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

Product#: DCP-DMEM-GQB1X
$34.10
DCP-DMEM-GQB1X
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) w/o Glucose, L-Glutamine, Sodium Bicarbonate: 1X Liquid

Contains Phenol Red Contains Calcium Contains Magnesium Contains Sodium Pyruvate Without L-Glutamine Without Sodium Bicarbonate Without 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). Formulated without glucose, L-glutamine, or sodium bicarbonate, with 110 mg/L sodium pyruvate retained as an alternative carbon source for defined metabolic studies.

  • Quadruple-stage filtration (0.1 µm ×2 + 0.04 µm ×2) — two dedicated prefilter/final-filter pairs for mycoplasma-size and sub-micron particulate reduction
  • Endotoxin release specification: less than 0.05 EU/mL (USP <85> BET, tested per manufacturing batch)
  • Formulated without glucose, L-glutamine and sodium bicarbonate; contains 110 mg/L sodium pyruvate as an alternative carbon source
  • Ultrapure Type 1 water (18.2 MΩ·cm) with tight trace-metal and organic-carbon control
  • Manufactured under an ISO 13485:2016 quality management system with ISO Class 5 (Class 100) aseptic fill & finish
  • 4× Basal Medium Eagle (BME) amino acid and vitamin concentrations, characteristic of the DMEM formulation
  • Custom pH, glucose, HEPES, salts & nutrients available — support@diagnocine.com
DCP-DMEM-GQB1X · 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, Sodium Bicarbonate: 1X Liquid
  • GlucoseRemoved
  • L-GlutamineRemoved ([-])
  • 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, away from bright 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 complicating metabolic assays. FluxMPS™ closes that gap.[1]

filter_alt

Microchannel-safe purity

A 0.04 µm final filtration stage, applied twice within the quadruple-stage train, supports unobstructed flow in narrow microfluidic channels.[2]

target

Total metabolic control

A defined, glucose-free carbon source with 110 mg/L sodium pyruvate supports Warburg-effect studies, glycolysis inhibition, and 13C metabolic tracing.[3]

water_drop

Ultrapure-grade water

Prepared with Ultrapure Type 1 water (18.2 MΩ·cm) under tight trace-metal and organic-carbon (TOC) control, supporting reproducible electrochemical biosensor and TEER-based assay conditions.

visibility

Low background for imaging

Ultra-low particulate baseline for 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 production — 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

FluxMPS™ applies a validated four-stage filtration train (0.1 µm ×2 + 0.04 µm ×2) reaching a final pore size of 0.04 µm, run as two dedicated prefilter/final-filter pairs to reduce sub-micron particulates and mycoplasma-size organisms beyond the reach of single-stage 0.22 µm filtration.

  1. 1

    0.1 µm Prefiltration I

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

  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.

Filtration architecture

FluxMPS™ runs two repeated prefilter/final-filter pairs in series rather than a single descending cascade: each 0.04 µm final filter is protected by its own dedicated 0.1 µm prefilter, giving full redundancy across the train.

4
Sequential filtration passes (0.1 µm ×2 + 0.04 µm ×2)
0.04
µm final filter pore size — sub-mycoplasma polishing
Sterility & Mycoplasma: 14-day USP <71> sterility testing per batch. Mycoplasma risk is mitigated by the 0.1 µm and 0.04 µm filtration stages (not tested per lot to USP <63>). Mycoplasma organisms are typically 0.2–0.3 µm in diameter.
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, Sodium Bicarbonate 1X Liquid (DCP-DMEM-GQB1X) - Quadruple-stage filtration system (0.1 micron x2 + 0.04 micron x2) 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-GQB1X
Applications

Optimized for next-generation cell biology platforms

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

Automated Bioreactors & Robotics

Next-Generation System Uptime

An optional 0.01 µm (10 nm) MPS Grade ultra nano-filtered variant of this formulation is available for automated bioreactor and liquid-handling robotics platforms where valve and sensor protection is critical.

  • Total particulate exclusion beyond the 0.04 µm Microfluidics Suitable tier
  • Valve and sensor protection for automated perfusion systems
  • Extended perfusion stability in closed-loop bioreactor systems

Inquiry Required: The 0.01 µm MPS Grade variant is available by request. Contact support@diagnocine.com.

Microfluidics

Micro Physiological System (MPS) & Chip

Ultra-low particulate media filtered to a 0.04 µm final cut-off for perfusion in organ chips, tissue chips (ToC), and body-on-a-chip (BoC) devices.[4]

OoCToCBoCMPS
Cancer Biology

Warburg Effect & Metabolic Research

Glucose-free formulation retaining sodium pyruvate as the sole carbon source, suited to Warburg-effect studies, aerobic glycolysis, and cancer metabolomics.[5]

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

iPSC-Derived Models

Ultra-clean, low-endotoxin baseline minimizes non-specific signals in iPSC differentiation and functional organoid readouts.

iPSC-NeuronsiPSC-CMiPSC-Hep
Vascular Biology

Endothelial & Primary Cells

Particle-reduced 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; this formulation contains phenol red.

13C tracingNMR
Live-Cell Imaging

Microscopy & Optical Sensing

Ultra-low particulate medium 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, Sodium Bicarbonate: 1X Liquid is released against comprehensive multi-parameter QC specifications.

