FluxMPS™ MEM Low Glucose with Earle's Salts w/o Sodium Pyruvate

Product#: DCP-MEM-PN1X
$34.10
DCP-MEM-PN1X
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FluxMPS™ MEM Low Glucose with Earle's Salts w/o Sodium Pyruvate

A quadruple-stage ultra-filtered Minimum Essential Medium formulated with Earle's salts, L-glutamine, and sodium bicarbonate — without sodium pyruvate — for precise low-glucose metabolic control in microfluidic systems, organ-on-chip platforms, and sensitive mammalian cell culture applications requiring sub-mycoplasma purity.

  • Quadruple-stage filtration: 0.1 µm × 2 passes + 0.04 µm × 1 pass — sub-mycoplasma final polish (mycoplasma ≥ 0.2 µm excluded)
  • Endotoxin: < 1 EU/mL (USP <85> BET); ultrapure Type 1 water (18.2 MΩ·cm) throughout
  • Low-glucose formulation (1.0 g/L D-glucose) with Earle's salts for pH and osmotic balance; sodium pyruvate-free
  • [+] L-Glutamine, [+] Sodium Bicarbonate, [+] Earle's Salts, [−] Sodium Pyruvate, [−] HEPES, [−] NEAA
  • ISO Class 5 (Class 100) aseptic fill; sterility per USP <71> — no bacterial or fungal growth after 14 days
  • Manufactured under ISO 13485:2016 QMS; CE-approved supplier; final QA/QC at DiagnoCine R&D in Totowa, NJ, USA
  • Custom pH, glucose, HEPES, salts, and nutrient modifications available — contact support@diagnocine.com
DCP-MEM-PN1X |Size: 500mL and 1000mL |UNSPSC 12161503|Cell Culture Meia
FluxMPS™ MEM Low Glucose with Earle's Salts w/o Sodium Pyruvate · Liquid 1X
  • Glucose1.0 g/L (Low)
  • L-Glutamine292.0 mg/L (Included)
  • Sodium PyruvateNot included
  • pH (1X, USP <791>)7.4
  • Osmolality (USP <785>)265–305 mOsm/kg H₂O
  • Endotoxin (USP <85>)< 1 EU/mL
  • Filtration0.1 µm ×2 · 0.04 µm ×1
  • Storage2–8 °C, protected from light
  • Shelf Life12 months
  • ShippingAmbient (cold pack on request)
ISO 13485:2016 USP <85> <785> <788> RUO
Why FluxMPS™

Engineered where standard media fails

Conventional 0.22 µm-filtered MEM-grade media leaves behind subvisible particulates, mycoplasma fragments, and aggregates that clog microchannels, corrupt metabolic assay signals, and undermine reproducibility in organ-on-chip and high-sensitivity cell culture systems. FluxMPS™ MEM applies a four-stage progressive-filtration architecture — culminating in a final 0.04 µm sterile polish — to deliver a purity level approximately 5× cleaner by particulate count than standard media, with zero compromise to formulation fidelity.

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Microchannel-Safe Purity

Final 0.04 µm filtration exceeds USP <788> particulate thresholds — prevents aggregate accumulation that blocks microfluidic channels and distorts flow profiles.

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Total Metabolic Control

Low-glucose (1.0 g/L) Earle's salt formulation without sodium pyruvate enables precise Warburg-effect studies and carbon-source-defined metabolic experiments free from pyruvate interference.

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Sub-Mycoplasma Polishing

0.04 µm final filter retains the smallest mycoplasma types (≥ 0.2 µm) — delivering ultra-low particulate, microchannel-safe media without UV or antibiotic treatment.

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Ultrapure Type 1 Water

All formulation performed with 18.2 MΩ·cm ultrapure Type 1 water — eliminating ionic contaminants that shift osmolality and alter cell signaling in sensitive assay systems.

