FluxMPS™ RPMI 1640 Medium (ATCC Modification): 1X Liquid

Product#: DCP-RPMIA1X
$52.80
DCP-RPMIA1X
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warning For Research Use Only (RUO). Not intended for clinical, diagnostic, or therapeutic use in humans.
verified ISO 13485 Certified Manufacturing

FluxMPS™ RPMI 1640 Medium (ATCC Modification): 1X Liquid

Contains L-Glutamine Contains Sodium Bicarbonate Contains Phenol Red Contains HEPES Contains Calcium Contains Magnesium Contains Glucose Contains Sodium Pyruvate

FluxMPS™ DCP-RPMIA1X is a Microfluidics Suitable, ultra-filtered RPMI 1640 (ATCC Modification) cell culture medium engineered for organ-on-a-chip (OoC) and microphysiological system (MPS) platforms. Processed through a Quadruple-stage filtration train (0.1 µm ×2 + 0.04 µm ×2, four validated passes), it reaches a 0.04 µm final polish well beyond conventional 0.22 µm–filtered media.

  • Endotoxin release specification < 0.05 EU/mL (LAL, USP <85>), tested every manufacturing batch
  • Quadruple-stage filtration train (0.1 µm ×2 + 0.04 µm ×2), four validated passes to a 0.04 µm final polish
  • ATCC-modified RPMI 1640 formulation: 4.5 g/L glucose, 2 mM L-glutamine, 1 mM sodium pyruvate, 1.5 g/L sodium bicarbonate, 10 mM HEPES and phenol red
  • Manufactured under an ISO 13485:2016 quality management system with full lot traceability
  • 41 verified ingredients per lot across inorganic salts, amino acids, vitamins and other components, each with CAS traceability
  • Formulated for 5% CO₂ incubation, consistent with its sodium bicarbonate buffering system
  • pH, glucose, HEPES, salts, and nutrient composition available on request — contact support@diagnocine.com
CAT. NO.
DCP-RPMIA1X | Cell culture media UNSPSC: 41116155 | Commodity: Molecular biology and cell culture growth media | (UNv260801)
RPMI 1640 Medium (ATCC Modification): 1X Liquid
  • Glucose4500.000 mg/L
  • L-Glutamine300.000 mg/L (≈2 mM)
  • Sodium Pyruvate110.000 mg/L (≈1 mM)
  • pH (USP <791>)7.4
  • Osmolality (USP <785>)Contact for specification
  • Endotoxin (USP <85>)< 0.05 EU/mL
  • Filtration0.1 µm ×2 + 0.04 µm ×2
  • Storage2–8°C, protect from light
  • Shelf Life12 months from date of manufacture, unopened
  • ShippingCold pack (insulated, gel packs)
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 confound sensitive on-chip and imaging assays.

filter_alt

Microchannel-safe purity

A 0.04 µm final filter and USP <788> particulate compliance help keep media particle-free for OoC microfluidic chips and narrow-bore channels.

target

Total metabolic control

A fully defined, quantified formulation — 4.5 g/L glucose, 2 mM glutamine, 1 mM pyruvate — gives precise control of carbon source and metabolic input for flux and Warburg-effect studies.

water_drop

Ultrapure-grade water

Type 1 water, 18.2 MΩ·cm resistivity (ASTM D1193 / ISO 3696), with tight trace-metal and organic-carbon (TOC) control at the point of formulation.

visibility

Low background for imaging

Ultra-low particulate baseline supports confocal, biosensor, and live-cell imaging applications on-chip.

science

Rich, stable nutrient profile

41 verified ingredients per lot, full CAS traceability, micro-batch precision manufacturing.

tune

Customization on demand

pH, nutrient concentrations, HEPES, and component modifications available. Contact support@diagnocine.com.

Purity Architecture

Quadruple-stage filtration system

Four serial filtration passes, run as two dedicated prefilter + final-filter pairs, reach a final 0.04 µm polish under aseptic fill conditions — well beyond the retention of conventional 0.22 µm–filtered media.

  1. 1

    0.1 µm Prefiltration I

    Removes large aggregates, cell debris and protein aggregates; protects the first 0.04 µm cartridge.

  2. 2

    0.04 µm Final filtration I

    First 0.04 µm pass; retains sub-micron particulates and microaggregates that a 0.22 µm filter allows through.

  3. 3

    0.1 µm Prefiltration II

    Second dedicated prefilter, protecting the second 0.04 µm cartridge and providing redundant particulate reduction.

  4. 4

    0.04 µm Final filtration II — Polish

    Ultimate polishing filter; aseptic fill & finish. Final product QC release gate.

