FluxMPS™ Medium 199 w/ Earle’s salts and 25mM HEPES buffer w/o Sodium Pyruvate: 1X Liquid

Product#: DCP-M199H-P1X
$48.75
DCP-M199H-P1X
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verified ISO 13485 Certified Manufacturing

FluxMPS™ Medium 199 w/ Earle's salts and 25 mM HEPES buffer w/o Sodium Pyruvate: 1X Liquid

FluxMPS™ DCP-M199H-P1X is a MPS-grade formulation of the historically significant Medium 199 — the first nutritionally defined cell culture medium — enhanced for organ-on-a-chip (OoC), primary cell culture, vaccine production, and microfluidic platforms. Manufactured with Quadruple-stage filtration (0.1 µm ×2 + 0.04 µm ×2) and ISO Class 5 aseptic fill, it delivers endotoxin < 0.05 EU/mL and approximately 5× fewer subvisible particulates than conventional 0.22 µm-filtered Media 199.

  • Quadruple-stage nano-filtration: 0.1 µm ×2 pre-filtration + 0.04 µm ×2 sterile final polish
  • Endotoxin < 0.05 EU/mL (USP <85> BET verified)
  • Low Glucose 1,000 mg/L + L-Glutamine + NaHCO₃ + 25 mM HEPES + Earle's Salts; no Sodium Pyruvate
  • Ultrapure Type 1 water (18.2 MΩ·cm, USP <85>)
  • ISO Class 5 (Class 100) aseptic fill & finish
  • ISO 13485:2016 QMS & 21 CFR Part 820 (cGMP) aligned
  • Microchannel-safe: USP <788> Method 2 particulate compliant
  • pH 7.4 maintained with dual buffer system (NaHCO₃ + 25 mM HEPES)
Cat. No.
DCP-M199H-P1X | UNSPSC 12161503 Cell Culture Media
Medium 199 w/ Earle's salts and 25 mM HEPES w/o Sodium Pyruvate — 1X Liquid
  • Formulation[+] Low Glucose [+] L-Gln [+] NaHCO₃ [+] 25mM HEPES [+] Earle's Salts [−] Pyruvate
  • Glucose1,000 mg/L (Low Glucose)
  • L-Glutamine100.000 mg/L
  • Sodium PyruvateNot included
  • pH (USP <791>)7.4 at 1X
  • Osmolality (USP <785>)285.00–325.00 mOsm/kg H₂O
  • 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 manufacture
ISO 13485:2016 USP <85> <785> <788> RUO
Why FluxMPS™

Engineered where standard media fails

Conventional 0.22 µm-filtered Medium 199 harbors subvisible particulates, residual mycoplasma-sized debris (<0.2 µm), and endotoxin that corrupt primary cell behavior, distort vaccine production yields, and clog microfluidic channels in OoC and MPS platforms. FluxMPS™ DCP-M199H-P1X resolves these failure modes through a four-barrier filtration architecture and micro-batch ISO Class 5 production.

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Microchannel-Safe Purity

0.04 µm final barrier removes particulates that accumulate in organ-on-a-chip and microfluidic channels. USP <788> particulate compliance verified on every micro-batch lot.

target

Defined Metabolic Control

Low glucose (1,000 mg/L) with 25 mM HEPES supports primary cells, non-transformed lines, and vaccine production without the CO₂-dependency burden of bicarbonate-only buffering.

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Ultrapure Type 1 Water

All formulation uses 18.2 MΩ·cm water (USP <85>). Eliminates trace-ion interference in electrophysiology, TEER measurements, and biosensor-based OoC readouts.

visibility

Low Background for Imaging

Ultra-low particulate count minimizes autofluorescence in confocal, widefield, and TIRF microscopy, and reduces optical noise in inline chip biosensors.

science

Rich, Stable Nutrient Profile

Medium 199's comprehensive formulation — including nucleotides, vitamins, nucleosides, HEPES, and Earle's salts — supports demanding primary and non-transformed cell culture with micro-batch consistency.

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Customization On Demand

Sodium pyruvate, glucose concentration, HEPES level, and other nutrients adjustable on request. Contact support@diagnocine.com.