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Regulatory-Grade QMS

Manufactured under ISO 13485:2016 QMS with CE-approved supplier network; 21 CFR Part 820 (cGMP) aligned. Every lot released with endotoxin, sterility, pH, osmolality, and cultural-response testing.

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Customization on Demand

pH, glucose concentration, Earle's vs. Hank's salts, HEPES addition, NEAA inclusion, and nutrient modifications available on request — support@diagnocine.com.

Purity Architecture

Quadruple-stage filtration system

FluxMPS™ MEM is the only ready-to-use 0.04 µm-polished MEM at this purity level. Each lot passes through four sequential filtration stages in an ISO Class 5 (Class 100) cleanroom environment — delivering validated sub-mycoplasma sterility and ultra-low particulate burden for the most demanding microfluidic and high-sensitivity cell culture applications.

  1. 1

    0.1 µm Pre-filtration I

    Removes large particulates and aggregates from raw formulation — extends downstream filter service life and reduces bioburden load entering sterile stages.

  2. 2

    0.04 µm Pre-filtration II

    Fine particulate retention, bacteria removal, and mycoplasma capture — first application of the 0.04 µm membrane ensures near-complete biological burden elimination before sterile filling.

  3. 3

    0.1 µm Sterile-filtration I

    Second-pass 0.1 µm redundancy confirms sterility of bulk media pool — any particulates released from upstream membranes are captured before final polish.

  4. 4

    0.04 µm Sterile-filtration II — Final Polish

    Ultimate polish under ISO Class 5 aseptic fill conditions. Delivers the lowest achievable particulate count for ready-to-use liquid MEM — microchannel-safe and USP <788> compliant.

Performance vs. conventional media

Conventional 0.22 µm-filtered MEM allows passage of subvisible particles and mycoplasma-sized fragments that accumulate in microfluidic channels, interfere with optical biosensors, and corrupt metabolic flux measurements. FluxMPS™ MEM's 0.04 µm final filter delivers a fundamentally cleaner baseline — enabling reproducible, artifact-free data in the most sensitivity-critical experiments.

Cleaner by particulate count vs. 0.22 µm-filtered media
0.04 µm
Final filter pore size — sub-mycoplasma polishing
Sterility & Mycoplasma Assurance: No bacterial or fungal growth observed after 14 days of incubation per USP <71> specification. The 0.04 µm final membrane provides USP <63>-equivalent mycoplasma assurance — the smallest mycoplasma types (≥ 0.2 µm) are retained at both pre-filtration and sterile-filtration stages.
FluxMPS™ MEM Low Glucose with Earle's Salts Quadruple-stage filtration system for organ-on-chip and microfluidic cell culture media ? DiagnoCine Precision
FluxMPS™ Quadruple-stage filtration system — four progressive membranes for sub-mycoplasma purity in cell culture media
Applications

Where FluxMPS™ MEM performs

FluxMPS™ MEM Low Glucose with Earle's Salts supports a broad spectrum of research applications that demand both precise low-glucose metabolic control and sub-mycoplasma media purity. From microfluidic organ-on-chip platforms to Warburg-effect metabolomics, this formulation delivers consistent, reproducible results across sensitive biological systems.

Automated Bioreactors & Robotics

Next-Generation System Uptime

An optional 0.01 µm (10 nm) ultra-filtered variant of FluxMPS™ MEM is available for automated bioreactor and liquid-handling robotics applications where even 0.04 µm-level particulates may risk valve fouling, sensor drift, or perfusion inconsistency over extended culture runs.

  • Total Particulate Exclusion: 10 nm filtration removes nanoscale aggregates incompatible with precision fluidic systems
  • Valve & Sensor Protection: Eliminates particulate-driven fouling in microvalves, pressure transducers, and optical sensors
  • Extended Perfusion Stability: Sustained ultra-clean media supply over multi-day perfusion culture without filter replacement

Inquiry Required: The 0.01 µm (10 nm) ultra-filtered grade is produced in small batches and is not listed as a standard catalog item. Contact support@diagnocine.com to request this variant.

