FluxMPS™ CMRL 1066 Medium w/o Sodium Bicarbonate, Phenol Red: 1X Liquid

Product#: DCP-CMRL-BR1X
$64.90
DCP-CMRL-BR1X
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ISO 13485 Certified Manufacturing

FluxMPS™ CMRL 1066 Medium w/o Sodium Bicarbonate, Phenol Red: 1X Liquid

FluxMPS™ CMRL 1066 Medium w/o Sodium Bicarbonate, Phenol Red: 1X Liquid is an MPS-grade, ultra-filtered cell culture medium engineered for organ-on-a-chip (OoC), tissue-on-a-chip (ToC), and microphysiological system (MPS) applications. Processed through a proprietary Quadruple-stage filtration system (0.1 µm ×2 + 0.04 µm ×2), it delivers approximately 5× cleaner media than conventional 0.22 µm-filtered formulations by particulate count — making it microchannel-safe from day one.

  • Quadruple-stage nano-filtration: 0.1 µm (Pre-filtration I & III) + 0.04 µm (Pre-filtration II & Final Polish)
  • Endotoxin: less than 0.05 EU/mL (USP <85> BET verified)
  • CMRL 1066 Medium w/o Sodium Bicarbonate, Phenol Red: 1X Liquid base formulation; pH 7.4 (USP <791>)
  • Prepared with Ultrapure Type 1 water (18.2 MΩ·cm), USP <85>
  • ISO Class 5 aseptic fill & finish; ISO 13485:2016 QMS manufacturing
  • Mycoplasma-controlled via sub-0.1 µm final filter stage
  • Custom formulations available — pH, glucose, salts, HEPES, and nutrient composition on request
DCP-CMRL-BR1X | UNSPSC 41122100 Cell Culture MediaSize: 500 mL and 1000 mL
CMRL 1066 Medium w/o Sodium Bicarbonate, Phenol Red: 1X Liquid — Liquid, 1X
  • Glucose1000 mg/L (1.0 g/L)
  • L-Glutamine100 mg/L
  • Sodium PyruvateNot present
  • HEPESNot present
  • pH (USP <791>)7.4
  • Osmolality (USP <785>)Contact for specification
  • Endotoxin (USP <85>)less than 0.05 EU/mL
  • Filtration0.1 µm ×2 + 0.04 µm ×2
  • Storage2–8°C, protect 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 carry mycoplasma-sized particulates (0.1–0.3 µm), subvisible debris, and endotoxin spikes that accumulate inside microchannels — corrupting biosensor readings, triggering inflammation in primary cultures, and shortening device lifetimes. FluxMPS™ eliminates these failure modes at the source.

filter_alt

Microchannel-safe purity

0.04 µm final filter stage retains particles down to sub-mycoplasma size; USP <788> particulate compliance verified per lot.

target

Total metabolic control

User-defined carbon source, Warburg-ready glucose-free options, and precise nutrient concentrations for metabolic flux experiments.

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Ultrapure-grade water

Prepared with Type 1 water (18.2 MΩ·cm), meeting USP <85> conductivity standards and minimizing ionic background noise.

visibility

Low background for imaging

Ultra-clean formulation delivers minimal autofluorescence — ideal for confocal microscopy, live-cell biosensors, and TEER measurements.

science

Rich, stable nutrient profile

Micro-batch precision manufacturing locks in amino acid and vitamin concentrations, ensuring lot-to-lot reproducibility critical for long-term perfusion studies.

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Customization on demand

pH, glucose concentration, salts, HEPES, and full nutrient composition available on request. Contact support@diagnocine.com.

Purity Architecture

Quadruple-stage filtration system

FluxMPS™ CMRL 1066 Medium w/o Sodium Bicarbonate, Phenol Red: 1X Liquid is the only ready-to-use formulation processed through a four-stage serial filtration sequence that reaches 0.04 µm — eliminating mycoplasma, subvisible particles, and bioburden that 0.22 µm filtration cannot address.

