FluxMPS™ Ham's F-12 Nutrient Mixture, Coon's Modification w/o Sodium Bicarbonate: 2X Liquid

Product#: DCP-12C-B2X
$110.00
DCP-12C-B2X
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FluxMPS™ Ham's F-12 Nutrient Mixture, Coon's Modification w/o Sodium Bicarbonate: 2X Liquid

Double-strength (2X) Coon's modified Ham's F-12 — 4.0 g/L glucose in the concentrate, 2.0 g/L at 1X — for hybrid-cell culture, FRTL-5 and other rat thyroid cells, hormone-response and iodide-transport research and agarose culture, ultra-filtered through a quadruple-stage 0.1 µm / 0.04 µm filtration system. With a bicarbonate-free base for user-defined buffering, it is approximately 5× cleaner than conventional 0.22 µm-filtered media by particulate count.

  • 2X concentrate: mix with an equal volume of a compatible solution or matrix for a final 1X medium
  • Coon's modification: about twice the amino acids and sodium pyruvate of standard F-12, plus ascorbic acid and an adjusted salt composition
  • Quadruple-stage filtration: 0.1 µm membrane filtered twice, 0.04 µm membrane filtered twice
  • 0.04 µm nano-filtration final polish acts as a mycoplasma barrier
  • Endotoxin < 0.05 EU/mL (USP <85> BET)
  • Formulation: [+] 4.0 g/L Glucose, [+] L-Glutamine, [+] Sodium Pyruvate, [+] Phenol Red; [−] Sodium Bicarbonate, [−] HEPES
  • Ultrapure Type 1 water (18.2 MΩ·cm); ISO Class 5 (Class 100) aseptic fill in Totowa, NJ
  • Custom formulations available — pH, glucose, HEPES, salts, and nutrient composition on request
DCP-12C-B2X|UNSPSC 41116155Cell culture media
Catalog No. DCP-12C-B2X · Size: 500 mL
Ham's F-12 Nutrient Mixture, Coon's Modification w/o Sodium Bicarbonate: 2X Liquid
  • D-Glucose4,000 mg/L
  • L-Glutamine584 mg/L
  • Sodium Pyruvate440 mg/L
  • BufferNone (user-defined)
  • Phenol Red2.48 mg/L
  • AppearanceRed to Bright Pink
  • pH7.4 (± 0.04)
  • Endotoxin< 0.05 EU/mL
  • Filtration0.1 µm ×2 + 0.04 µm ×2
  • Format2X liquid, 500 mL
ISO 13485:2016USP <85> <785> <788>RUO
Why FluxMPS™

Engineered where standard media fails

Conventional Ham's F-12 is sterile-filtered once at 0.22 µm. That pore size can pass mycoplasma and leaves subvisible particulates that settle in microchannels, foul membranes and hydrogels, and add noise to optical readouts.[11,12] FluxMPS™ Ham's F-12 keeps Ham's formulation and removes that failure mode.

filter_alt

Microchannel-safe purity

A 0.04 µm final filter and USP <788> particulate control keep subvisible debris out of chips, tubing, membranes and matrices.

target

Total metabolic control

Defined 4,000 mg/L D-glucose, 584 mg/L L-glutamine and 440 mg/L sodium pyruvate in the 2X (half that at 1X).

water_drop

Ultrapure-grade water

Made with Ultrapure Type 1 water (18.2 MΩ·cm) and released at < 0.05 EU/mL endotoxin by USP <85>.

visibility

Low background for imaging

Particle-depleted medium reduces scatter and debris artifacts in colony counting, confocal imaging and on-chip sensing.

science

Matrix-ready 2X strength

49 components at double strength, so agar, hydrogels, supplements or treatment solutions can be added 1:1 without diluting the medium below 1X.

tune

Customization on demand

pH, glucose, HEPES, salts, and nutrient composition on request — contact support@diagnocine.com.