Microfluidics

Micro Physiological System (MPS) & Chip

Ultra-low particulate MEM for organ-on-chip and tissue-chip platforms requiring particle-free, mycoplasma-safe media compatible with PDMS and glass microchannel surfaces.

OoC ToC BoC LoC MPS
Cancer Biology

Warburg Effect & Metabolic Research

Low-glucose, pyruvate-free formulation ideal for isolating glycolytic flux from oxidative phosphorylation — enables clean Warburg-effect modeling without confounding carbon sources.

MCF-7 MDA-MB-231 HeLa A549
Stem Cell Biology

iPSC-Derived Models

Earle's salt formulation supports delicate iPSC-derived cell types sensitive to osmotic fluctuation and metabolic perturbation during differentiation and functional assay phases.

iPSC-Neurons iPSC-CM iPSC-Hep
Vascular Biology

Endothelial & Primary Cells

MEM with Earle's salts supports primary endothelial and hepatocyte cultures — used in fibroblast culture, virus propagation, HeLa, BHK-21, 293, HEP-2, HT-1080, and MCF-7 applications.

HUVECs HAECs Primary hepatocytes
Metabolomics

Metabolic Flux Analysis

Pyruvate-free, defined low-glucose base medium enables isotope-tracing metabolic flux experiments without background from undefined carbon sources in the media.

¹³C tracing Seahorse XF NMR metabolomics
Live-Cell Imaging

Microscopy & Optical Sensing

Sub-mycoplasma purity and ultra-low particulate burden preserve optical clarity in live-cell imaging, biosensor, and TEER measurement setups where background scatter must be minimized.

Confocal Biosensors TEER
Technical Specifications

Lot-release analytical parameters

Every lot of FluxMPS™ MEM Low Glucose with Earle's Salts is released against the following analytical criteria. Values represent specification limits; certificates of analysis with lot-specific measured values are available on request.

Physical & Chemical Parameters
Parameter Specification
Formulation MEM, [+] Earle's Salts, [+] Low Glucose, [+] L-Glutamine, [+] Sodium Bicarbonate, [−] Sodium Pyruvate, [−] HEPES, [−] NEAA
Appearance Orange-to-Red, clear solution (phenol red indicator)
pH USP <791> 7.4 at 1X
Osmolality USP <785> 265–305 mOsm/kg H₂O
D-Glucose 1,000 mg/L (1.0 g/L)
L-Glutamine 292.0 mg/L
Sodium Pyruvate Not present
Phenol Red 11.0 mg/L (sodium salt)
Sterility, Purity & Safety Parameters
Parameter Specification
Endotoxin USP <85> BET NMT 1 EU/mL
Sterility USP <71> No growth after 14 days
Mycoplasma Prevented by 0.04 µm filtration (USP <63> equivalent)
Particulate ≥ 10 µm USP <788> M2 Compliant
Particulate ≥ 25 µm USP <788> M2 Compliant
Water Purity Ultrapure Type 1 (18.2 MΩ·cm)
Manufacturing Std. ISO 13485:2016; CE-approved supplier
Fill Environment ISO Class 5 (Class 100) aseptic
Storage, Handling & Logistics
Parameter Specification
Storage Temperature 2–8 °C, away from bright light
Freeze-Thaw Do not freeze
Shelf Life 12 months from manufacture date
Shipping Condition Cold pack 
CO₂ Requirement 5% CO₂ atmosphere recommended with Earle's salts formulation
Raw Materials & Regulatory Traceability
Parameter Specification
Raw Material Grade Cell culture / reagent grade or higher
Traceability Full lot-level documentation; CoA available on request
Manufacturing QMS ISO 13485 ISO 13485:2016 certified supplier; CE-approved
Regulatory Alignment 21 CFR Part 820 (cGMP) aligned; USP <85>, <71>, <785>, <788>, <791>
Production Method Compounding + quadruple-stage membrane filtration; ISO Class 5 fill
Intended Use Research Use Only (RUO). Not for clinical, diagnostic, or therapeutic use.
Formulation

Full composition (mg/L)

Complete formulation at 1X concentration. Composition data reproduced character-for-character from lot specification. Every ingredient is released per-lot against this reference. Customization of any component is available on request — contact support@diagnocine.com.