Filtration architecture vs. conventional media

FluxMPS™ DCP-RPMIA1X runs a paired prefilter + final-filter train, twice in series, to a 0.04 µm final cut-off — a materially finer retention grade than standard 0.22 µm–filtered media.

0.04
µm final pore size — sub-mycoplasma polishing
4
validated filtration passes (0.1 µm ×2 + 0.04 µm ×2)
Sterility & Mycoplasma: No growth after 14-day incubation (USP <71>); mycoplasma control is by 0.1 µm mycoplasma-retentive filtration (not tested per lot). 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™ DCP-RPMIA1X RPMI 1640 (ATCC Modification) Quadruple-stage filtration system, 0.1 micron times 2 plus 0.04 micron times 2, for organ-on-a-chip and microfluidic cell culture media, Diagnocine
Figure 1. FluxMPS™ Quadruple-stage filtration system (0.1 µm ×2 + 0.04 µm ×2) — DCP-RPMIA1X.
© Diagnocine® — DCP-RPMIA1X
Applications

OoC and MPS Applications

FluxMPS™ DCP-RPMIA1X delivers Microfluidics Suitable, ultra-filtered purity for organ-on-a-chip, tissue-chip, and microfluidic applications.

Automated Bioreactors & Robotics

Next-Generation System Uptime

An optional 0.01 µm (10 nm) MPS Grade, ultra nano-filtered variant is available on request for automated bioreactors and robotic perfusion systems that demand the finest available cut-off.

  • Total Particulate Exclusion: 10 nm filtration removes nanoparticulate aggregates that foul automated systems
  • Valve & Sensor Protection: Reduces micro-fouling risk in automated perfusion and recirculation systems
  • Extended Perfusion Stability: Supports consistent nutrient delivery over long-duration culture runs

Inquiry Required: Contact support@diagnocine.com to request the 0.01 µm MPS Grade variant.

Microfluidics

Micro Physiological System (MPS) & Chip

0.04 µm-filtered media for organ-on-a-chip, tissue-on-a-chip, and body-on-a-chip platforms where particle-free media helps prevent channel fouling.

OoCToCBoCLoCMPS
Cancer Biology

Cancer Cell Lines & Metabolic Research

Supports RPMI-adapted cancer lines and Warburg-effect metabolic studies with precise, quantified nutrient control.

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

iPSC-Derived Models

Ultra-filtered base for iPSC differentiation protocols requiring defined, particulate-controlled media.

iPSC-NeuronsiPSC-CMiPSC-Hep
Vascular Biology

Endothelial & Primary Cells

Particle-controlled formulation for primary cells and endothelial monolayer studies on-chip.

HUVECsHAECsPrimary hepatocytes
Metabolomics

Metabolic Flux Analysis

Defined formulation for ¹³C isotope tracing and NMR metabolomics. Not compatible with Agilent Seahorse XF assays, which require bicarbonate-free, phenol red-free medium.

¹³C tracingNMR metabolomics
Live-Cell Imaging

Microscopy & Optical Sensing

Low particulate background supports confocal microscopy, biosensor measurements, and TEER monitoring on-chip.

ConfocalBiosensorsTEER
Technical Specifications

Analytical release specifications

Every lot released against the full specification matrix. Certificate of Analysis available: support@diagnocine.com.

Physical & Chemical Parameters
Parameter Specification
Formulation [+] L-Glutamine, [+] Sodium Bicarbonate, [+] Phenol Red, [+] HEPES, [+] Calcium, [+] Magnesium, [+] Glucose, [+] Sodium Pyruvate
Appearance Red-colored (phenol red indicator), clear solution
Total ingredients 41 components across 4 categories
pH USP <791> 7.4
Osmolality USP <785> Contact for specification
Glucose 4500.000 mg/L
L-Glutamine 300.000 mg/L
Sodium Pyruvate 110.000 mg/L
Phenol Red 5.300 mg/L (phenol red sodium salt)
Sterility, Purity & Safety Parameters
Parameter Specification
Endotoxin USP <85> BET < 0.05 EU/mL
Sterility USP <71> No growth / 14 days
Mycoplasma 0.1 µm mycoplasma-retentive filtration (not tested per lot)
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 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 date of manufacture, unopened
Shipping condition Cold pack
CO₂ requirement 5% CO₂ required (sodium bicarbonate-buffered formulation)
Raw Materials & Regulatory Traceability
Parameter Specification
Raw material grade Reagent / cell culture grade
Traceability Full lot traceability per ISO 13485
Manufacturing QMS ISO 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, per-lot QC release
Intended use Research Use Only (RUO)
Formulation

Full composition (mg/L)

RPMI 1640 Medium (ATCC Modification): 1X Liquid — 41 ingredients verified per lot with CAS numbers for full raw-material traceability. Pack sizes: 500 mL, 1000 mL.