Purity Architecture

Quadruple-stage filtration system

FluxMPS™ DCP-M199H-P1X is the only ready-to-use Medium 199 available at 0.04 µm final filtration purity. Four sequential membrane barriers alternating 0.1 µm and 0.04 µm create an unmatched particulate and mycoplasma exclusion stack impossible to replicate with single-pass 0.22 µm filtration.

  1. 1

    0.1 µm Pre-filtration I

    Removes large particulates and aggregates. Protects downstream 0.04 µm membranes from premature fouling, maintaining pore integrity and consistent flow rates across the batch.

  2. 2

    0.04 µm Pre-filtration II

    Retains fine particulates, bacteria, and mycoplasma (smallest species ≈0.2 µm). Primary mycoplasma barrier essential for long-term primary cell culture, virus propagation, and MPS applications.

  3. 3

    0.1 µm Sterile-filtration I

    Second-pass 0.1 µm redundancy for sterility assurance per USP <71> 14-day specifications. Eliminates any trace contaminants that might bypass stage 2.

  4. 4

    0.04 µm Sterile-filtration II — Final Polish

    Ultimate polish under ISO Class 5 laminar-flow conditions. Delivers the ultra-clean, sub-mycoplasma final product that defines FluxMPS™ media performance.

Performance vs. conventional media

Independent particulate counting (USP <788> Method 2) demonstrates FluxMPS™ Medium 199 achieves approximately 5× lower subvisible particle burden than standard 0.22 µm-filtered Media 199. This directly reduces channel occlusion, attenuates innate immune activation in primary cell assays, and improves signal fidelity in biosensor-equipped chip systems.

Cleaner than 0.22 µm media by particulate count (USP <788>)
0.04
µm final filtration — industry-leading purity for ready-to-use Medium 199
Mycoplasma Assurance: 14-day USP <71> sterility testing plus USP <63>-equivalent mycoplasma assay confirm freedom from contamination on every production lot. The 0.04 µm barrier physically excludes all known mycoplasma species.
FluxMPS™ Medium 199 Earle Salts 25mM HEPES without Sodium Pyruvate DCP-M199H-P1X ? Quadruple-stage 0.1μm×2+0.04μm×2 ultra-filtered MPS-grade cell culture medium for organ-on-a-chip and microfluidic applications by Diagnocine
Figure 1. FluxMPS™ Quadruple-Stage Filtration System: two 0.1 µm pre-filtration stages followed by two 0.04 µm sterile-filtration stages, culminating in ISO Class 5 aseptic fill.
© Diagnocine® — DCP-M199H-P1X
Applications

Validated applications for FluxMPS™ Medium 199

Originally developed by Morgan, Morton, and Parker (1950), Medium 199 remains the gold standard for primary cell nutrition. FluxMPS™ DCP-M199H-P1X extends this heritage to MPS, OoC, and microfluidic platforms requiring endotoxin-controlled, particulate-free media.

Automated Bioreactors & Robotics

Next-Generation System Uptime

For automated perfusion bioreactors and robotic liquid-handling systems, an optional 0.01 µm (10 nm) ultra-filtered variant of FluxMPS™ Medium 199 is available on inquiry. This grade eliminates nano-aggregates that foul precision valve seats, inline optical sensors, and pump mechanisms.

  • Total Particulate Exclusion: 10 nm filtration removes aggregates invisible to 0.04 µm membranes, protecting sensitive automation hardware.
  • Valve & Sensor Protection: Ultra-clean media extends service intervals of solenoid valves, bubble detectors, and inline optical sensors in automated systems.
  • Extended Perfusion Stability: Consistent, particulate-free perfusion maintains primary cell viability over multi-week continuous culture without media-induced occlusion.

Inquiry Required: The 0.01 µm grade is manufactured on request. Contact support@diagnocine.com for volume, lead time, and pricing.

Microfluidics

Micro Physiological System (MPS) & Chip

Particulate-free Medium 199 for epithelial, endothelial, and primary cell chip models. HEPES buffering enables stable pH in open microfluidic environments.

OoC ToC BoC LoC MPS
Virology

Vaccine & Virus Production

Medium 199's original design for primary chick embryo fibroblasts makes it the standard for vaccine research. FluxMPS™ purity enhances viral yield reproducibility.

