FluxMPS™ Nutrient Mixture F-12 Ham, Coon’s Modification w/ Sodium bicarbonate 1X Liquid Cell Culture Medium

Product#: DCP-F12HCM1X
$52.10
DCP-F12HCM1X
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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™ Nutrient Mixture F-12 Ham, Coon’s Modification w/ Sodium bicarbonate 1X Liquid Cell Culture Medium

Contains L-Glutamine Contains Sodium Bicarbonate Contains Phenol Red Contains Calcium Contains Magnesium Contains Glucose (2.0 g/L) Contains Sodium Pyruvate

FluxMPS™ DCP-F12HCM1X is a Microfluidics Suitable, ultra-filtered Nutrient Mixture F-12 Ham, Coon’s Modification formulation engineered for microphysiological systems (MPS), organ-on-a-chip (OoC), and microfluidic tissue models. A quadruple-stage train (0.1 µm ×2 + 0.04 µm ×2) reaches a 0.04 µm final cut-off, five times finer than the 0.22 µm membranes used for conventional sterile filtration. Formulation: L-Glutamine, Sodium Bicarbonate, Phenol Red, Calcium, Magnesium, D-Glucose (2.0 g/L), Sodium Pyruvate.

  • Ham’s F-12 Coon’s Modification with elevated amino acids, sodium pyruvate, and added L-ascorbic acid for demanding hybrid-cell fusion and CHO culture protocols
  • Formulation: L-Glutamine, Sodium Bicarbonate, Phenol Red, Calcium, Magnesium, D-Glucose (2.0 g/L), Sodium Pyruvate
  • Quadruple-stage sequential filtration — 0.1 µm Prefiltration I → 0.04 µm Final filtration I → 0.1 µm Prefiltration II → 0.04 µm Final filtration II — reaching a 0.04 µm final pore size
  • Endotoxin release specification < 0.05 EU/mL (LAL, USP <85>), controlled per manufacturing batch
  • Sodium bicarbonate–buffered (2676 mg/L); CO₂ requirement derived from bicarbonate concentration — approximately 7% CO₂ to maintain pH 7.4
  • Manufactured under an ISO 13485:2016 quality management system; final QC at Diagnocine, Totowa, NJ
  • 50 verified ingredients across four composition categories with full lot traceability
  • Custom pH, salts, and nutrient adjustments available on request
SKU: DCP-F12HCM1X Size: 500 mL and 1000 mL Cell Culture Media UNSPSC: 41116155 | Commodity: Molecular biology and cell culture growth media | (UNv260801)
Nutrient Mixture F-12 Ham, Coon’s Modification w/ Sodium bicarbonate 1X Liquid Cell Culture Medium
  • FormulationL-Glutamine, Sodium Bicarbonate, Phenol Red, Calcium, Magnesium, D-Glucose (2.0 g/L), Sodium Pyruvate
  • AppearancePink-Red colored, clear solution
  • pH (USP <791>)7.4
  • Osmolality (USP <785>)Contact for specification
  • Endotoxin (USP <85>)< 0.05 EU/mL
  • Sterility (USP <71>)No growth / 14 days
  • Filtration0.1 µm ×2 + 0.04 µm ×2
  • Total ingredients50
  • Storage2–8°C, away 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 passes mycoplasma-sized organisms, subvisible particulates, and endotoxin-bearing debris that clog microfluidic channels and corrupt sensor signals. FluxMPS™ addresses 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 supports safe perfusion across common chip geometries.

target

Total metabolic control

Selective inclusion of glutamine, pyruvate, and sodium bicarbonate for precise nutrient and buffer definition.

water_drop

Ultrapure-grade water

Ultrapure Type 1 water (18.2 MΩ·cm) for controlled trace-metal and organic-carbon (TOC) background.

visibility

Low background for imaging

Ultra-low particulate baseline from 0.04 µm final filtration reduces background scatter for confocal microscopy and optical biosensor platforms.

science

Rich, stable nutrient profile

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

tune

Customization on demand

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

Purity Architecture

Quadruple-stage filtration system

Four serial filtration stages, run as two dedicated prefilter + final-filter pairs, reach a final 0.04 µm polish under ISO Class 5 aseptic conditions — delivering sub-mycoplasma-grade particulate control beyond what conventional 0.22 µm filtration achieves.

