-reviewed publications supporting Microfluidics Suitable, ultra-filtered DMEM High Glucose in organ-on-a-chip and metabolic research.

  1. Huh D, et al. Reconstituting organ-level lung functions on a chip. Science. 2010;328:1662–1668. doi:10.1126/science.1188302
  2. Bhatia SN, Ingber DE. Microfluidic organs-on-chips. Nat Biotechnol. 2014;32:760–772. doi:10.1038/nbt.2989
  3. Warburg O. On the origin of cancer cells. Science. 1956;123:309–314. doi:10.1126/science.123.3191.309
  4. Novak R, et al. Robotic fluidic coupling and interrogation of multiple vascularized organ chips. Nat Biomed Eng. 2020;4:407–420. doi:10.1038/s41551-019-0497-x
  5. Katt ME, et al. In vitro tumor models: advantages, disadvantages, variables, and selecting the right platform. Front Bioeng Biotechnol. 2016;4:12. doi:10.3389/fbioe.2016.00012
  6. Jang KJ, et al. Human kidney proximal tubule-on-a-chip for drug transport and nephrotoxicity assessment. Integr Biol. 2013;5:1119–1129. doi:10.1039/c3ib40049b
  7. Schimek K, et al. Integrating biological vasculature into a multi-organ-chip microsystem. Lab Chip. 2013;13:3588–3598. doi:10.1039/c3lc50217a
  8. Luni C, et al. High-efficiency cellular reprogramming with microfluidics. Nat Methods. 2016;13:446–452. doi:10.1038/nmeth.3832
  9. Sung JH, et al. Microfabricated mammalian organ systems and their integration into models of whole animals and humans. Lab Chip. 2013;13:1201–1212. doi:10.1039/c3lc41017j

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