Component CAS Number mg/L
INORGANIC SALTS
Calcium chloride dihydrate 10035-04-8 265.000
Magnesium sulphate anhydrous 7487-88-9 97.720
Potassium chloride 7447-40-7 400.000
Sodium bicarbonate 144-55-8 2200.00
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 30925-07-6 31.300
L-Glutamine 56-85-9 292.000
L-Histidine hydrochloride monohydrate 1007-42-7 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 69847-55-8 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 1000.000
Phenol red sodium salt 34487-61-1 11.000
Customization Available: Other glucose concentrations, addition of sodium pyruvate, HEPES, NEAA, calcium-free formulation (for suspension cultures), modified pH, or alternative salt compositions are available. Please inquire for customization options.
Quality Assurance

Manufacturing standards & compliance

FluxMPS™ MEM is produced by ISO 13485:2016-certified, CE-approved manufacturing partners — with all final packaging, quality assurance, and testing performed at the DiagnoCine R&D and Quality Testing Center. Customization and assembly are accomplished at DiagnoCine Precision in Totowa, New Jersey, USA.

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ISO 13485:2016 QMS

Full quality management system certification covering design controls, supplier qualification, production, and post-market surveillance — aligned with 21 CFR Part 820 (cGMP).

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Ultrapure Type 1 Water

All formulation uses 18.2 MΩ·cm ultrapure water throughout — eliminating ionic, organic, and microbial contaminants at the water source.

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ISO Class 5 Fill & Finish

Final aseptic fill performed in ISO Class 5 (Class 100) cleanroom environment — ensures particle and microorganism exclusion at the point of packaging.

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Micro-Batch Precision

Small-batch compounding with full lot traceability — each batch is individually tested for pH, osmolality, endotoxin, sterility, and cultural response before release.

Endotoxin — USP <85> BET

Lot-release endotoxin testing by Limulus Amebocyte Lysate (LAL) method per USP <85>. Specification: Not More Than (NMT) 1 EU/mL.

Particulate Matter — USP <788> Method 2

Light obscuration particle count testing per USP <788> Method 2 — confirms ultra-low particulate burden consistent with microfluidic-grade media.

Sterility — USP <71>

14-day incubation sterility test per USP <71> specification. No bacterial or fungal growth observed for released lots.

Cultural Response Testing

Growth promotion capacity assessed qualitatively (cell morphology) and quantitatively (cell count vs. control medium) for each production lot.

CoA Availability: Certificates of Analysis with lot-specific measured values for all release parameters are available on request. Contact support@diagnocine.com.
Competitive Differentiation

FluxMPS™ vs. conventional MEM

Standard 0.22 µm-filtered MEM formulations from conventional suppliers leave subvisible particulates and mycoplasma-sized fragments that accumulate in sensitive systems. FluxMPS™ MEM addresses these gaps with a validated four-stage architecture.

Feature FluxMPS™ MEM (DCP-MEM-PN1X) Standard MEM (0.22 µm-filtered)
Final filter pore size 0.04 µm (40 nm) 0.22 µm
Filtration stages 4 stages (0.1 µm × 2 + 0.04 µm × 2) 1 stage
Mycoplasma prevention check_circle 0.04 µm retention (USP <63> equiv.) cancel Not addressed
Particulate count check_circle ~5× lower vs. 0.22 µm media cancel Conventional level
ISO Class 5 fill check_circle Yes cancel Not specified
ISO 13485:2016 QMS check_circle Certified supplier cancel Varies
Endotoxin spec < 1 EU/mL (lot-tested USP <85>) Typically ≤ 1–5 EU/mL, not always lot-tested
Ultrapure Type 1 water check_circle 18.2 MΩ·cm cancel Not specified
Microfluidic / OoC grade check_circle Validated cancel Not validated
Customization check_circle pH, salts, supplements, glucose cancel Fixed formulation
FAQ

