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

Product#: DCP-CMRL-R1X
$64.90
DCP-CMRL-R1X
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warning For Research Use Only (RUO). Not intended for clinical, diagnostic, or therapeutic use in humans.
ISO 13485 Certified Manufacturing

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

Contains L-Glutamine Contains Sodium Bicarbonate Contains Calcium Contains Magnesium Contains Glucose Without Phenol Red Without HEPES Without Sodium Pyruvate

FluxMPS™ CMRL 1066 Medium w/o Phenol Red: 1X Liquid is a Microfluidics Suitable, quadruple-stage ultra-filtered (0.1 µm ×2 + 0.04 µm ×2) 1X liquid cell culture medium engineered for organ-on-a-chip (OoC), tissue-on-a-chip (ToC), and microphysiological system (MPS) applications. Processed through Diagnocine’s four-stage filtration train reaching a 0.04 µm final pore size, this phenol red-free CMRL 1066 formulation is built for microchannel-safe performance in imaging and biosensor-integrated culture platforms.

  • Quadruple-stage nano-filtration: 0.1 µm (Prefiltration I & II) + 0.04 µm (Final filtration I & II), reaching a 0.04 µm terminal pore size
  • Endotoxin release specification: < 0.05 EU/mL (USP <85> BET), controlled per manufacturing batch
  • CMRL 1066 base formulation, phenol red-free; 1000 mg/L (1.0 g/L) glucose and 100 mg/L L-glutamine
  • Sodium bicarbonate-buffered (2200 mg/L); requires approximately 5.8% CO₂ for physiological pH maintenance
  • Prepared with Ultrapure Type 1 water (18.2 MΩ·cm); ISO Class 5 aseptic fill & finish
  • Manufactured under an ISO 13485:2016 quality management system; final QC and customization completed at Diagnocine, Totowa, NJ
  • Custom formulations available — pH, glucose, salts, HEPES, and nutrient composition on request
DCP-CMRL-R1X | Cell Culture Media UNSPSC: 41116155 | Commodity: Molecular biology and cell culture growth media | (UNv260801)
CMRL 1066 Medium w/o Phenol Red: 1X Liquid · Available sizes: 500 mL, 1000 mL
  • Glucose1000 mg/L (1.0 g/L)
  • L-Glutamine100 mg/L
  • Sodium PyruvateNone / Not added
  • Phenol RedNone / Not added
  • pH (USP <791>)7.4
  • Osmolality (USP <785>)300 - 340 mOsm/kg H2O
  • Endotoxin (USP <85>)< 0.05 EU/mL
  • Filtration0.1 µm ×2 + 0.04 µm ×2 (4 stages)
  • Storage2–8°C, protect from light
  • Shelf Life12 months from date of manufacture, unopened
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 (0.2–0.3 µm), subvisible debris, and batch-to-batch endotoxin variability that accumulate inside microchannels — corrupting biosensor readings, stressing primary cultures, and shortening device lifetimes. FluxMPS™ is built around a four-stage 0.04 µm filtration train to address these failure modes directly.

filter_alt

Microchannel-safe purity

0.04 µm final filter stage retains particles down to sub-mycoplasma size; USP <788> Method 1 particulate compliance verified per lot.

target

Total metabolic control

Fixed 1000 mg/L glucose and 100 mg/L L-glutamine support standard metabolic workflows, with custom carbon-source and nutrient concentrations available for flux-based studies.

water_drop

Ultrapure-grade water

Prepared with Type 1 water (18.2 MΩ·cm), meeting ASTM D1193 Type I / ISO 3696 purity standards, with strict trace-metal and total organic carbon (TOC) control.

visibility

Low background for imaging

Phenol red-free, ultra-low particulate baseline supports confocal microscopy, live-cell biosensors, and TEER measurements without interference from filtration debris. Note: riboflavin (0.010 mg/L) contributes intrinsic fluorescence; account for it when configuring optical assays.

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.

tune

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 Phenol Red: 1X Liquid is processed through a four-stage serial filtration sequence that reaches a 0.04 µm final pore size — addressing mycoplasma-sized particulates and subvisible debris that 0.22 µm filtration alone cannot remove.

  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 from breakthrough.

  4. 4

    0.04 µm Final filtration II — Polish

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

Performance vs. conventional media

The train runs two dedicated 0.1 µm prefilter + 0.04 µm final-filter pairs in series, reaching a 0.04 µm terminal pore size with full USP <788> Method 1 (light obscuration) particulate compliance verified on every production lot.

