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

Product#: DCP-DMEML-QPBR1X
$44.00
DCP-DMEML-QPBR1X
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verified ISO 13485 Certified Manufacturing

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

FluxMPS™ DCP-DMEML-QPBR1X is an MPS-grade, ultra-filtered DMEM Low Glucose formulation engineered for microphysiological systems, organ-on-a-chip (OoC), and microfluidic tissue models. Processed through a Quadruple-stage filtration system (0.1 µm ×2 + 0.04 µm ×2), it delivers approximately 5× lower particulate counts than conventional 0.22 µm–filtered media. Formulation: [+] Low Glucose | [-] L-Glutamine, [-] Sodium Pyruvate, [-] Sodium Bicarbonate, [-] Phenol Red.

  • 0.04 µm final nano-filtration — sub-mycoplasma purity for microfluidic channels below 100 µm
  • Quadruple-stage sequential filtration: 0.1 µm pre-I → 0.04 µm pre-II → 0.1 µm sterile-I → 0.04 µm final polish
  • Endotoxin < 0.05 EU/mL (LAL, USP <85>)
  • Formulation: [+] Low Glucose | [-] L-Glutamine, [-] Sodium Pyruvate, [-] Sodium Bicarbonate, [-] Phenol Red
  • Ultrapure Type 1 water (18.2 MΩ·cm), ISO 13485:2016 QMS, ISO Class 5 fill
  • Custom pH, salts, and nutrient adjustments available on request
SKU: DCP-DMEML-QPBR1X | Size: 500 mL and 1000 mL| UNSPSC 41122100 Cell Culture Media
Dulbecco’s Modified Eagle Medium (DMEM), Low Glucose w/o L-Glutamine, Sodium Pyruvate, Sodium Bicarbonate, Phenol Red: 1X Liquid 
  • Formulation[+] Low Glucose | [-] L-Glutamine, [-] Sodium Pyruvate, [-] Sodium Bicarbonate, [-] Phenol Red
  • AppearancePale yellow colored, clear solution
  • pH (USP <791>)7.4
  • Osmolality (USP <785>)310.00–350.00 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
  • Total ingredients29
  • Storage2–8°C, away from light
  • Shelf Life12 months
ISO 13485:2016 USP <85> <785> <788> RUO
Why FluxMPS™

Engineered where standard media fails

Conventional 0.22 µm–filtered media passes mycoplasma, subvisible particulates, and endotoxin fragments that clog microfluidic channels and corrupt sensor signals. FluxMPS™ eliminates these failure modes with four-stage sub-0.04 µm filtration.

filter_alt

Microchannel-safe purity

0.04 µm final filtration; USP <788> particulate compliance ensures safe perfusion in every chip geometry.

target

Total metabolic control

Selective inclusion/exclusion of glutamine, pyruvate, bicarbonate, and HEPES for precise nutrient and buffer definition.

water_drop

Ultrapure-grade water

Ultrapure Type 1 water (18.2 MΩ·cm), USP <85> — eliminates ionic contaminants interfering with TEER and electrophysiology.

visibility

Low background for imaging

Ultra-low particulate count; phenol red–free variants eliminate autofluorescence for confocal and biosensor applications.

science

Rich, stable nutrient profile

29 ingredients verified per lot; micro-batch production with full traceability.

tune

Customization on demand

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

Purity Architecture

Quadruple-stage filtration system

Four serial filtration stages reaching a final 0.04 µm polish under ISO Class 5 aseptic conditions — delivering sub-mycoplasma purity unavailable from any conventional 0.22 µm filtered media.

  1. 1

    0.1 µm Pre-filtration I — Large Particulate Removal

    Removes large aggregates and particulates; protects downstream 0.04 µm membranes and chip geometries.

  2. 2

    0.04 µm Pre-filtration II — Mycoplasma Barrier

    Retains mycoplasma (0.1–0.3 µm) and fine particulates — absent from standard 0.22 µm filtration.

  3. 3

    0.1 µm Sterile-filtration I — Second-pass Redundancy

    Second-pass sterility redundancy; no breakthrough from Stage 1.

  4. 4

    0.04 µm Sterile-filtration II — Final Polish

    Ultimate sub-mycoplasma polish; ISO Class 5 aseptic fill & finish.