Component CAS Number mg/L
INORGANIC SALTS
Calcium nitrate tetrahydrate 13477-34-4 100.000
Magnesium sulfate anhydrous 7487-88-9 48.840
Potassium chloride 7447-40-7 400.000
Sodium bicarbonate 144-55-8 1500.000
Sodium chloride 7647-14-5 6000.000
Sodium phosphate dibasic anhydrous 7558-79-4 800.000
Component CAS Number mg/L
AMINO ACIDS
Glycine 56-40-6 10.000
L-Arginine hydrochloride 1119-34-2 241.000
L-Asparagine 70-47-3 50.000
L-Aspartic acid 56-84-8 20.000
L-Cystine dihydrochloride 30925-07-6 65.200
L-Glutamic acid 56-86-0 20.000
L-Glutamine 56-85-9 300.000
L-Histidine hydrochloride monohydrate 5934-29-2 20.960
L-Hydroxyproline 51-35-4 20.000
L-Isoleucine 73-32-5 50.000
L-Leucine 61-90-5 50.000
L-Lysine hydrochloride 657-27-2 40.000
L-Methionine 63-68-3 15.000
L-Phenylalanine 63-91-2 15.000
L-Proline 147-85-3 20.000
L-Serine 56-45-1 30.000
L-Threonine 72-19-5 20.000
L-Tryptophan 73-22-3 5.000
L-Tyrosine Disodium Salt 69847-45-6 28.830
L-Valine 72-18-4 20.000
Component CAS Number mg/L
VITAMINS
Choline chloride 67-48-1 3.000
D-Biotin 58-85-5 0.200
D-Ca-Pantothenate 137-08-6 0.250
Folic acid 59-30-3 1.000
Niacinamide 98-92-0 1.000
Pyridoxine hydrochloride 58-56-0 1.000
Riboflavin 83-88-5 0.200
Thiamine hydrochloride 67-03-8 1.000
i-Inositol 87-89-8 35.000
p-Amino benzoic acid (PABA) 150-13-0 1.000
OTHERS
D-Glucose 50-99-7 4500.000
Glutathione reduced 70-18-8 1.000
HEPES 7365-45-9 2383.000
Phenol red sodium salt 34487-61-1 5.300
Sodium Pyruvate 113-24-6 110.000
Customization available: pH, glucose, HEPES, salts, and nutrient composition modifications available on request. Contact support@diagnocine.com.
Quality Assurance

ISO 13485 Manufacturing & Compliance

Every batch of FluxMPS™ DCP-RPMIA1X is manufactured under a certified ISO 13485:2016 QMS with full lot traceability and multi-parameter QC release testing.

verified

ISO 13485:2016 QMS

Full quality management system with documented procedures, deviation control, and CAPA. Every lot traceable from raw material to final release.

water_drop

Ultrapure Type 1 Water

18.2 MΩ·cm resistivity feed water with tight trace-metal and TOC control at the manufacturing source.

biotech

ISO Class 5 Fill & Finish

Final aseptic filling in ISO Class 5 (Class 100) cleanroom conditions. Immediate post-filtration fill to reduce recontamination risk.

assignment

Micro-Batch Precision

Small-batch manufacturing with per-lot QC release. Every batch tested independently — not pooled or blended across lots.

Endotoxin USP <85> BET

LAL-based endotoxin test per batch. Release specification: < 0.05 EU/mL; assay sensitivity 0.005 EU/mL.

Particulate USP <788> Method 1

Light obscuration particulate count. NMT 25/mL at ≥10 µm; NMT 3/mL at ≥25 µm.

Osmolality USP <785>

Verified per lot using vapor pressure or freezing-point depression osmometry per USP <785>.

Documentation / CoA

Full Certificate of Analysis available per lot, including all QC parameters, test dates, and raw material lot numbers. Request: support@diagnocine.com.

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-RPMIA1X compares

FluxMPS™ versus conventional 0.22 µm filtered media for OoC and MPS applications.

Parameter DCP-RPMIA1X (FluxMPS™) Conventional 0.22 µm Filtered Standard Alternative
Grade Microfluidics Suitable Not specified Not specified
Formulation 4.5g/L Glucose, 2mM L-Glutamine, 1mM Sodium Pyruvate, 1.5g/L NaHCO₃, HEPES, Phenol Red Standard RPMI 1640 Standard RPMI 1640
Final filtration pore size 0.04 µm 0.22 µm 0.22 µm
Number of filtration stages 4 passes 1 pass 1–2 passes
Mycoplasma barrier 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)
USP particulate compliance check_circle cancel cancel
Water quality Type 1, 18.2 MΩ·cm Type 2 typical Type 2 typical
Manufacturing QMS ISO 13485:2016 ISO 9001 typical Not specified
Microfluidic channel compatibility check_circle cancel cancel
Custom formulation check_circle cancel Limited

Comparison figures from published supplier specifications, accessed 2 September 2026. Suppliers that publish no numeric endotoxin specification are shown as "Not specified".