  1. 1

    0.1 µm Pre-filtration I

    Removes large particulates and aggregates; protects downstream filter geometry and extends filter life across microchannel-scale flow paths.

  2. 2

    0.04 µm Pre-filtration II

    Fine particulate and bacteria removal; retains mycoplasma (typical diameter 0.1–0.3 µm) — a critical step absent in standard 0.22 µm filtration.

  3. 3

    0.1 µm Sterile-filtration I

    Second-pass redundancy for residual contaminants and bioburden; ensures no breakthrough from Stage 1 reaches the final filter.

  4. 4

    0.04 µm Sterile-filtration II — Final Polish

    Ultimate polishing step; ISO Class 5 aseptic fill performed in a validated laminar-flow workstation under full GMP-aligned conditions.

Performance vs. conventional media

By achieving a 0.04 µm final pore size across four sequential stages, FluxMPS™ delivers approximately 5× cleaner media by particulate count compared to single-pass 0.22 µm filtration, with full USP <788> compliance verified on every production lot.

Cleaner than conventional 0.22 µm media by particulate count
0.04
µm final filter pore size — sub-mycoplasma polishing
Sterility assurance: Every lot undergoes 14-day USP <71> sterility testing and USP <63>-equivalent mycoplasma assurance via sub-0.1 µm filtration. No bacterial or fungal growth observed.
FluxMPS™ CMRL 1066 Medium w/o Sodium Bicarbonate, Phenol Red: 1X Liquid (DCP-CMRL-BR1X) Quadruple-stage filtration system diagram showing four sequential stages: 0.1 μm Pre-filtration I, 0.04 μm Pre-filtration II, 0.1 μm Sterile-filtration I, and 0.04 μm Final Polish for organ-on-a-chip and microfluidic cell culture applications by Diagnocine
Figure 1. FluxMPS™ Quadruple-stage filtration architecture (0.1 µm ×2 + 0.04 µm ×2) delivering sub-mycoplasma purity for MPS and OoC applications.
© Diagnocine® — DCP-CMRL-BR1X
Applications

Designed for next-generation cell culture platforms

FluxMPS™ CMRL 1066 Medium w/o Sodium Bicarbonate, Phenol Red: 1X Liquid is validated for use across organ-on-a-chip, metabolic research, live-cell imaging, and primary cell models where particulate contamination and endotoxin variation are unacceptable.

Automated Bioreactors & Robotics

Next-Generation System Uptime

An optional 0.01 µm (10 nm) ultra-filtered variant is available for automated bioreactor and robotic perfusion systems requiring the ultimate particulate exclusion.

  • Total Particulate Exclusion: 10 nm filtration for nanoscale valve and sensor protection
  • Valve & Sensor Protection: prevents particulate-induced blockage in precision fluidic systems
  • Extended Perfusion Stability: maintains flow rate consistency across multi-week automated runs

Inquiry Required: The 0.01 µm grade is available by special order. Contact support@diagnocine.com to request this variant.

Microfluidics

Micro Physiological System (MPS) & Chip

Ultra-filtered formulation prevents microchannel clogging and maintains laminar flow integrity across complex chip geometries.

OoCToCBoCLoCMPS
Cancer Biology

Warburg Effect & Metabolic Research

Defined carbon source and low-endotoxin background enables precise metabolic flux analysis and Warburg effect studies.

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

iPSC-Derived Models

Ultrapure formulation supports sensitive iPSC differentiation protocols where endotoxin and particulates cause off-target effects.

iPSC-NeuronsiPSC-CMiPSC-Hep
Vascular Biology

Endothelial & Primary Cells

Microchannel-safe purity essential for maintaining endothelial barrier integrity and TEER values in perfusion models.

HUVECsHAECsPrimary hepatocytes
Metabolomics

Metabolic Flux Analysis

Chemically defined base enables isotope tracing experiments without interfering background metabolites.

13C tracingSeahorse XFNMR metabolomics
Live-Cell Imaging

Microscopy & Optical Sensing

Minimal autofluorescence and ultra-low particulate load ideal for high-content confocal imaging and optical biosensor integration.