Purity Architecture

Quadruple-stage filtration system

Every lot of DCP-12C-B2X is membrane filtered at 0.1 µm twice and 0.04 µm twice — a ready-to-dilute 2X Ham's F-12 polished to a 0.04 µm final pore size, a purity level single-pass 0.22 µm media cannot reach.

  1. 01

    0.1 µmPre-filtration I

    Removes large particulates and aggregates and extends the life of the downstream filters.

  2. 02

    0.04 µmPre-filtration II

    Retains fine particulates, bacteria and mycoplasma.

  3. 03

    0.1 µmSterile-filtration I

    Second-pass redundancy that catches anything shed or bypassed upstream.

  4. 04

    0.04 µmSterile-filtration II — Final Polish

    Final nano-polish immediately before ISO Class 5 aseptic fill.

Performance vs. conventional media

By particulate count, FluxMPS™ Ham's F-12 is approximately 5× cleaner than conventional 0.22 µm-filtered media, lowering clog risk in narrow channels and long perfusion runs.

5×
cleaner by particulate count vs. 0.22 µm media
0.04
µm final filtration pore size
Sterility & mycoplasma assurance: no bacterial or fungal growth is observed after 14 days of incubation, as per USP specification (USP <71>), and the 0.04 µm stages provide USP <63>-equivalent mycoplasma assurance.[11]
FluxMPS™ Ham's F-12 Nutrient Mixture, Coon's Modification w/o Sodium Bicarbonate: 2X Liquid (DCP-12C-B2X) Quadruple-stage filtration system diagram: 0.1 μm pre-filtration, 0.04 μm pre-filtration, 0.1 μm sterile filtration and 0.04 μm final polish for MPS-grade Coon's modified F-12 cell culture media used in thyroid-cell, hybrid-cell, organ-on-a-chip and microfluidic applications, Diagnocine
Figure 1. Quadruple-stage filtration: 0.1 µm pre-filtration, 0.04 µm pre-filtration, 0.1 µm sterile filtration and 0.04 µm final polish before ISO Class 5 fill.
© Diagnocine® — DCP-12C-B2X
Applications

Where FluxMPS™ Coon's F-12 fits

Ham’s F-12 Nutrient Mixture, Coon’s Modification, is a modified basal medium for in vitro mammalian-cell research. Relative to standard Ham’s F-12, it contains approximately twice the amino-acid and sodium-pyruvate concentrations, includes ascorbic acid, and has an adjusted salt composition.[2] Originally developed for hybrid-cell culture, Coon’s modified F-12 is also used, with appropriate supplements, for rat thyroid cell lines such as FRTL-5.[1,3] It provides a basal nutrient environment for laboratory studies of cell growth, hormone responsiveness, and differentiated thyroid-cell functions.

Ham’s F-12 Nutrient Mixture, Coon’s Modification, 2X, is a double-strength version of the corresponding 1X Coon’s formulation, intended for laboratory workflows that dilute the basal medium during final preparation. Its purpose is dilution compensation, following the established use of 2X media in equal-volume mixtures with aqueous agar or agarose preparations.[4] Mixing one volume of 2X medium with one volume of a compatible solution that contributes none of its basal ingredients gives those ingredients at their intended 1X concentrations. The published agar/agarose methods establish this dilution principle, not the compatibility or performance of a specific 2X Coon’s product.

Important distinction: Ordinary 1X Coon’s modification already has approximately double the amino acids and pyruvate of standard F-12; that does not make it a 2X medium. “2X Coon’s” means twice the corresponding Coon’s formulation, not simply another name for standard-strength Coon’s modified F-12.

It is useful for:

  • Hybrid-cell culture research
  • Rat thyroid-cell culture
  • Hormone-response and cell-signaling research
  • Iodide-transport and thyroid-function research
  • Cell-based chemical-response studies
  • Chondrogenic differentiation research
  • Semisolid or agarose culture development

Automated Bioreactors & Robotics

Next-Generation System Uptime

For automated bioreactors, liquid-handling robots and closed perfusion loops with fine valves and in-line sensors, an optional 10 nm (0.01 µm) ultra-filtered grade of this medium is available.