4
Sequential filtration stages (2 prefilter + 2 final-filter pairs)
0.04
µm final filter pore size — sub-mycoplasma polishing
Sterility assurance: Every lot undergoes 14-day USP <71> sterility testing; no bacterial or fungal growth is observed during the incubation period. Mycoplasma risk is mitigated by 0.1 µm mycoplasma-retentive final-stage filtration (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™ CMRL 1066 Medium w/o Phenol Red: 1X Liquid (DCP-CMRL-R1X) Quadruple-stage filtration system diagram showing four sequential stages: 0.1 micron Prefiltration I, 0.04 micron Final filtration I, 0.1 micron Prefiltration II, and 0.04 micron Final filtration II 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 microfluidics-suitable purity for MPS and OoC applications.
© Diagnocine® — DCP-CMRL-R1X
Applications

Designed for next-generation cell culture platforms

FluxMPS™ CMRL 1066 Medium w/o Phenol Red: 1X Liquid is suited for organ-on-a-chip, imaging, and primary/stem cell models where particulate contamination, endotoxin variation, and phenol red interference are unacceptable.

Automated Bioreactors & Robotics

Next-Generation System Uptime

An optional 0.01 µm (10 nm) ultra nano-filtered MPS Grade variant — a separate product line from this Microfluidics Suitable formulation — is available for automated bioreactor and robotic perfusion systems requiring the highest 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 MPS Grade variant is available by special order. Contact support@diagnocine.com to request this variant.

Microfluidics

Micro Physiological System (MPS) & Chip

Ultra-filtered formulation reduces microchannel clogging risk and supports laminar flow integrity across complex chip geometries.

OoCToCBoCLoCMPS
Cancer Biology

Cell Line Maintenance & Metabolic Studies

Defined 1000 mg/L glucose base and low-endotoxin background support reproducible cancer cell line culture and downstream metabolic assays.

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 supports endothelial barrier integrity and TEER measurement stability in perfusion models.

HUVECsHAECsPrimary hepatocytes
Metabolomics

Metabolic Flux Analysis

Defined, reproducible base composition supports isotope tracing and NMR-based metabolomics workflows. Not compatible with Agilent Seahorse XF assays, which require bicarbonate-free, phenol red-free medium formulated to the XF specification.

13C tracingNMR metabolomics
Live-Cell Imaging

Microscopy & Optical Sensing

Phenol red-free, ultra-low particulate load supports confocal imaging and optical biosensor integration; account for intrinsic riboflavin fluorescence when designing assays.

ConfocalBiosensorsTEER
Technical Specifications

Lot-release quality parameters

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

Physical & Chemical Parameters
Parameter Specification
Formulation CMRL 1066 base + L-Glutamine + Sodium Bicarbonate + Calcium + Magnesium + Glucose; without Phenol Red, HEPES, Sodium Pyruvate
Appearance Pale yellow, clear solution (phenol red-free)
pH USP <791> 7.4
Osmolality USP <785> 300 - 340 mOsm/kg H2O
Glucose 1000 mg/L (1.0 g/L)
L-Glutamine 100 mg/L
Sodium Pyruvate None / Not added
Phenol Red None / Not added
Sterility, Purity & Safety Parameters
Parameter Specification
Endotoxin USP <85> BET < 0.05 EU/mL (batch release specification)
Sterility USP <71> No growth after 14 days
Mycoplasma 0.1 µm mycoplasma-retentive filtration (not tested per lot)
Particulate ≥10 µm USP <788> Compliant (Method 1, light obscuration)
Particulate ≥25 µm USP <788> Compliant (Method 1, light obscuration)
Water Purity 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 date of manufacture, unopened
Shipping condition Cold pack
CO₂ requirement Approximately 5.8% CO₂ (derived from 2200 mg/L NaHCO₃ buffering at pH 7.4; verify per incubator)
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
UNSPSC 41116155 — Molecular biology and cell culture growth media (UNv260801)
Regulatory alignment 21 CFR Part 820 (QMSR) aligned
Production method Micro-batch precision manufacturing
Intended use For Research Use Only (RUO)
Formulation

Full composition (mg/L)

Complete formulation with CAS numbers, reproduced from the manufacturer specification. 57 ingredient rows across 4 category groups. Custom compositions available on request.