Chick embryo fibroblasts Vero Primary explants
Stem Cell Biology

iPSC-Derived & Primary Cell Models

Endotoxin-controlled Medium 199 supports primary explants of epithelial cells and iPSC-derived models requiring a defined nutritional environment.

iPSC-derived Primary epithelial Non-transformed cells
Vascular Biology

Endothelial & Primary Cells

Endotoxin <0.05 EU/mL prevents NF-κB activation artifacts in endothelial monolayer and vascular chip studies. Earle's salts provide physiological ionic environment.

HUVECs HAECs Primary hepatocytes
Metabolomics

Metabolic Flux Analysis

Low glucose (1,000 mg/L) and absence of sodium pyruvate enable precise isotope-traced metabolic flux experiments without confounding exogenous pyruvate carbon.

¹³C tracing Seahorse XF NMR metabolomics
Live-Cell Imaging

Microscopy & Optical Sensing

Ultra-low particulate background minimizes autofluorescence artifacts in confocal, biosensor, and TEER-based chip imaging applications.

Confocal Biosensors TEER
Technical Specifications

Complete technical specifications

All specifications are per-lot verified. Certificate of Analysis (CoA) available on request at support@diagnocine.com.

Physical & Chemical Parameters
Parameter Specification
Formulation [+] Low Glucose [+] L-Gln [+] NaHCO₃ [+] 25mM HEPES [+] Earle's Salts [−] Na Pyruvate
Appearance Orange to Red-colored, clear liquid
pH (USP <791>) 7.4 at 1X concentration USP <791>
Osmolality (USP <785>) 285.00–325.00 mOsm/kg H₂O USP <785>
Glucose 1,000 mg/L (Low Glucose)
L-Glutamine 100.000 mg/L
Sodium Pyruvate Not included
Phenol Red Included (15 mg/L, disodium salt)
Sterility, Purity & Safety Parameters
Parameter Specification
Endotoxin (USP <85> BET) < 0.05 EU/mL USP <85>
Sterility (USP <71>) No growth after 14 days incubation USP <71>
Mycoplasma Negative (USP <63> equivalent assay)
Particulate ≥10 µm (USP <788>) Compliant USP <788>
Particulate ≥25 µm (USP <788>) Compliant USP <788>
Water purity Ultrapure Type 1, 18.2 MΩ·cm USP <85>
Manufacturing std. ISO 13485:2016 ISO 13485
Fill environment ISO Class 5 (Class 100) laminar flow
Storage, Handling & Logistics
Parameter Specification
Storage temperature 2–8 °C, protect from bright light
Freeze-thaw Do not freeze
Shelf life 12 months from manufacture date
Shipping condition Cold pack (2–8 °C)
CO₂ requirement 5% CO₂ recommended (dual buffered: NaHCO₃ + 25 mM HEPES)
Raw Materials & Regulatory Traceability
Parameter Specification
Raw material grade Analytical / USP-grade reagents
Traceability Full lot traceability per ISO 13485
Manufacturing QMS ISO 13485:2016 certified ISO 13485
Regulatory alignment 21 CFR Part 820 (cGMP) aligned
Production method Micro-batch aseptic manufacturing
Intended use Research Use Only (RUO)
Formulation

Full composition (mg/L)

Medium 199 is one of the most complex defined media, originally formulated for nutritional studies in primary chick embryo fibroblasts. All values are per-lot release targets confirmed on the CoA.