  • Total Particulate Exclusion: 0.01 µm filtration removes virtually all particulates down to the nanometer scale.
  • Valve & Sensor Protection: keeps micro-valves, pumps and optical or electrochemical sensors free of deposits.
  • Extended Perfusion Stability: supports long, uninterrupted perfusion runs with fewer line changes.

Inquiry Required: the 0.01 µm grade is made on request — email support@diagnocine.com with your catalog number and volume.

Endocrinology

FRTL-5 & Rat Thyroid Cells

The basal medium for hormone-dependent FRTL-5 thyroid epithelial cells when supplemented with serum and a defined hormone mixture.[3]

FRTL-5ThyroidTSH response
Cell Genetics

Hybrid-Cell Culture

Coon's modification was developed for the formation and growth of viable somatic cell hybrids.[1]

Somatic hybridsCell fusionClonal growth
Physiology

Hormone Response & Iodide Transport

A basal environment for studying hormone responsiveness, cell signaling, iodide uptake and other differentiated thyroid-cell functions.[3]

Hormone responseIodide transportSignaling
Differentiation

Chondrogenic & Agarose Culture

A double-strength base for agarose and other semisolid preparations, including chondrogenic differentiation research.[4]

ChondrogenesisAgaroseSemisolid
Microfluidics

Organ-on-a-Chip & MPS

Microchannel-safe medium for perfused organ-, tissue- and body-on-a-chip platforms.[8,9,10]

OoCToCMPS
Live-Cell Imaging

Microscopy & Optical Sensing

Fewer particles means cleaner fields for colony counting, confocal imaging and on-chip biosensors.

ConfocalColony countingBiosensors
Technical Specifications

Specifications & quality control

Release specifications for DCP-12C-B2X. Lot-specific values are reported on the Certificate of Analysis.

Physical & Chemical Parameters
Parameter Specification
Formulation [+] 4.0 g/L Glucose, [+] L-Glutamine, [+] Sodium Pyruvate, [+] Phenol Red; [−] Sodium Bicarbonate, [−] HEPES
Concentration 2X (dilute 1:1 to 1X)
Appearance Red to Bright Pink
pH 7.4 (± 0.04) USP <791>
Osmolality Measured per lot; reported on CoA USP <785>
D-Glucose 4,000 mg/L (4.0 g/L; 2.0 g/L at 1X)
L-Glutamine 584 mg/L
Sodium Pyruvate 440 mg/L
Sodium Bicarbonate Not included
Phenol Red 2.48 mg/L
HEPES Not included
Sterility, Purity & Safety Parameters
Parameter Specification
Endotoxin < 0.05 EU/mL USP <85> BET
Sterility No bacterial or fungal growth after 14 days of incubation USP <71>
Mycoplasma 0.04 µm barrier filtration USP <63> equiv.
Particulate ≥10 µm Meets limits USP <788> M2
Particulate ≥25 µm Meets limits USP <788> M2
Water purity Ultrapure Type 1, 18.2 MΩ·cm
Manufacturing std. ISO 13485:2016 ISO
Fill environment ISO Class 5 (Class 100) ISO
Storage, Handling & Logistics
Parameter Specification
Storage temperature 2–8 °C, protected from light
Freeze-thaw Do not freeze
Shelf life 12 months; use before the expiry date on the product label
Shipping condition Ice Pack
CO₂ requirement Depends on the buffer you add; supply sodium bicarbonate before use in a CO₂ incubator
Raw Materials & Regulatory Traceability
Parameter Specification
Raw material grade High-purity, cell-culture-tested components
Traceability Lot-traceable; CoA per lot
Manufacturing QMS ISO 13485:2016 ISO
Regulatory alignment 21 CFR Part 820 (cGMP) aligned
Production method Micro-batch 2X liquid, quadruple-stage filtered; aseptic fill and finish in Totowa, NJ
Intended use For Research Use Only (RUO)
Note: pH and sodium bicarbonate concentration of the prepared medium are critical factors affecting cell growth. This is also influenced by amount of medium and volume of culture vessel used (surface to volume ratio). For example, in large bottles, such as Roux bottles, pH tends to rise perceptibly as a significant volume of carbon dioxide is released. Therefore, optimal conditions of pH, sodium bicarbonate concentration and surface to volume ratio must be determined for each cell type. We recommend stringent monitoring of pH. If needed, pH can be adjusted by using sterile 1N HCl or 1N NaOH or by bubbling in carbon dioxide. If required, supplements can be added to the medium prior to or after filter sterilization observing sterility precautions.
Formulation