Performance vs. conventional media

FluxMPS™ DCP-DMEML-QPBR1X delivers approximately 5× lower particulate counts than standard 0.22 µm filtered media, with a confirmed mycoplasma barrier at every production stage.

Cleaner than 0.22 µm media by particulate count
0.04
µm Final pore size — sub-mycoplasma polishing
Sterility & Mycoplasma: No growth after 14-day incubation (USP <71>); mycoplasma-negative by 0.04 µm barrier — USP <63>–equivalent assurance every lot.
FluxMPS™ DCP-DMEML-QPBR1X Dulbecco’s Modified Eagle Medium (DMEM), Low Glucose w/o L-Glutamine, Sodium Pyruvate, Sodium Bicarbonate, Phenol Red: 1X Liquid ? Quadruple-stage filtration system: 0.1 μm Pre-filtration I, 0.04 μm Pre-filtration II mycoplasma barrier, 0.1 μm Sterile-filtration I, 0.04 μm Final Polish ? MPS-grade microfluidic cell culture media | Diagnocine
Figure 1. FluxMPS™ Quadruple-stage filtration system (0.1 µm ×2 + 0.04 µm ×2) for sub-mycoplasma purity in organ-on-a-chip applications.
© Diagnocine® — DCP-DMEML-QPBR1X
Applications

Designed for next-generation cell models

FluxMPS™ DCP-DMEML-QPBR1X supports demanding platforms from single-channel microfluidic chips to multi-organ body-on-a-chip systems.

Automated Bioreactors & Robotics

Next-Generation System Uptime

Optional 0.01 µm (10 nm) ultra-filtered variant available on request for automated bioreactor perfusion and robotic liquid handlers.

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

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

Microfluidics

Micro Physiological System (MPS) & Chip

Ultra-clean 0.04 µm–filtered media prevents microchannel clogging in complex multi-organ chip architectures.

OoCToCBoCLoCMPS
Bioproduction

CHO & Mammalian Cell Culture

Optimized for CHO, cancer cells, primary cells, and clonal growth in serum-free or low-serum conditions.

CHOMCF-7HeLaHEK293
Stem Cell Biology

iPSC-Derived Models

Ultra-low endotoxin (< 0.05 EU/mL) and mycoplasma-free certification for sensitive iPSC protocols.

iPSC-NeuronsiPSC-CMiPSC-Hep
Vascular Biology

Endothelial & Primary Cells

Particle-free, endotoxin-controlled media for HUVEC monolayer integrity and TEER monitoring.

HUVECsHAECsPrimary hepatocytes
Metabolomics

Metabolic Flux Analysis

Defined formulation provides a clean background for ¹³C isotope tracing and Seahorse XF assays.

¹³C tracingSeahorse XFNMR metabolomics
Live-Cell Imaging

Microscopy & Optical Sensing

Ultra-low particulate and (phenol red–free variants) zero autofluorescence for confocal and biosensor platforms.

ConfocalBiosensorsTEER
Technical Specifications

Analytical release specifications

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

Physical & Chemical Parameters
Parameter Specification
Formulation [+] Low Glucose | [-] L-Glutamine, [-] Sodium Pyruvate, [-] Sodium Bicarbonate, [-] Phenol Red
Appearance Pale yellow colored, clear solution
pH USP <791> 7.4 ± 0.2
Osmolality USP <785> 310.00–350.00 mOsm/kg H₂O
Total ingredients 29
Sterility, Purity & Safety
Parameter Specification
Endotoxin USP <85> BET < 0.05 EU/mL
Sterility USP <71> No growth / 14 days
Mycoplasma Negative (0.04 µm barrier)
Particulate ≥10 µm USP <788> NMT 25/mL
Particulate ≥25 µm USP <788> 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, away from light
Freeze-thaw Do not freeze
Shelf life 12 months from manufacture
Shipping condition Cold pack
CO₂ requirement CO₂-independent; use HEPES or organic buffer for pH control
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
Regulatory alignment 21 CFR Part 820 (cGMP) aligned
Production method Micro-batch, per-lot QC release
Intended use Research Use Only (RUO)
Formulation

Full composition (mg/L)