  1. 1

    0.1 µm Prefiltration I — Large Particulate Removal

    Removes large aggregates, 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 through a standard 0.22 µm filter.

  3. 3

    0.1 µm Prefiltration II

    Second dedicated prefilter protecting the second 0.04 µm cartridge, providing full redundancy across the train.

  4. 4

    0.04 µm Final filtration II — Polish

    Ultimate polishing filter prior to aseptic fill and finish under ISO Class 5 (Class 100) conditions.

Performance vs. conventional media

4
Sequential 0.1 µm + 0.04 µm filtration passes
0.04
µm final pore size — sub-mycoplasma-grade polishing
Sterility & Mycoplasma: No growth after 14-day incubation (USP <71>). Mycoplasma risk is controlled by 0.1 µm mycoplasma-retentive filtration applied across the train (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 DCP-F12HCM1X Nutrient Mixture F-12 Ham, Coon's Modification w/ Sodium Bicarbonate 1X Liquid Cell Culture Medium - Quadruple-stage filtration system: 0.1 micron Prefiltration I, 0.04 micron Final filtration I, 0.1 micron Prefiltration II, 0.04 micron Final filtration II Polish - Microfluidics Suitable cell culture media for organ-on-a-chip and microphysiological system applications | Diagnocine
Figure 1. FluxMPS™ Quadruple-stage filtration system (0.1 µm ×2 + 0.04 µm ×2) used in production of DCP-F12HCM1X, reaching a 0.04 µm final pore size for microfluidic and organ-on-a-chip applications.
© Diagnocine® — DCP-F12HCM1X
Applications

Designed for next-generation cell models

FluxMPS™ DCP-F12HCM1X supports demanding platforms from single-channel microfluidic chips to multi-organ body-on-a-chip systems, as well as classical hybrid-cell and CHO culture work.

Automated Bioreactors & Robotics

Next-Generation System Uptime

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

  • Total Particulate Exclusion: 10 nm filtration removes nanoparticulate aggregates
  • Valve & Sensor Protection: Reduces micro-fouling risk for 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 MPS Grade variant.

Microfluidics

Micro Physiological System (MPS) & Chip

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

OoCToCBoCLoCMPS
Bioproduction

CHO & Mammalian Cell Culture

Elevated amino acid and sodium pyruvate levels support CHO, hybrid, and primary cell clonal growth protocols.

CHOMCF-7HeLaHEK293
Stem Cell Biology

iPSC-Derived Models

Ultra-low endotoxin (< 0.05 EU/mL) and 0.1 µm mycoplasma-retentive filtration support sensitive iPSC-derived protocols.

iPSC-NeuronsiPSC-CMiPSC-Hep
Vascular Biology

Endothelial & Primary Cells

Particulate-controlled, endotoxin-specified media for HUVEC monolayer integrity and TEER monitoring.

HUVECsHAECsPrimary hepatocytes
Metabolomics

Metabolic Flux Analysis

Defined, elevated-pyruvate formulation provides a consistent background for 13C isotope tracing and NMR-based metabolomics workflows. Not compatible with Agilent Seahorse XF assays, which require bicarbonate-free, phenol red-free medium.