Full composition (mg/L)

DCP-12C-B2X is 2X Coon's modified Ham's F-12 with 4.0 g/L glucose, L-glutamine, sodium pyruvate and Phenol Red. It does not contain sodium bicarbonate nor HEPES. Users are advised to review the literature for recommendations regarding medium supplementation and physiological growth requirements specific for different cell lines. All 49 components are listed below at 2X strength; values are per-lot release basis and are halved after 1:1 dilution.

Component CAS Number mg/L
INORGANIC SALTS
Calcium chloride dihydrate 10035-04-8 330.000
Copper sulphate pentahydrate 7758-99-8 0.0050
Disodium hydrogen phosphate anhydrous 7558-79-4 264.080
Ferrous sulphate heptahydrate 7782-63-0 1.668
Magnesium chloride hexahydrate 7791-18-6 212.000
Magnesium sulphate anhydrous 7487-88-9 101.600
Potassium chloride 7447-40-7 610.000
Potassium dihydrogen phosphate 7778-77-0 136.000
Sodium chloride 7647-14-5 15060.000
Zinc sulphate heptahydrate 7446-20-0 0.288
Component CAS Number mg/L
AMINO ACIDS
Glycine 56-40-6 32.000
L-Alanine 56-41-7 36.000
L-Arginine hydrochloride 1119-34-2 844.000
L-Asparagine anhydrous 70-47-3 60.000
L-Aspartic acid 56-84-8 52.000
L-Cysteine hydrochloride 52-89-1 140.520
L-Glutamic acid 56-86-0 60.000
L-Glutamine 56-85-9 584.000
L-Histidine hydrochloride monohydrate 5934-29-2 84.000
L-Isoleucine 73-32-5 15.600
L-Leucine 61-90-5 52.400
L-Lysine hydrochloride 657-27-2 146.000
L-Methionine 63-68-3 18.000
L-Phenylalanine 63-91-2 20.000
L-Proline 147-85-3 140.000
L-Serine 56-45-1 42.000
L-Threonine 72-19-5 47.600
L-Tryptophan 73-22-3 8.000
L-Tyrosine disodium salt 69847-45-6 31.720
L-Valine 72-18-4 46.800
Component CAS Number mg/L
VITAMINS
Biotin 58-85-5 0.0146
Choline chloride 67-48-1 27.920
D-Ca-Pantothenate 137-08-6 0.960
Folic acid 59-30-3 2.640
L-Ascorbic acid 50-81-7 90.000
Nicotinamide 98-92-0 0.080
Pyridoxine hydrochloride 58-56-0 0.120
Riboflavin 83-88-5 0.080
Thiamine hydrochloride 67-03-8 0.680
Vitamin B12 68-19-9 2.720
i-Inositol 87-89-8 36.040
OTHERS
D-Glucose 50-99-7 4000.000
Hypoxanthine sodium salt 45738-97-4 8.080
Linoleic acid 60-33-3 0.180
Lipoic acid 1077-28-7 0.412
Phenol Red 34487-61-1 2.480
Putrescine dihydrochloride 333-93-7 0.600
Sodium pyruvate 113-24-6 440.000
Thymidine 50-89-5 1.400
Customization: Custom formulations available — pH, glucose, HEPES, salts, and nutrient composition on request. Contact support@diagnocine.com.
Quality Assurance