29 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 sulphate 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
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 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 69847-15-0 103.790
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 1000.000
Custom formulation: Contact support@diagnocine.com for DCP-DMEML-QPBR1X custom specifications.
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 and CE-approved facilities. Final QA at DiagnoCine R&D Center, Totowa, NJ, USA.

water_drop

Ultrapure Type 1 Water

18.2 MΩ·cm, USP <85> resistivity — eliminates ionic contaminants affecting cell signaling and sensor measurements.

biotech

ISO Class 5 Fill & Finish

Aseptic fill in validated ISO Class 5 (Class 100) laminar-flow workstations.

assignment

Micro-Batch Precision

Small-batch production, full per-lot traceability, Certificate of Analysis for every lot.

Endotoxin — USP <85> BET

LAL assay, release limit: < 0.05 EU/mL per lot.

Particulate — USP <788> Method 2

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

Osmolality — USP <785>

Freezing-point osmometry. Target: 310.00–350.00 mOsm/kg H₂O.

Documentation & CoA

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

Certificate of Analysis: Request for any DCP-DMEML-QPBR1X lot at support@diagnocine.com.
Product Comparison

How DCP-DMEML-QPBR1X compares

FluxMPS™ DCP-DMEML-QPBR1X vs. conventional 0.22 µm–filtered DMEM Low Glucose formulations.

Parameter DCP-DMEML-QPBR1X (FluxMPS™) Conventional DMEM Low Glucose
(0.22 µm filtered)
Standard Alt.
(0.22 µm filtered)
Maximum-minimal base — only Low Glucose included, all components researcher-defined 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 barrier check_circle Yes cancel No cancel No
Endotoxin specification < 0.05 EU/mL NMT 1 EU/mL NMT 1 EU/mL
USP <788> 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 compatible check_circle MPS-grade cancel Risk of clogging cancel Risk of clogging
Custom formulation check_circle Available cancel Fixed cancel Fixed
FAQ

Frequently asked questions

Common questions about FluxMPS™ DCP-DMEML-QPBR1X.

Yes. DCP-DMEML-QPBR1X is processed through a Quadruple-stage filtration system reaching 0.04 µm final pore size, delivering ultra-low particulate levels for MPS, OoC, tissue-on-a-chip (ToC), and lab-on-a-chip (LoC) platforms.
FluxMPS™ uses four sequential filters — 0.1 µm pre-filtration I, 0.04 µm pre-filtration II (mycoplasma barrier), 0.1 µm sterile-filtration I, and 0.04 µm final polish — resulting in approximately 5× fewer particles and confirmed mycoplasma retention at every production stage.
This is the most minimal DMEM base — containing only the core salt and amino acid scaffold with low glucose. Every nitrogen source, carbon source, pH buffer, and optical indicator is left to the researcher for fully defined, precisely controlled culture environments.
CO₂-independent; use HEPES or organic buffer for pH control
Yes. Add FBS (typically 5–10%), serum-free supplements, growth factors, antibiotics, or custom nutrients as required. Contact support@diagnocine.com for custom co-formulation.
Each lot is tested by LAL assay (USP <85>). FluxMPS™ DCP-DMEML-QPBR1X is produced to meet < 0.05 EU/mL — 20× below the 1 EU/mL common for cell culture grade reagents.
Yes. A full CoA per lot covers: appearance, pH (USP <791>), osmolality (USP <785>), sterility (USP <71>), endotoxin (USP <85>), mycoplasma, particulate count (USP <788> Method 2), and raw-material traceability. Request at support@diagnocine.com.
Scientific References

Supporting literature

Key peer-reviewed publications supporting MPS-grade, ultra-filtered media in organ-on-a-chip and microfluidic 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. Ham RG. Clonal growth of mammalian cells in a chemically defined, synthetic medium. Proc Natl Acad Sci USA. 1965;53:288–293. doi:10.1073/pnas.53.2.288
  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. 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
  6. Schimek K, et al. Integrating biological vasculature into a multi-organ-chip microsystem. Lab Chip. 2013;13:3588–3598. doi:10.1039/c3lc50217a
  7. Luni C, et al. High-efficiency cellular reprogramming with microfluidics. Nat Methods. 2016;13:446–452. doi:10.1038/nmeth.3832
  8. 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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