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

Product#: DCP-DMEM-GQR1X
$44.00
DCP-DMEM-GQR1X
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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) w/o Glucose, L-Glutamine, Phenol Red: 1X Liquid

Contains Sodium BicarbonateContains CalciumContains MagnesiumContains Sodium PyruvateWithout L-GlutamineWithout Phenol RedWithout Glucose

Microfluidics Suitable, quadruple-stage ultra-filtered (0.1 µm ×2 + 0.04 µm ×2) 1X liquid cell culture medium engineered for microfluidic channels, organ-on-a-chip (OoC), and microphysiological systems (MPS). Manufactured under ISO 13485:2016 in an ISO Class 5 fill environment using Ultrapure Type 1 water (18.2 MΩ·cm).

  • Quadruple-stage filtration to a 0.04 µm final pore size (0.1 µm ×2 + 0.04 µm ×2)
  • Endotoxin release specification: < 0.05 EU/mL (USP <85> BET, LAL assay)
  • Formulated without glucose, L-glutamine and phenol red; contains 110 mg/L sodium pyruvate for defined metabolic control
  • 3700 mg/L sodium bicarbonate buffering system — requires a 10% CO₂ incubator to maintain pH 7.4
  • Manufactured under an ISO 13485:2016 quality management system in an ISO Class 5 fill environment
  • Prepared with Ultrapure Type 1 water (18.2 MΩ·cm)
  • Custom pH, glucose, HEPES, salts & nutrients available — support@diagnocine.com
DCP-DMEM-GQR1X · Cell Culture Media UNSPSC: 41116155 | Commodity: Molecular biology and cell culture growth media | (UNv260801)
Dulbecco's Modified Eagle Medium (DMEM) w/o Glucose, L-Glutamine, Phenol Red: 1X Liquid
  • GlucoseNot added
  • L-GlutamineNot added ([-])
  • Sodium Pyruvate110 mg/L ([+])
  • pH (USP <791>)7.4
  • Osmolality (USP <785>)310 - 350 mOsm/kg
  • Endotoxin (USP <85>)< 0.05 EU/mL
  • Filtration0.1µm ×2 + 0.04µm ×2
  • Storage2-8°C, protect from light
  • Shelf Life12 months from date of manufacture, unopened
  • ShippingCold pack (2–8°C)
ISO 13485:2016 USP <85> <785> <788> RUO
Why FluxMPS™

Engineered where standard media fails

Conventional 0.22 µm filtered media allows mycoplasma (0.2–0.3 µm), sub-visible particulates, and microaggregates to pass freely — clogging microchannels, corrupting biosensors, and invalidating metabolic assays. FluxMPS™ closes that gap.

filter_alt

Microchannel-safe purity

0.04 µm final filter targets fine particulates that pass a standard 0.22 µm filter, supporting unobstructed flow in narrow microfluidic channels.

target

Total metabolic control

A defined carbon-source profile enables Warburg-effect studies, glycolysis inhibition, and ¹³C metabolic tracing.

water_drop

Ultrapure-grade water

Prepared with Ultrapure Type 1 water (18.2 MΩ·cm) — low trace-metal and organic-carbon (TOC) content for consistent performance in sensitive assays.

visibility

Low background for imaging

Low particulate baseline supports confocal live-cell imaging, fluorescent biosensors, and automated high-content analysis on chip.

science

Rich, stable nutrient profile

4× BME amino acid and vitamin concentrations with micro-batch precision — tight lot-to-lot consistency for long-duration MPS perfusion.

tune

Customization on demand

pH, glucose, HEPES, salts, and nutrients adjusted on request. Contact support@diagnocine.com.

Purity Architecture

Quadruple-stage filtration system

This 1X liquid cell culture medium undergoes a validated four-stage sequential filtration reaching a final pore size of 0.04 µm — capturing sub-micron particulates and bioburden that standard 0.22 µm filtration misses entirely.

  1. 1

    0.1 µm Prefiltration I

    Removes large particulates, cell debris, and protein aggregates. Protects the first 0.04 µm final filter cartridge.

  2. 2

    0.04 µm Final filtration I

    First 0.04 µm pass; retains sub-micron particulates and microaggregates that pass a 0.22 µm filter.