Manufacturing & compliance

Manufactured under an ISO 13485:2016 quality management system; aseptic fill and finish in Totowa, NJ, with every lot released against compendial test methods.

verified

ISO 13485:2016 QMS

Documented, audited quality management system aligned with 21 CFR Part 820 (cGMP).

water_drop

Ultrapure Type 1 Water

18.2 MΩ·cm water as the formulation base for low ionic and endotoxin background.

biotech

ISO Class 5 Fill & Finish

Aseptic filling in an ISO Class 5 (Class 100) environment in Totowa, NJ, right after the final 0.04 µm polish.

assignment

Micro-Batch Precision

Small, tightly controlled batches for consistent composition and pH from lot to lot.

Endotoxin — USP <85> BET

Released at < 0.05 EU/mL.

Particulate — USP <788> Method 2

Subvisible particles ≥10 µm and ≥25 µm within compendial limits.

Osmolality — USP <785>

Measured per lot and reported on the CoA.

Documentation / CoA

Appearance, pH 7.4 (± 0.04), 14-day sterility, endotoxin and osmolality per lot.

A lot-specific Certificate of Analysis is available for every lot — request it at support@diagnocine.com.
Product Comparison

How DCP-12C-B2X compares

Same Ham's F-12 chemistry, different purity class. Conventional columns describe typical single-pass 0.22 µm-filtered catalog media.

Parameter DCP-12C-B2X (FluxMPS™) Conventional Coon's F-12, 1X (0.22 µm filtered) Conventional 2X Ham's F-12 (0.22 µm filtered)
Formulation 2X Coon's modified F-12; free of sodium bicarbonate 1X Coon's F-12, ready to use Double-strength, for semisolid culture
Final filtration pore size 0.04 µm 0.22 µm 0.22 µm
Number of filtration stages 4 1 1
Mycoplasma barrier filtration check_circle cancel cancel
Endotoxin specification < 0.05 EU/mL Often not specified at this level Often not specified at this level
USP <788> particulate compliance check_circle cancel cancel
Ultrapure Type 1 water (18.2 MΩ·cm) check_circle Varies Varies
ISO 13485:2016 manufacturing check_circle Varies Varies
Microfluidic channel compatibility check_circle cancel cancel
Custom formulation check_circle cancel cancel
FAQ

Frequently asked questions

Common questions about using DCP-12C-B2X for semisolid, 3D, microfluidic and conventional culture.

Yes. DCP-12C-B2X is quadruple-stage filtered to a 0.04 µm final pore size, so it carries far fewer subvisible particles than 0.22 µm media — approximately 5× cleaner by particulate count. That lowers the risk of clogging microchannels, valves and membranes in organ-on-a-chip, hydrogel-based 3D and microfluidic perfusion systems.[8,9,10]
The medium is filtered four times: 0.1 µm twice and 0.04 µm twice. A single 0.22 µm pass can let mycoplasma and fine particulates through; the 0.04 µm stages act as a mycoplasma barrier and polish out sub-micron particles before ISO Class 5 aseptic fill.[11]
Leaving sodium bicarbonate out lets the solution or matrix you mix with the 2X carry the buffer, or lets you set your own bicarbonate level for your CO₂ tension. Our complete 2X formulation carries 5,352 mg/L sodium bicarbonate (2,676 mg/L at 1X); pH and sodium bicarbonate concentration are critical to cell growth, so monitor pH closely. Users are advised to review the literature for supplementation and physiological growth requirements specific to each cell type.[1,3]
It depends on the buffer you add. With sodium bicarbonate, use a CO₂-controlled incubator; with a non-volatile buffer such as HEPES, CO₂ is not needed for pH control.
Mix one volume of 2X Coon's medium with one volume of a compatible solution that contributes none of its basal ingredients — for example aqueous agar or agarose — so glucose (2.0 g/L), amino acids, vitamins and salts end up at their 1X Coon's concentration.[4] Note that ordinary 1X Coon's already has about double the amino acids and pyruvate of standard F-12; that does not make it a 2X medium. Serum, antibiotics and other supplements can be added before or after filter sterilization, observing sterility precautions.
The endotoxin specification is < 0.05 EU/mL, tested by the USP <85> bacterial endotoxins test (BET) and reported on the lot Certificate of Analysis. The medium is made with Ultrapure Type 1 water (18.2 MΩ·cm).
Yes. Each lot ships with a CoA covering appearance (red to bright pink), pH 7.4 (± 0.04), sterility (no bacterial or fungal growth after 14 days of incubation per USP), endotoxin and osmolality results. Request copies at support@diagnocine.com.
Scientific References