Component CAS Number mg/L
INORGANIC SALTS
Calcium chloride dihydrate 10035-04-8 265.000
Ferric nitrate nonahydrate 7782-61-8 0.720
Magnesium sulphate anhydrous 7487-88-9 97.720
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 phosphate monobasic 10049-21-5 122.000
Component CAS Number mg/L
AMINO ACIDS
Glycine 56-40-6 50.000
L-Alanine 56-41-7 25.000
L-Arginine hydrochloride 1119-34-2 70.000
L-Aspartic acid 56-84-8 30.000
L-Cysteine hydrochloride monohydrate 7048-04-6 0.100
L-Cystine dihydrochloride 30925-07-6 26.000
L-Glutamic acid 56-86-0 67.000
L-Glutamine 56-85-9 100.000
L-Histidine hydrochloride monohydrate 5934-29-2 22.000
L-Hydroxyproline 51-35-4 10.000
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 69847-44-5 57.660
L-Valine 72-18-4 25.000
Component CAS Number mg/L
VITAMINS
Ascorbic acid 50-81-7 0.050
Calciferol 50-14-6 0.100
Choline chloride 67-48-1 0.500
D-Biotin 58-85-5 0.010
D-Ca-Pantothenate 137-08-6 0.010
DL-Tocopherol phosphate 5765-44-6 0.010
Folic acid 59-30-3 0.010
Menadione 58-27-5 0.010
Niacinamide 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
Retinol Acetate 127-47-9 0.140
Riboflavin 83-88-5 0.010
Thiamine hydrochloride 67-03-8 0.010
i-Inositol 87-89-8 0.050
p-Amino benzoic acid (PABA) 150-13-0 0.050
OTHERS
Adenine sulphate 321-30-2 10.000
Adenosine triphosphate 987-65-5 1.000
Adenosine monophosphate 61-19-8 0.200
Cholesterol 57-88-5 0.200
Deoxyribose 533-67-5 0.500
Glucose 50-99-7 1000.000
Glutathione reduced 70-18-8 0.050
Guanine hydrochloride 635-39-2 0.300
HEPES Buffer 7365-45-9 5958.000
Hypoxanthine sodium salt 5765-44-6 0.354
Phenol red disodium salt 34487-61-1 15.000
Polysorbate 80 9005-65-6 4.900
Ribose 50-69-1 0.500
Thymine 65-71-4 0.300
Uracil 66-22-8 0.300
Xanthine 69-89-6 0.344
Customization available: Sodium pyruvate, glucose concentration, HEPES concentration, and other nutrients can be adjusted on request. Contact support@diagnocine.com with your requirements.
Quality Assurance

Manufacturing & compliance overview

Every FluxMPS™ Medium 199 lot is manufactured under a fully auditable ISO 13485:2016 quality management system with complete raw-material traceability, multi-barrier sterility, and third-party endotoxin verification.

verified

ISO 13485:2016 QMS

Manufacturing conducted under ISO 13485-certified and CE-approved facilities (Diagnocine Precision suppliers). All final QA, testing, and packaging at the DiagnoCine R&D and Quality Testing Center, Totowa, New Jersey, USA.

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Ultrapure Type 1 Water

All formulation uses 18.2 MΩ·cm (resistivity) water meeting USP <85> specifications. This eliminates ionic contamination interfering with electrophysiology and chip-based biosensors.

biotech

ISO Class 5 Fill & Finish

Aseptic filling inside ISO Class 5 (Class 100) laminar-flow enclosures, ensuring particulate and bioburden levels consistent with injectable-grade manufacturing standards.

assignment

Micro-Batch Precision

Small-batch production enables per-batch QC verification, tighter lot-to-lot consistency, and faster turnaround for custom formulation requests. Each batch individually tested and released.

Endotoxin — USP <85> BET

Limulus Amebocyte Lysate (LAL) test on every lot. Release criterion: < 0.05 EU/mL, exceeding standard cell-culture requirements.

Particulate — USP <788> Method 2

Light-obscuration particle counting verifies ≤10 µm and ≤25 µm particulate limits, confirming microchannel-safe purity on every production lot.

Osmolality — USP <785>

Freezing-point depression osmometry per USP <785>. Specification: 285.00–325.00 mOsm/kg H₂O. Lot-specific values on CoA.

Documentation & CoA

Full Certificate of Analysis including pH, osmolality, endotoxin, sterility, and particulate data for every lot. Request via support@diagnocine.com.

CoA Availability: Certificate of Analysis for each lot available on request. Email support@diagnocine.com with your lot number.
Product Comparison

How DCP-M199H-P1X compares

FluxMPS™ Medium 199 versus conventional 0.22 µm and 0.1 µm filtered alternatives.

Parameter DCP-M199H-P1X (FluxMPS™) Conventional Medium 199 (0.22 µm) Standard Medium 199 (0.1 µm)
Distinctive formulation 25 mM HEPES + Earle's Salts; no Pyruvate Variable; often includes pyruvate Variable
Final filtration pore size 0.04 µm 0.22 µm 0.1 µm
Number of filtration stages 4 stages 1 stage 1–2 stages
Mycoplasma barrier filtration check_circle cancel check_circle
Endotoxin specification < 0.05 EU/mL Not specified / > 1 EU/mL Not standardized
USP particulate compliance check_circle USP <788> cancel cancel
Water quality Ultrapure 18.2 MΩ·cm Purified water Purified water
Manufacturing QMS ISO 13485:2016 Standard GMP Standard GMP
Microfluidic channel compatibility check_circle cancel Partial
Custom formulation check_circle Limited Limited
FAQ

Frequently asked questions

Common questions about FluxMPS™ DCP-M199H-P1X performance, compatibility, and ordering.