ConfocalBiosensorsTEER
Technical Specifications

Lot-release quality parameters

Every production lot of FluxMPS™ CMRL 1066 Medium w/o Sodium Bicarbonate, Phenol Red: 1X Liquid undergoes the complete quality-release battery listed below before shipment.

Physical & Chemical Parameters
Parameter Specification
Formulation CMRL 1066 Medium w/o Sodium Bicarbonate, Phenol Red: 1X Liquid
Appearance Pale-Colorless, clear solution
pH USP <791> 7.4
Osmolality USP <785> Contact for specification
Glucose 1000 mg/L (1.0 g/L)
L-Glutamine 100 mg/L
Sodium Pyruvate Not present
Phenol Red Not Present
Sterility, Purity & Safety Parameters
Parameter Specification
Endotoxin USP <85> BET less than 0.05 EU/mL
Sterility USP <71> No growth after 14 days
Mycoplasma Controlled by 0.04 µm filter USP <63> equiv.
Particulate ≥10 µm USP <788> Compliant
Particulate ≥25 µm USP <788> Compliant
Water Purity USP <85> Ultrapure Type 1, 18.2 MΩ·cm
Manufacturing std. ISO 13485:2016 ISO 13485
Fill environment ISO Class 5 (Class 100)
Storage, Handling & Logistics
Parameter Specification
Storage temperature 2–8°C, protected from light
Freeze-thaw Not recommended
Shelf life 12 months from manufacture
Shipping condition cold pack
CO₂ requirement Yes, 5-10% CO₂
Raw Materials & Regulatory Traceability
Parameter Specification
Raw material grade Cell culture / reagent grade
Traceability Full lot documentation, CoA available
Manufacturing QMS ISO 13485:2016 certified
Regulatory alignment 21 CFR Part 820 (cGMP) aligned
Production method Micro-batch precision manufacturing
Intended use For Research Use Only (RUO)
Formulation

Full composition (mg/L)

Complete formulation with CAS numbers. All ingredient names and mg/L values are reproduced from the manufacturer specification. Custom compositions available on request.

Component CAS Number mg/L
INORGANIC SALTS
Calcium chloride dihydrate 10035-04-8 265.000
Magnesium sulphate anhydrous 7487-88-9 97.690
Potassium chloride 7447-40-7 400.000
Sodium acetate anhydrous 127-09-3 50.000
Sodium chloride 7647-14-5 6800.000
Sodium dihydrogen phosphate anhydrous 7558-80-7 122.000
Component CAS Number mg/L
AMINO ACIDS
Glycine 56-40-6 50.000
L-Alanine 56-41-7 25.000
L-Arginine 74-23-7 57.870
L-Aspartic acid 56-84-8 30.000
L-Cysteine hydrochloride monohydrate 7048-04-6 260.000
L-Cystine dihydrochloride 30189-89-0 20.000
L-Glutamic acid 56-86-0 75.000
L-Glutamine 56-85-9 100.000
L-Histidine hydrochloride monohydrate 5934-29-2 20.000
L-Isoleucine 73-32-5 20.000
L-Leucine 61-90-5 60.000
L-Lysine hydrochloride 657-27-2 70.000
L-Methionine 63-68-3 15.000
L-Phenylalanine 63-91-2 25.000
L-Proline 147-85-3 40.000
L-Serine 56-45-1 25.000
L-Threonine 72-19-5 30.000
L-Tryptophan 73-22-3 10.000
L-Tyrosine disodium salt dihydrate 69847-45-6 40.000
L-Valine 72-18-4 25.000
Trans-4-Hydroxy-L-Proline 51-35-4 10.000
Component CAS Number mg/L
VITAMINS
Choline chloride 67-48-1 0.500
D-Biotin 58-85-5 0.010
D-Pantothenate (Hemicalcium) 137-08-6 0.010
Folic acid 59-30-3 0.010
L-Ascorbic acid sodium salt 134-03-2 50.000
Nicotinamide 98-92-0 0.025
Nicotinic acid 59-67-6 0.025
Pyridoxal hydrochloride 65-22-5 0.025
Pyridoxine hydrochloride 58-56-0 0.025
Riboflavin 83-88-5 0.010
Thiamine hydrochloride 67-03-8 0.010
myo-Inositol 87-89-8 0.050
p-Amino benzoic acid (PABA) 150-13-0 0.050
OTHERS
2' Deoxyadenosine 958-09-8 10.000
2' Deoxycytidine hydrochloride 2' 960-71-4 10.000
Deoxyguanosine 961-07-9 10.000
5-Methyldeoxycytidine 838-07-3 0.100
Cholesterol 57-88-5 0.200
Cocarboxylase 154-87-0 1.000
Coenzyme A sodium salt 102029-73-2 2.500
D-Glucose 50-99-7 1000.000
D-Glucuronic acid sodium salt 207569-96-4 3.880
FAD disodium salt 84366-81-4 0.106
Glutathione reduced 70-18-8 10.000
Thymidine 50-89-5 10.000
Tween 80 9005-65-6 5.000
Uridine-5-Triphosphate.Na 19817-92-6 1.000
β-NAD 53-84-9 7.000
β-NADP sodium salt 1184-16-3 1.000
Customization: pH, glucose concentration, salt balance, HEPES concentration, and full nutrient profile are available on request. Contact support@diagnocine.com with your specifications.
Quality Assurance