FAQ

Frequently asked questions

Common questions about FluxMPS™ DCP-RPMIA1X and its use in OoC and MPS applications.

Yes. DCP-RPMIA1X is engineered for MPS and OoC platforms. Its 0.04 µm final filtration helps prevent microfluidic channel fouling, making it suitable for OoC, ToC, BoC, and LoC applications with sensitivity to particulate contamination.
FluxMPS uses a Quadruple-stage filtration train (0.1 µm ×2 + 0.04 µm ×2), reaching a 0.04 µm final cut-off with 0.1 µm mycoplasma-retentive filtration — both finer than the 0.22 µm grade used in conventional media.
This is the ATCC-modified RPMI 1640 formulation: 4.5 g/L glucose, 2 mM L-glutamine, 1 mM sodium pyruvate, 1.5 g/L sodium bicarbonate, 10 mM HEPES, and phenol red. All standard carbon sources and buffering components are already present; most protocols only need serum or defined supplements added at time of use.
Yes. The 1.5 g/L sodium bicarbonate buffering system is formulated for 5% CO₂ incubation to help maintain a physiological pH near 7.4. Incubate at 37°C with 5% CO₂ unless your protocol specifies otherwise.
Yes. This is a basal medium formulation. Supplement with FBS, serum replacements (e.g., B27, N2), or growth factors as required by your cell type and protocol. When adding serum or protein-containing supplements, filter through a 0.2 µm low-protein-binding PES or PVDF membrane; do not use a 0.04 µm membrane for supplements, as it will strip serum proteins and clog quickly.
Endotoxin is released at < 0.05 EU/mL, verified by a LAL (Limulus Amebocyte Lysate) assay per USP <85> Bacterial Endotoxins Test, with an assay sensitivity of 0.005 EU/mL. Endotoxin is controlled and tested per manufacturing batch rather than per individual unit.
Yes. A CoA is available per lot upon request at support@diagnocine.com. It includes pH, osmolality, endotoxin, sterility, mycoplasma filtration status, USP <788> particulate data, appearance, and full raw material lot traceability.
Scientific References

Supporting literature

Curated peer-reviewed references relevant to OoC and MPS applications and FluxMPS™ ultra-filtered cell culture media.

  1. Bhatia SN, Ingber DE. Microfluidic organs-on-chips. Nature Biotechnology. 2014;32(8):760–772.doi:10.1038/nbt.2989
  2. Sackmann EK, Fulton AL, Beebe DJ. The present and future role of microfluidics in biomedical research. Nature. 2014;507(7491):181–189.doi:10.1038/nature13118
  3. Huh D, et al. Reconstituting organ-level lung functions on a chip. Science. 2010;328(5986):1662–1668.doi:10.1126/science.1188302
  4. Ingber DE. Is it time for Reviewer 3 to request human organ chip experiments instead of animal validation studies? Advanced Science. 2020;7(22):2002162.doi:10.1002/advs.202002162
  5. Maoz BM, et al. A linked organ-on-chip model of the human neurovascular unit reveals the metabolic landscape of brain disease. Nature Biotechnology. 2018;36:865–874.doi:10.1038/nbt.4226
  6. Bhise NS, et al. A liver-on-a-chip platform with bioprinted hepatic spheroids. Biofabrication. 2016;8(1):014101.doi:10.1088/1758-5090/8/1/014101
  7. Luni C, Serena E, Elvassore N. Human-on-chip for therapy development and fundamental science. Current Opinion in Biotechnology. 2014;25:45–50.doi:10.1016/j.copbio.2013.08.015
  8. Erickson KA, Bhansali S. Mycoplasma contamination in cell cultures: a survey of incidence and approaches to prevention. Journal of the Association for Laboratory Automation. 2012;17(5):346–354.doi:10.1177/2211068212456089
  9. van Duinen V, et al. Microfluidic 3D cell culture: from tools to tissue models. Current Opinion in Biotechnology. 2015;35:118–126.doi:10.1016/j.copbio.2015.05.002
  10. Warburg O. On the origin of cancer cells. Science. 1956;123(3191):309–314.doi:10.1126/science.123.3191.309

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