Supporting literature

Peer-reviewed background on Coon's modified F-12, hybrid-cell and FRTL-5 thyroid culture, soft-agar culture, Phenol Red, organ-on-a-chip culture and mycoplasma control.

  1. Coon HG, Weiss MC. A quantitative comparison of formation of spontaneous and virus-produced viable hybrids. Proc Natl Acad Sci USA. 1969;62(3):852–859. doi:10.1073/pnas.62.3.852
  2. Ham RG. Clonal growth of mammalian cells in a chemically defined, synthetic medium. Proc Natl Acad Sci USA. 1965;53(2):288–293. doi:10.1073/pnas.53.2.288
  3. Ambesi-Impiombato FS, Parks LA, Coon HG. Culture of hormone-dependent functional epithelial cells from rat thyroids. Proc Natl Acad Sci USA. 1980;77(6):3455–3459. doi:10.1073/pnas.77.6.3455
  4. Borowicz S, Van Scoyk M, Avasarala S, et al. The soft agar colony formation assay. J Vis Exp. 2014;(92):e51998. doi:10.3791/51998
  5. Barnes D, Sato G. Methods for growth of cultured cells in serum-free medium. Anal Biochem. 1980;102(2):255–270. doi:10.1016/0003-2697(80)90151-7
  6. Morton HJ. A survey of commercially available tissue culture media. In Vitro. 1970;6(2):89–108. doi:10.1007/BF02616111
  7. Berthois Y, Katzenellenbogen JA, Katzenellenbogen BS. Phenol red in tissue culture media is a weak estrogen: implications concerning the study of estrogen-responsive cells in culture. Proc Natl Acad Sci USA. 1986;83(8):2496–2500. doi:10.1073/pnas.83.8.2496
  8. Bhatia SN, Ingber DE. Microfluidic organs-on-chips. Nat Biotechnol. 2014;32(8):760–772. doi:10.1038/nbt.2989
  9. Low LA, Mummery C, Berridge BR, Austin CP, Tagle DA. Organs-on-chips: into the next decade. Nat Rev Drug Discov. 2021;20(5):345–361. doi:10.1038/s41573-020-0079-3
  10. Leung CM, de Haan P, Ronaldson-Bouchard K, et al. A guide to the organ-on-a-chip. Nat Rev Methods Primers. 2022;2:33. doi:10.1038/s43586-022-00118-6
  11. Drexler HG, Uphoff CC. Mycoplasma contamination of cell cultures: incidence, sources, effects, detection, elimination, prevention. Cytotechnology. 2002;39(2):75–90. doi:10.1023/A:1022913015916
  12. Halldorsson S, Lucumi E, Gómez-Sjöberg R, Fleming RMT. Advantages and challenges of microfluidic cell culture in polydimethylsiloxane devices. Biosens Bioelectron. 2015;63:218–231. doi:10.1016/j.bios.2014.07.029

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