  3. 3

    0.1 µm Prefiltration II

    Second dedicated prefilter, protecting the second 0.04 µm final filter cartridge.

  4. 4

    0.04 µm Final filtration II — Polish

    Ultimate polishing filter; aseptic fill in a validated ISO Class 5 (Class 100) laminar-flow workstation.

Performance vs. conventional media

FluxMPS™ media are produced through a validated 0.04 µm final filtration pathway assessed by USP <788> Method 1 (light obscuration) — supporting long-duration perfusion where standard 0.22 µm media risk channel occlusion.

4
Sequential filtration passes (0.1 µm ×2 + 0.04 µm ×2)
0.04
µm Final filter — sub-mycoplasma polishing
Sterility & Mycoplasma: 14-day USP <71> sterility tested per lot. The 0.1 µm stages provide mycoplasma-retentive filtration (mycoplasma diameter 0.2–0.3 µm) but are not a substitute for lot-specific mycoplasma testing (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™ Dulbecco's Modified Eagle Medium (DMEM) w/o Glucose, L-Glutamine, Phenol Red: 1X Liquid (DCP-DMEM-GQR1X) ? Quadruple-stage filtration system (0.1 μm ×2 + 0.04 μm ×2) for organ-on-a-chip and microfluidic MPS cell culture | Diagnocine
Figure 1. FluxMPS™ Quadruple-stage filtration: 0.1µm Prefiltration I → 0.04µm Final filtration I → 0.1µm Prefiltration II → 0.04µm Final filtration II (Polish) → ISO Class 5 aseptic fill.
© Diagnocine® — DCP-DMEM-GQR1X
Applications

Optimized for next-generation cell biology platforms

FluxMPS™ Dulbecco's Modified Eagle Medium (DMEM) w/o Glucose, L-Glutamine, Phenol Red: 1X Liquid is validated for applications where microchannel cleanliness, signal fidelity, and metabolic precision are critical.

Automated Bioreactors & Robotics

Next-Generation System Uptime

For fully automated bioreactor and robotic liquid-handling platforms, Diagnocine offers an optional 0.01 µm (10 nm) ultra nano-filtered MPS Grade variant of this formulation, engineered to protect precision valves, sensors, and long-duration perfusion loops.

  • Total Particulate Exclusion — six-stage cascade down to 0.01 µm
  • Valve & Sensor Protection — minimizes fouling in automated fluidics
  • Extended Perfusion Stability — supports multi-week continuous-flow runs

Inquiry Required: The 0.01 µm MPS Grade variant is available on request — contact support@diagnocine.com.

Microfluidics

Micro Physiological System (MPS) & Chip

Low-particulate, filtration-controlled media for perfusion in organ chips, tissue chips (ToC), and body-on-a-chip (BoC) devices.

OoCToCBoCMPS
Cancer Biology

Warburg Effect & Metabolic Research

Glucose-free formulation with a defined pyruvate carbon source for Warburg-effect studies, aerobic glycolysis, and cancer metabolomics.

MCF-7MDA-MB-231HeLaA549
Stem Cell Biology

iPSC-Derived Models

Low-endotoxin, low-particulate baseline for use in iPSC differentiation and functional organoid readouts, supplemented per protocol.

iPSC-NeuronsiPSC-CMiPSC-Hep
Vascular Biology

Endothelial & Primary Cells

Filtration-controlled perfusion media for TEER measurement, endothelial monolayer integrity, and primary cell culture.

HUVECsHAECsPrimary hepatocytes
Metabolomics

Metabolic Flux Analysis

Chemically defined formulation for ¹³C metabolic tracing and NMR metabolomics. Not compatible with Agilent Seahorse XF assays, which require bicarbonate-free, phenol red-free medium.

¹³C tracingNMR
Live-Cell Imaging

Microscopy & Optical Sensing

Low particulate baseline for confocal microscopy, fluorescent biosensors, and automated imaging on chip.

ConfocalBiosensorsTEER
Technical Specifications

Full technical specification

Every lot of FluxMPS™ Dulbecco's Modified Eagle Medium (DMEM) w/o Glucose, L-Glutamine, Phenol Red: 1X Liquid is released against comprehensive multi-parameter QC specifications.