Physical & Chemical Parameters
Parameter Specification
Formulation [+] Phenol Red, Calcium, Magnesium, Sodium Pyruvate · [-] Glucose, L-Glutamine, Sodium Bicarbonate
Appearance Clear solution
pH USP <791> 7.4
Osmolality USP <785> 310 - 350 mOsm/kg
Glucose Removed
L-Glutamine Removed ([-])
Sodium Pyruvate 110 mg/L ([+])
Phenol Red 15.9 mg/L ([+])
Sterility, Purity & Safety Parameters
Parameter Specification
Endotoxin USP <85> < 0.05 EU/mL (batch release specification)
Sterility USP <71> No growth after 14 days
Mycoplasma 0.1 µm and 0.04 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, away from bright light
Freeze–thaw Do not freeze
Shelf life 12 months from date of manufacture, unopened
Shipping Cold pack (2–8°C)
CO2 requirement Bicarbonate-free; suitable for CO2-independent culture. Add 10-25 mM HEPES for enhanced pH stability if 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 alignment 21 CFR Part 820 (QMSR) aligned
Production method Micro-batch; Totowa, NJ, USA
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: 30 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 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 42.000
L-Isoleucine 73-32-5 105.000
L-Leucine 61-90-5 105.000
L-Lysine hydrochloride 657-27-2 146.000
L-Methionine 63-68-3 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
Phenol red sodium salt 34487-61-1 15.900
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 is 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

18.2 MΩ·cm resistivity with tight trace-metal and organic-carbon (TOC) control. Formulated to support sensitive biosensor and TEER-based assay conditions.

biotech

ISO Class 5 Fill & Finish

Validated ISO Class 5 laminar-flow workstation with real-time particle monitoring, preserving filtration gains in the final container.

assignment

Micro-Batch Precision

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

Endotoxin — USP <85> BET

LAL assay; assay sensitivity 0.005 EU/mL. Batch release specification: < 0.05 EU/mL.

Particulate — USP <788> Method 1

Light Obscuration Particle Count Test performed per manufacturing batch; results reported on the Certificate of Analysis.

Osmolality — USP <785>

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

Certificate of Analysis (CoA)

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

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. Email support@diagnocine.com.
Product Comparison

How DCP-DMEM-GQB1X compares

Comparative filtration architecture, mycoplasma control, and QC depth relative to conventional 0.22 µm filtered DMEM for MPS and microfluidic applications.

Parameter DCP-DMEM-GQB1X (FluxMPS™) Standard DMEM (0.22 µm) Competitor DMEM (0.22 µm)
Grade Microfluidics Suitable Standard grade Standard grade
Formulation definition [+] Phenol Red, Calcium, Magnesium, Sodium Pyruvate · [-] Glucose, L-Glutamine, Sodium Bicarbonate Standard Standard
Final filtration pore size 0.04 µm (40 nm) 0.22 µm 0.22 µm
Filtration stages 4 (0.1 µm ×2 + 0.04 µm ×2) 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)
Sterility testing (USP <71>) check_circle 14-day test per batch Not specified Not specified
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, Sodium Bicarbonate: 1X Liquid (DCP-DMEM-GQB1X).

DCP-DMEM-GQB1X is engineered for organ-on-a-chip, microfluidic, and microphysiological system (MPS) applications. The 0.04 µm final filtration stage, applied twice within the quadruple-stage train (0.1 µm ×2 + 0.04 µm ×2), reduces sub-micron particulates and mycoplasma-size contaminants that can obstruct microchannel flow in standard 0.22 µm-filtered media.
Four sequential filtration passes (0.1 µm, 0.04 µm, 0.1 µm, 0.04 µm) are applied as two dedicated prefilter/final-filter pairs, retaining mycoplasma-size organisms (0.2–0.3 µm) and sub-visible particulates that a single 0.22 µm pass does not remove. Particulate testing follows USP <788> Method 1 (Light Obscuration).
DCP-DMEM-GQB1X is formulated without glucose to enable precise control of the carbon source for Warburg-effect studies, glycolysis inhibition, and 13C metabolic tracing. This formulation already contains 110 mg/L sodium pyruvate as an alternative carbon source. Add D-glucose at your desired concentration (typically 1–4.5 g/L) if glycolytic flux is required for your assay. Contact support@diagnocine.com for pre-supplemented variants.
No sodium bicarbonate is present in this formulation, so DCP-DMEM-GQB1X is suitable for CO2-independent incubation. Add 10–25 mM HEPES for enhanced pH stability outside a CO2 incubator. Contact support@diagnocine.com for a HEPES-supplemented variant.
Yes. DCP-DMEM-GQB1X is a basal medium compatible with FBS (2–10%), human serum, GlutaMAX, EGF, FGF, VEGF, and antibiotics. Pre-filter serum and other protein-containing additions through a 0.2 µm low-protein-binding PES or PVDF filter before combining; defined, protein-free additions may be filtered at 0.1 µm. Do not use a 0.04 µm filter for supplement filtration, as it will retain serum proteins and lipoproteins.
Endotoxin is controlled per manufacturing batch to a release specification of less than 0.05 EU/mL, tested by LAL assay per USP <85> (Bacterial Endotoxins Test; assay sensitivity 0.005 EU/mL). Every batch is tested before release. Lot-specific results are available on the Certificate of Analysis at support@diagnocine.com.
Yes — a full CoA per lot includes lot number, expiry, appearance, pH (USP <791>), osmolality (USP <785>), endotoxin (USP <85>), sterility (USP <71>), and mycoplasma filtration status. 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

Satisfaction
Quality Rating
Value Rating
Style Rating
X