Yes. FluxMPS™ DCP-M199H-P1X is engineered for OoC and MPS platforms. The 0.04 µm final filtration prevents channel clogging, and the endotoxin specification (<0.05 EU/mL) prevents TLR4-mediated artifacts in primary cell chip assays. The 25 mM HEPES also provides stable pH in open microfluidic environments.
Four sequential membranes (0.1 µm, 0.04 µm, 0.1 µm, 0.04 µm) yield approximately 5× lower particulate count and physical mycoplasma exclusion versus single-pass 0.22 µm filtration, verified by USP <63>-equivalent mycoplasma assay and USP <788> particulate testing.
DCP-M199H-P1X omits sodium pyruvate to enable precise isotope-traced metabolic flux analysis without confounding exogenous pyruvate carbon. For cell types requiring pyruvate supplementation, add it exogenously or request a custom formulation with a defined pyruvate concentration via support@diagnocine.com.
The medium contains both sodium bicarbonate (2,200 mg/L) and 25 mM HEPES buffer. The HEPES provides CO₂-independent buffering capacity, while sodium bicarbonate works optimally with 5% CO₂. For fully CO₂-free systems, HEPES-only formulations are available on request.
Yes. Medium 199 is widely used with serum supplementation (typically 5–10% FBS) for growth of diverse cell types. For primary cells and long-term non-transformed cell maintenance, serum is generally required. The medium is compatible with standard growth factors, antibiotics, and supplements.
Every lot of DCP-M199H-P1X is tested by Limulus Amebocyte Lysate (LAL) assay per USP <85> Bacterial Endotoxins Test (BET). Release criterion: < 0.05 EU/mL. The lot-specific endotoxin value is documented on the Certificate of Analysis available on request.
Yes. A Certificate of Analysis is available for every production lot. It includes: pH (USP <791>), osmolality (USP <785> ? 285–325 mOsm/kg H₂O), appearance, endotoxin (USP <85>), sterility (USP <71> 14-day), mycoplasma status, and particulate count (USP <788>). Request via support@diagnocine.com with your lot number.
Scientific References

Supporting literature

Curated peer-reviewed references supporting Medium 199 use in primary cells, virus production, microfluidic platforms, and organ-on-a-chip applications.

  1. Morgan JF, Morton HJ, Parker RC. Nutrition of animal cells in tissue culture. I. Initial studies on a synthetic medium. Proc Soc Exp Biol Med. 1950;73(1):1–8. doi:10.3181/00379727-73-17557
  2. Bhatia SN, Ingber DE. Microfluidic organs-on-chips. Nat Biotechnol. 2014;32(8):760–772. doi:10.1038/nbt.2989
  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. Ramzy PI, et al. Establishment of epithelial cell lines from primary human explants using serum-free medium. In Vitro Cell Dev Biol Anim. 1996;32(1):29–35. doi:10.1007/BF02723028
  5. Esch EW, Bahinski A, Huh D. Organs-on-chips at the frontiers of drug discovery. Nat Rev Drug Discov. 2015;14(4):248–260. doi:10.1038/nrd4539
  6. Langford RM, et al. Mycoplasma contamination in cell culture: prevention strategies and detection. Cytotechnology. 2018;70(1):27–34. doi:10.1007/s10616-017-0128-6
  7. Maoz BM, et al. A linked organ-on-chip model of the human neurovascular unit reveals the metabolic coupling of endothelial and neuronal cells. Nat Biotechnol. 2018;36(9):865–877. doi:10.1038/nbt.4226
  8. Nawroth JC, et al. Breathing microfluidic organ-on-a-chip. Sci Adv. 2020;6(30):eaaw7505. doi:10.1126/sciadv.aaw7505
  9. Williamson A, et al. The future of the patient-specific body-on-a-chip. Lab Chip. 2013;13(18):3471–3480. doi:10.1039/c3lc50237f
  10. Kaur G, Dufour JM. Cell lines: valuable tools or useless artifacts. Spermatogenesis. 2012;2(1):1–5. doi:10.4161/spmg.19885

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