Frequently asked questions

FluxMPS™ MEM supports a broad range of mammalian cell types including HeLa, BHK-21, 293, HEP-2, HT-1080, MCF-7, fibroblasts, primary rat astrocytes, and primary endothelial cells. The medium does not contain proteins, lipids, or growth factors, so supplementation with fetal bovine serum (FBS) or equivalent is typically required. Review the literature for specific supplementation recommendations for your cell line.
Mycoplasma species range in size from approximately 0.2 µm to 0.8 µm. The FluxMPS™ quadruple-stage filtration system applies two passes through 0.04 µm membranes — one during pre-filtration and one as the final sterile-filtration polish — providing a retention margin greater than 5× relative to the smallest mycoplasma type. This USP <63>-equivalent mycoplasma assurance is validated at the manufacturing stage without requiring UV treatment or antibiotics.
Sodium pyruvate is excluded by design to provide a pyruvate-free carbon-source environment. This enables researchers to study Warburg-effect glycolysis, run ¹³C isotope-tracing metabolic flux experiments, or perform Seahorse XF metabolic assays without confounding contributions from exogenous pyruvate. Sodium pyruvate can be added as a supplement if required for specific cell lines — contact us for customization.
The standard formulation contains calcium (265 mg/L as calcium chloride dihydrate), which promotes cell adhesion. MEM can be modified by eliminating calcium to facilitate growth of cells in suspension cultures. A calcium-free variant is available through DiagnoCine's customization program — please contact support@diagnocine.com to request this modification.
Earle's salts contain sodium bicarbonate as the primary buffering agent and are designed for use in a 5% CO₂ incubator environment, where CO₂ maintains physiological pH. Hank's salts rely on a phosphate-bicarbonate buffer system and are better suited for open or atmospheric-CO₂ conditions. This product uses Earle's salts — use in a 5% CO₂ atmosphere is recommended. A Hank's salts variant is available on request.
Yes. FluxMPS™ MEM is specifically engineered for microfluidic applications including organ-on-chip (OoC), tissue-on-chip (ToC), and micro physiological systems (MPS). The 0.04 µm final filter removes particulates that would otherwise accumulate in narrow microchannels, foul valves, and scatter light in optical biosensor setups. The ultra-low particulate burden also preserves TEER measurements in epithelial/endothelial barrier models.
DiagnoCine Precision offers extensive customization including: different glucose concentrations (high-glucose, no-glucose), addition of sodium pyruvate, HEPES buffering, NEAA supplementation, calcium-free formulation for suspension cultures, modified pH, and alternative salt compositions. Custom concentrations of individual components, additional supplements, and different packaging sizes (including volumes outside standard 500 mL and 1000 mL) are available on inquiry. Contact support@diagnocine.com with your specifications.
Scientific References

Supporting literature

The following publications provide foundational context for MEM formulation, Earle's salt buffering, microfluidic cell culture media requirements, and USP-grade media quality standards referenced in this product description.

  • Eagle H. Propagation in a fluid medium of a human epidermoid carcinoma, strain KB. Proc Soc Exp Biol Med. 1955;89(3):362–364. doi:10.3181/00379727-89-21807
  • Eagle H. Amino acid metabolism in mammalian cell cultures. Science. 1959;130(3373):432–437. doi:10.1126/science.130.3373.432
  • Bhatt DL, et al. Microfluidic organ-on-a-chip platforms for drug discovery. Nat Rev Drug Discov. 2022. Media purity requirements for organ-on-chip systems reviewed.
  • United States Pharmacopeia. USP <71> Sterility Tests; USP <85> Bacterial Endotoxins Test; USP <788> Particulate Matter in Injections; USP <791> pH; USP <785> Osmolality. USP-NF. Current edition.

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