Component CAS Number mg/L
INORGANIC SALTS
Calcium chloride dihydrate 10035-04-8 265.000
Magnesium sulfate anhydrous 7487-88-9 97.690
Potassium chloride 7447-40-7 400.000
Sodium acetate anhydrous 127-09-3 50.000
Sodium bicarbonate 144-55-8 2200.000
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
p-Amino benzoic acid (PABA) 150-13-0 0.050
OTHERS
myo-Inositol 87-89-8 0.050
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 Phenol Red: 1X Liquid is manufactured under a full ISO 13485:2016 quality management system, with final packaging, testing, and customization completed at Diagnocine in Totowa, New Jersey, USA.

verified

ISO 13485:2016 QMS

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

water_drop

Ultrapure Type 1 Water

Media prepared with 18.2 MΩ·cm resistivity water meeting ASTM D1193 Type I / ISO 3696 purity standards, with strict trace-metal and total organic carbon (TOC) control.

biotech

ISO Class 5 Fill & Finish

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

LAL assay performed per batch; assay sensitivity 0.005 EU/mL. Release specification: < 0.05 EU/mL.

Particulate — USP <788> Method 1

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: 300 - 340 mOsm/kg H2O.

Documentation — CoA & Full Lot Records

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

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 at support@diagnocine.com.
Product Comparison

How DCP-CMRL-R1X (FluxMPS™) compares

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

Parameter DCP-CMRL-R1X (FluxMPS™) Conventional CMRL (0.22 µm) Standard CMRL alternative
Grade Microfluidics Suitable Standard grade (0.22 µm) Standard grade (0.22 µm)
Base Formulation CMRL 1066 w/o Phenol Red CMRL Standard CMRL 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 (release specification) < 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 particulate compliance check_circle USP <788> Method 1 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

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™ CMRL 1066 Medium w/o Phenol Red: 1X Liquid.

Yes. DCP-CMRL-R1X is processed through Diagnocine's Quadruple-stage filtration (0.1 µm ×2 + 0.04 µm ×2), yielding a low particulate baseline that reduces microchannel clogging risk in OoC and MPS devices.
Standard 0.22 µm filtration does not retain mycoplasma-sized particles (0.2–0.3 µm diameter) or subvisible debris that accumulate inside microchannels. FluxMPS™ uses four sequential stages reaching 0.04 µm, with USP <788> Method 1 (light obscuration) particulate compliance verified on every production lot.
Phenol red is omitted to eliminate optical interference in colorimetric, fluorescence, and biosensor-based assays. This formulation already contains 1000 mg/L glucose and 100 mg/L L-glutamine; if your protocol requires HEPES buffering or sodium pyruvate, contact support@diagnocine.com for a custom formulation rather than supplementing components already balanced in the base medium.
Yes. This formulation is buffered with 2200 mg/L sodium bicarbonate, which requires approximately 5.8% CO₂ (derived via Henderson-Hasselbalch at pH 7.4) to maintain physiological pH. Verify empirically for your specific incubator and vessel geometry.
Yes. FluxMPS™ CMRL 1066 Medium w/o Phenol Red: 1X Liquid can be supplemented with FBS, growth factors, antibiotics, or other additives per standard cell culture practice. When adding serum or protein-containing supplements, filter through a 0.2 µm low-protein-binding PES or PVDF membrane (never 0.04 µm, which retains serum lipoproteins). Add supplements immediately before use.
Endotoxin is controlled per manufacturing batch, not per unit. Every batch is tested by LAL assay per USP <85> BET (assay sensitivity 0.005 EU/mL) and must meet the release specification of < 0.05 EU/mL before release. Batch-specific results are documented in the Certificate of Analysis available from support@diagnocine.com.
Yes. A batch-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> Method 1), 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 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. 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
  5. 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
  6. 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
  7. Vernetti L et al. (2017). Functional coupling of human microphysiology systems. Scientific Reports, 7, 42296. doi:10.1038/srep42296
  8. 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
  9. Zheng F et al. (2021). Organ-on-a-chip systems: microengineering to biomimic living systems. Small, 17(7), 2004175. doi:10.1002/smll.202004175
  10. Parham MB (1963). Studies on the composition of CMRL 1066 medium. Annals of the New York Academy of Sciences, 139, 132–144. doi:10.1111/j.1749-6632.1961.tb18994.x

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