Physical & Chemical Parameters
Parameter Specification
Formulation [+] Sodium Bicarbonate, Calcium, Magnesium, Sodium Pyruvate / [-] Glucose, L-Glutamine, Phenol Red
Appearance Colorless to pale yellow, clear solution
pH USP <791> 7.4
Osmolality USP <785> 310 - 350 mOsm/kg H₂O
Glucose Not added
L-Glutamine Not added
Sodium Pyruvate 110 mg/L
Phenol Red Not added
Sterility, Purity & Safety Parameters
Parameter Specification
Endotoxin USP <85> BET < 0.05 EU/mL
Sterility USP <71> No growth after 14 days
Mycoplasma 0.1 µm mycoplasma-retentive filtration (not tested per lot)
Water purity Ultrapure Type 1, 18.2 MΩ·cm
Manufacturing ISO 13485:2016 ISO
Fill environment ISO Class 5 (Class 100)
Storage, Handling & Logistics
Parameter Specification
Storage 2-8°C, protect from light
Freeze–thaw Do not freeze
Shelf life 12 months from date of manufacture, unopened
Shipping Cold pack (2–8°C)
CO₂ requirement 10% CO₂ incubator required
Raw Materials & Regulatory Traceability
Parameter Specification
Raw material grade Pharmaceutical/research grade CoA
Manufacturing QMS ISO 13485:2016 ISO
UNSPSC 41116155 — Molecular biology and cell culture growth media (UNv260801)
Regulatory 21 CFR Part 820 (QMSR) aligned
Production Micro-batch; Totowa, NJ, USA
Pack sizes 500 mL, 1000 mL
Intended use RUO only
Formulation

Full composition (mg/L)

Every ingredient below is present in this 1X liquid formulation at the exact concentration listed. Total: 31 components across 4 categories. All values are per-lot verified and reported on the Certificate of Analysis (CoA).

INORGANIC SALTS

Component CAS Number mg/L
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 6400.000
Sodium dihydrogen phosphate anhydrous 7558-80-7 109.000

AMINO ACIDS

Component CAS Number mg/L
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 69847-45-6 103.790
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
OTHERS
i-Inositol 87-89-8 7.200
Sodium pyruvate 113-24-6 110.000
Custom formulations: pH, glucose, HEPES, salts, and individual nutrient levels adjustable on request. Contact support@diagnocine.com.
Quality Assurance

Manufacturing & compliance

Every batch subjected to multi-parameter lot-release testing before distribution.

verified

ISO 13485:2016 QMS

Manufactured by ISO 13485-certified suppliers. Final packaging, QA and testing at DiagnoCine R&D Center; customization at DiagnoCine Precision, Totowa, NJ, USA.

water_drop

Ultrapure Type 1 Water

Prepared using Ultrapure Type 1 water (18.2 MΩ·cm) with low trace-metal and total organic carbon (TOC) content, supporting consistent performance in sensitive biosensor and imaging workflows.

biotech

ISO Class 5 Fill & Finish

Validated ISO Class 5 laminar-flow workstation with real-time particle monitoring. Preserves filtration integrity through final fill.

assignment

Micro-Batch Precision

Small-batch production for tight lot-to-lot consistency across pH, osmolality, and endotoxin — critical for reproducible long-duration MPS experiments.

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. Assay sensitivity: 0.005 EU/mL. Tested per manufacturing batch.

Sterility — USP <71>

14-day sterility test per lot; no growth observed at release.

Osmolality — USP <785>

Freezing-point depression osmometry. Release range: 310 - 350 mOsm/kg H₂O.

Certificate of Analysis (CoA)

Full CoA per lot. Request at support@diagnocine.com with lot number.

CoA Request: Available at no charge for any production lot of FluxMPS™ Dulbecco's Modified Eagle Medium (DMEM) w/o Glucose, L-Glutamine, Phenol Red: 1X Liquid (DCP-DMEM-GQR1X). Email support@diagnocine.com.
Product Comparison

How DCP-DMEM-GQR1X compares

Critical advantages in filtration, mycoplasma-retentive processing, water quality, and QC depth versus conventional 0.22 µm filtered media for MPS and microfluidic applications.