ISO 13485:2016 manufacturing & compliance

FluxMPS™ CMRL 1066 Medium w/o Sodium Bicarbonate, Phenol Red: 1X Liquid is manufactured under a full ISO 13485:2016 quality management system, with final packaging, testing, and customization completed at DiagnoCine Precision in Totowa, New Jersey, USA.

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ISO 13485:2016 QMS

Full quality management system certification covering all manufacturing, testing, and release processes for every production lot.

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Ultrapure Type 1 Water

All media prepared with 18.2 MΩ·cm resistivity water meeting USP <85> Water for Injection standards — zero ionic interference.

biotech

ISO Class 5 Fill & Finish

Aseptic filling performed in validated laminar-flow (ISO Class 5 / Class 100) workstations; 21 CFR Part 820 cGMP aligned.

assignment

Micro-Batch Precision

Small-batch manufacturing locks in lot-to-lot nutrient consistency critical for reproducible perfusion studies and long-term OoC experiments.

Endotoxin — USP <85> BET

Limulus Amebocyte Lysate (LAL) test performed on every lot. Result: less than 0.05 EU/mL.

Particulate — USP <788> Method 2

Light obscuration particle count test confirms ≥10 µm and ≥25 µm particulate compliance on every lot.

Osmolality — USP <785>

Freezing-point osmometry performed per USP <785>. Result: Contact for specification.

Documentation — CoA & Full Lot Records

Certificate of Analysis available for every lot, including full QC panel, raw material traceability, and release signatures.

Certificate of Analysis: Request your lot-specific CoA at support@diagnocine.com with your lot number and order reference.
Product Comparison

How DCP-CMRL-BR1X (FluxMPS™) compares

Side-by-side comparison against conventional 0.22 µm-filtered alternatives of the same base formulation.

Parameter DCP-CMRL-BR1X (FluxMPS™) Conventional Click (0.22 µm) Standard Click alternative
Base Formulation CMRL 1066 Medium w/o Sodium Bicarbonate, Phenol Red: 1X Liquid Click Standard Click Equivalent
Final filtration pore size 0.04 µm 0.22 µm 0.22 µm
Number of filtration stages 4 stages 1 stage 1–2 stages
Mycoplasma barrier filtration check_circle cancel cancel
Endotoxin specification less than 0.05 EU/mL Typically less than 1 EU/mL Varies by lot
USP particulate compliance check_circle USP <788> cancel cancel
Water quality Ultrapure Type 1 (18.2 MΩ) Purified water Purified water
Manufacturing QMS ISO 13485:2016 Variable Variable
Microfluidic channel compatibility check_circle Validated cancel Risk of clogging cancel Risk of clogging
Custom formulation check_circle On request cancel Limited
FAQ

Frequently asked questions

Common questions about FluxMPS™ CMRL 1066 Medium w/o Sodium Bicarbonate, Phenol Red: 1X Liquid and MPS-grade cell culture media.