13C tracingNMR metabolomics
Live-Cell Imaging

Microscopy & Optical Sensing

Ultra-low particulate baseline from 0.04 µm final filtration supports confocal microscopy 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 L-Glutamine, Sodium Bicarbonate, Phenol Red, Calcium, Magnesium, D-Glucose (2.0 g/L), Sodium Pyruvate
Appearance Pink-Red colored, clear solution
pH USP <791> 7.4
Osmolality USP <785> Contact for specification
Glucose 2.0 g/L (2000 mg/L)
L-Glutamine 292 mg/L
Sodium Pyruvate 220 mg/L
Phenol Red 1.240 mg/L (phenol red sodium salt)
Sterility, Purity & Safety
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> Method 1 NMT 25/mL
Particulate ≥25 µm USP <788> Method 1 NMT 3/mL
Water purity Ultrapure 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 date of manufacture, unopened
Shipping condition Cold pack
CO₂ requirement Approximately 7% CO₂ (derived from 2676 mg/L sodium bicarbonate to maintain pH 7.4)
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
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)

50 ingredients verified per lot with CAS numbers for full raw-material traceability. Ham’s F-12 Coon’s Modification carries zinc, putrescine, hypoxanthine and thymidine in addition to standard amino acids and vitamins, with doubled amino acid and pyruvate levels plus added ascorbic acid versus standard Ham’s F-12.

Component CAS Number mg/L
INORGANIC SALTS
Calcium chloride dihydrate 10035-04-8 165.000
Copper sulfate pentahydrate 7758-99-8 0.0025
Disodium hydrogen phosphate anhydrous 7558-79-4 132.040
Ferric sulfate heptahydrate 7782-63-0 0.834
Magnesium chloride hexahydrate 7791-18-6 106.000
Magnesium sulfate anhydrous 7487-88-9 50.800
Potassium chloride 7447-40-7 305.000
Potassium dihydrogen phosphate 7778-77-0 68.000
Sodium bicarbonate 144-55-8 2676.000
Sodium chloride 7647-14-5 7530.000
Zinc sulfate heptahydrate 7446-20-0 0.144
Component CAS Number mg/L
AMINO ACIDS
Glycine 56-40-6 16.000
L-Alanine 56-41-7 18.000
L-Arginine hydrochloride 1119-34-2 422.000
L-Asparagine anhydrous 70-47-3 30.000
L-Aspartic acid 56-84-8 26.000
L-Cysteine hydrochloride 52-89-1 70.260
L-Glutamic acid 56-86-0 30.000
L-Glutamine 56-85-9 292.000
L-Histidine hydrochloride monohydrate 5934-29-2 42.000
L-Isoleucine 73-32-5 7.800
L-Leucine 61-90-5 26.200
L-Lysine hydrochloride 657-27-2 73.000
L-Methionine 63-68-3 9.000
L-Phenylalanine 63-91-2 10.000
L-Proline 147-85-3 70.000
L-Serine 56-45-1 21.000
L-Threonine 72-19-5 23.800
L-Tryptophan 73-22-3 4.000
L-Tyrosine disodium salt dihydrate 69847-15-0 15.860
L-Valine 72-18-4 23.400
Component CAS Number mg/L
VITAMINS
Biotin 58-85-5 0.0073
Choline chloride 67-48-1 13.960
D-Ca-Pantothenate 137-08-6 0.480
Folic acid 59-30-3 1.320
L-Ascorbic acid 50-81-7 45.000
Nicotinamide 98-92-0 0.040
Pyridoxine hydrochloride 58-56-0 0.060
Riboflavin 83-88-5 0.040
Thiamine hydrochloride 67-03-8 0.340
Vitamin B12 68-19-9 1.360
i-Inositol 87-89-8 18.020
OTHERS
D-Glucose 50-99-7 2000.000
Hypoxanthine sodium salt 45738-97-4 4.040
Linoleic acid 60-33-3 0.090
Lipoic acid 1077-28-7 0.206
Phenol red sodium salt 34487-61-1 1.240
Putrescine dihydrochloride 333-93-7 0.300
Sodium pyruvate 113-24-6 220.000
Thymidine 50-89-5 0.700
Custom formulation: Contact support@diagnocine.com for DCP-F12HCM1X 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 an ISO 13485:2016 quality management system. Final QC at Diagnocine R&D Center, Totowa, NJ, USA.

water_drop

Ultrapure Type 1 Water

18.2 MΩ·cm resistivity Type 1 water, controlled for trace metals and organic carbon (TOC).

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 specification < 0.05 EU/mL per batch.