Parameter DCP-DMEM-GQR1X (FluxMPS™) Standard DMEM (0.22 µm) Competitor DMEM (0.22 µm)
Grade Microfluidics Suitable Not applicable Not applicable
Formulation definition [+] Sodium Bicarbonate, Calcium, Magnesium, Sodium Pyruvate / [-] Glucose, L-Glutamine, Phenol Red Standard Standard
Final filtration pore size 0.04 µm (40 nm) 0.22 µm 0.22 µm
Filtration stages 4 (Quadruple) 1 1
Mycoplasma-retentive filtration check_circle cancel cancel
Endotoxin (release specification) FluxMPS™ — < 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> particulate compliance check_circle Method 1 cancel cancel
Water quality Ultrapure Type 1, 18.2 MΩ·cm Unspecified Unspecified
Manufacturing QMS ISO 13485:2016 Varies Varies
Microfluidic channel compatibility check_circle cancel cancel
Custom formulation check_circle On request cancel cancel

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™ Dulbecco's Modified Eagle Medium (DMEM) w/o Glucose, L-Glutamine, Phenol Red: 1X Liquid (DCP-DMEM-GQR1X).

DCP-DMEM-GQR1X is engineered for organ-on-a-chip (OoC), microphysiological system (MPS), and microfluidic applications. Quadruple-stage filtration to a 0.04 µm final pore size, including dedicated 0.1 µm mycoplasma-retentive stages, reduces sub-micron particulates and bioburden risk that can clog microchannels in standard 0.22 µm media.
Four sequential stages (0.1 µm ×2 + 0.04 µm ×2) target mycoplasma (0.2–0.3 µm), sub-visible particulates, and bioburden not addressed by conventional 0.22 µm filtration. Compliance is assessed per USP <788> Method 1 (light obscuration).
DCP-DMEM-GQR1X is formulated without glucose to enable precise metabolic control — including Warburg-effect studies, glycolysis inhibition, and ¹³C carbon-source tracing. Add D-glucose at your desired concentration (typically 1–4.5 g/L) or substitute galactose for glycolytic flux control. Note that this formulation already contains 110 mg/L sodium pyruvate. Contact support@diagnocine.com for pre-supplemented variants.
Yes — DCP-DMEM-GQR1X contains 3700 mg/L sodium bicarbonate and requires a 10% CO₂ incubator to maintain physiological pH 7.4. For CO₂-independent use, add 10–25 mM HEPES or request the bicarbonate-free variant.
DCP-DMEM-GQR1X is a basal medium compatible with FBS (2–10%), human serum, GlutaMAX, EGF, FGF, VEGF, and antibiotics. Pre-filter serum-containing or protein-based additions through a 0.2 µm low-protein-binding PES or PVDF filter before combining to maintain Microfluidics Suitable purity.
Every batch is tested before release and must meet the release specification of < 0.05 EU/mL by USP <85> LAL assay (assay sensitivity 0.005 EU/mL). Endotoxin is controlled per manufacturing batch; lot-specific results are available on the Certificate of Analysis — request at support@diagnocine.com.
Yes — full CoA per lot includes: lot number, expiry, appearance, pH (USP <791>), osmolality (USP <785>), endotoxin (USP <85>), sterility (USP <71>), and particulate assessment (USP <788>). Email support@diagnocine.com.
Scientific References

Supporting literature

  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. Vander Heiden MG, et al. Understanding the Warburg effect. Science. 2009;324:1029–1033. doi:10.1126/science.1160809
  4. Sontheimer-Phelps A, et al. Modelling cancer in microfluidic human organs-on-chips. Nat Rev Cancer. 2019;19:65–81. doi:10.1038/s41568-018-0104-6
  5. van Duinen V, et al. Microfluidic 3D cell culture. Curr Opin Biotechnol. 2015;35:118–126. doi:10.1016/j.copbio.2015.05.002
  6. Jang KJ, et al. Reproducing human drug toxicities using a Liver-Chip. Sci Transl Med. 2019;11:eaax5516. doi:10.1126/scitranslmed.aax5516
  7. Kasendra M, et al. Primary human Small Intestine-on-a-Chip. Sci Rep. 2018;8:2871. doi:10.1038/s41598-018-21201-7
  8. Skardal A, et al. Multi-tissue organ-on-a-chip platform. Sci Rep. 2017;7:8837. doi:10.1038/s41598-017-08879-x

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