Yes. DCP-CMRL-BR1X is processed through our proprietary Quadruple-stage filtration (0.1 µm ×2 + 0.04 µm ×2), yielding ultra-low particulate counts that prevent microchannel clogging in OoC and MPS devices.
Standard 0.22 µm filtration leaves intact mycoplasma (0.1–0.3 µm diameter) and substantial subvisible particulates that accumulate inside microchannels. FluxMPS™ uses four sequential stages reaching 0.04 µm, removing these contaminants at the source and delivering approximately 5× lower particulate counts per USP <788>.
This formulation contains 1000 mg/L (1.0 g/L). If your cell type requires a different glucose level, contact support@diagnocine.com for a custom formulation with your preferred concentration. Supplement directly before use if needed for short-term experiments.
This formulation does not contain sodium bicarbonate. HEPES buffering provides pH stability without requiring a CO2 incubator, though standard CO2 conditions are still compatible.
Yes. FluxMPS™ CMRL 1066 Medium w/o Sodium Bicarbonate, Phenol Red: 1X Liquid can be supplemented with FBS (typically 5–20%), growth factors, antibiotics, or other additives per standard cell culture practice. Add supplements immediately before use. The ultra-clean base formulation minimizes background interference from supplement interactions.
Every production lot is tested by Limulus Amebocyte Lysate (LAL) assay per USP <85> BET. The release specification is less than 0.05 EU/mL. Lot-specific results are documented in the Certificate of Analysis available on request from support@diagnocine.com.
Yes. A lot-specific CoA is available for every shipment and includes: appearance, pH (USP <791>), osmolality (USP <785>), endotoxin (USP <85> BET), sterility (USP <71>), particulate matter (USP <788>), raw material traceability, manufacturing date, and authorized release signatures. Request via support@diagnocine.com.
Scientific References

Supporting literature

Peer-reviewed publications supporting the scientific rationale for MPS-grade ultra-filtered media and microfluidic cell culture applications.

  1. Huh D et al. (2010). Reconstituting organ-level lung functions on a chip. Science, 328(5986), 1662–1668. doi:10.1126/science.1188302
  2. Bhatia SN & Ingber DE (2014). Microfluidic organs-on-chips. Nature Biotechnology, 32(8), 760–772. doi:10.1038/nbt.2989
  3. Bhattacharya S et al. (2018). Challenges in maintaining cell viability during microfluidic experiments. Electrophoresis, 39(7), 997–1006. doi:10.1002/elps.201700375
  4. Warburg O (1956). On the origin of cancer cells. Science, 123(3191), 309–314. doi:10.1126/science.123.3191.309
  5. Emmons EV (1965). Detection of mycoplasma in cell cultures using filtration. Proceedings of the Society for Experimental Biology, 118, 1010–1015. doi:10.3181/00379727-118-29988
  6. Kim S et al. (2012). Gut-on-a-chip microdevice replicates key functional features of the human intestine. Lab on a Chip, 12(12), 2165–2174. doi:10.1039/c2lc40074j
  7. Zhang YS et al. (2017). Multisensor-integrated organs-on-chips platform for automated and continual in situ monitoring of organoid behaviors. PNAS, 114(12), E2293–E2302. doi:10.1073/pnas.1612906114
  8. Vernetti L et al. (2017). Functional coupling of human microphysiology systems. Scientific Reports, 7, 42296. doi:10.1038/srep42296
  9. Schuster B et al. (2020). Automated microfluidic platform for dynamic and combinatorial drug screening of tumor organoids. Nature Communications, 11, 5271. doi:10.1038/s41467-020-19058-4
  10. Zheng F et al. (2021). Organ-on-a-chip systems: microengineering to biomimic living systems. Small, 17(7), 2004175. doi:10.1002/smll.202004175

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