Particulate — USP <788> Method 1

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

Osmolality — USP <785>

Freezing-point osmometry. Target: Contact for specification.

Documentation & CoA

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

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.
Certificate of Analysis: Request for any DCP-F12HCM1X lot at support@diagnocine.com.
Product Comparison

How DCP-F12HCM1X compares

FluxMPS™ DCP-F12HCM1X vs. conventional 0.22 µm–filtered Ham’s F-12 Coon’s Modification formulations.

Parameter DCP-F12HCM1X (FluxMPS™) Conventional Ham’s F-12 Coon’s Mo
(0.22 µm filtered)
Standard Alt.
(0.22 µm filtered)
Grade Microfluidics Suitable (0.04 µm final) Not graded (0.22 µm filtered) Not graded (0.22 µm filtered)
Coon’s Modification — doubled amino acids and pyruvate plus ascorbic acid for hybrid cell culture 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-retentive filtration (0.1 µm) check_circle Yes cancel No cancel No
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 <788> Method 1 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 Microfluidics Suitable cancel Risk of clogging cancel Risk of clogging
Custom formulation check_circle Available cancel Fixed cancel Fixed

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™ DCP-F12HCM1X.

Yes. DCP-F12HCM1X is processed through a Quadruple-stage filtration system reaching a 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.
 
Coon’s Modification doubles amino acid and sodium pyruvate concentrations versus original F-12 and adds ascorbic acid, originally developed to optimize viable hybrid formation. The elevated nutrient levels support demanding cell fusion and hybrid selection protocols.
Yes. This formulation contains 2676 mg/L sodium bicarbonate. Based on the Henderson–Hasselbalch relationship, maintaining a pH of 7.4 at this bicarbonate concentration requires approximately 7% CO₂, rather than the 5% commonly associated with lower-bicarbonate formulations.
Yes. Add FBS (typically 5–10%), serum-free supplements, growth factors, antibiotics, or custom nutrients as required. Filter serum-containing additions through a 0.2 µm low-protein-binding PES or PVDF membrane before addition; the medium’s own 0.04 µm final filtration is not suitable for serum re-filtration. Contact support@diagnocine.com for custom co-formulation.
Endotoxin is controlled per manufacturing batch rather than per unit. Every batch is tested by LAL assay (USP <85> Bacterial Endotoxins Test; assay sensitivity 0.005 EU/mL) and must meet the release specification of < 0.05 EU/mL before release. A Certificate of Analysis is available on request.
Yes. A full CoA per lot covers: appearance, pH (USP <791>), osmolality (USP <785>), sterility (USP <71>), endotoxin (USP <85>), mycoplasma filtration status, particulate count (USP <788> Method 1), and raw-material traceability. Request at support@diagnocine.com.
Scientific References

Supporting literature

Key peer-reviewed publications supporting Microfluidics Suitable, ultra-filtered media in organ-on-a-chip and microfluidic research, and the underlying Ham’s F-12 Coon’s Modification formulation.

  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, McKeehan WL. Development of improved media and culture conditions for clonal growth of normal diploid cells. In Vitro. 1978;14:11–22. doi:10.1007/BF02618171
  4. Coon HG, Weiss MC. A quantitative comparison of formation of spontaneous and virus-produced viable hybrids. Proc Natl Acad Sci USA. 1969;62:852–859. doi:10.1073/pnas.62.3.852
  5. 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
  6. 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
  7. Schimek K, et al. Integrating biological vasculature into a multi-organ-chip microsystem. Lab Chip. 2013;13:3588–3598. doi:10.1039/c3lc50217a
  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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