FluxMPS™ Leibovitz's L-15 Medium with 25mM HEPES w/o Sodium Pyruvate: 1X Liquid

Product#: DCP-LL15H-P1X
$49.50
DCP-LL15H-P1X
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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™ Leibovitz's L-15 Medium with 25mM HEPES w/o Sodium Pyruvate: 1X Liquid

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

Microfluidics Suitable, quadruple-stage ultra-filtered (0.1 µm ×2 + 0.04 µm ×2) 1X liquid Leibovitz's L-15 medium engineered for microfluidic channels, organ-on-a-chip (OoC), and microphysiological systems (MPS). Buffered with 25 mM HEPES and formulated without sodium pyruvate, this bicarbonate-free, CO₂-independent medium is manufactured under an ISO 13485:2016 quality system using a validated four-stage 0.1 µm/0.04 µm filtration train.

  • Leibovitz's L-15 formulation buffered with 25 mM HEPES; bicarbonate-free and CO₂-independent, suited to open-bench and microfluidic culture
  • 0.9 g/L D-Galactose provided as the carbon source in place of glucose, consistent with the classical L-15 design for ambient-air culture
  • L-Glutamine included at 300 mg/L ([+]); sodium pyruvate not added ([-]) for defined metabolic control
  • Quadruple-stage filtration train (0.1 µm → 0.04 µm → 0.1 µm → 0.04 µm) validated for microfluidic channel compatibility
  • Endotoxin release specification: < 0.05 EU/mL (USP <85> BET), controlled per manufacturing batch
  • Manufactured under an ISO 13485:2016 quality management system; final QC and packaging at Diagnocine, Totowa, NJ
  • Custom pH, HEPES, salts, and nutrient adjustments available on request — support@diagnocine.com
DCP-LL15H-P1X · Cell Culture Media UNSPSC: 41116155 | Commodity: Molecular biology and cell culture growth media | (UNv260801)
Leibovitz's L-15 Medium with 25mM HEPES w/o Sodium Pyruvate: 1X Liquid
  • Galactose0.9 g/L (Present)
  • L-Glutamine300 mg/L ([+])
  • Sodium PyruvateNot added ([-])
  • pH (USP <791>)7.4
  • Osmolality (USP <785>)300 - 340 mOsm/kg
  • Endotoxin (USP <85>)< 0.05 EU/mL
  • Filtration0.1µm ×2 + 0.04µm ×2
  • Storage2-8°C, protect from light
  • Shelf Life12 months from date of manufacture, unopened
  • ShippingCold pack (2–8°C)
ISO 13485:2016 USP <85> <785> <788> RUO
Why FluxMPS™

Engineered where standard media fails

Conventional 0.22 µm filtered media allows mycoplasma (0.2–0.3 µm), sub-visible particulates, and microaggregates to pass freely — clogging microchannels, corrupting biosensors, and invalidating metabolic assays. FluxMPS™ closes that gap with a validated 0.04 µm final polish.

filter_alt

Microchannel-safe purity

A 0.04 µm final filter provides a substantially finer cut-off than conventional single-stage 0.22 µm filtration, supporting more consistent flow through narrow microfluidic geometries.

target

Total metabolic control

Galactose in place of glucose enables defined-carbon-source studies, Warburg-effect research, and ¹³C metabolic tracing on a precisely specified baseline.

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Ultrapure-grade water

Prepared with Ultrapure Type 1 water (18.2 MΩ·cm) with tight trace-metal and organic-carbon control, supporting sensitive biosensor and electrochemical chip applications.

visibility

Low background for imaging

Ultra-low particulate baseline supports confocal live-cell imaging, fluorescent biosensors, and automated high-content analysis on chip.

science

Rich, stable nutrient profile

4× BME amino acid and vitamin concentrations with micro-batch precision — tight lot-to-lot consistency for long-duration MPS perfusion.

tune

Customization on demand

pH, HEPES, salts, and nutrients adjusted on request. Contact support@diagnocine.com.

Purity Architecture

Quadruple-stage filtration system

FluxMPS™ Leibovitz's L-15 Medium with 25mM HEPES w/o Sodium Pyruvate is manufactured with a validated four-stage sequential filtration train reaching a final pore size of 0.04 µm — two dedicated prefilter/final-filter pairs run in series for redundant clearance.

  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

    Retains sub-micron particulates and microaggregates that pass through 0.22 µm filtration unimpeded.

  3. 3

    0.1 µm Prefiltration II

    A second dedicated prefilter, protecting the second 0.04 µm final filter cartridge for redundant clearance.

  4. 4

    0.04 µm Final filtration II — Polish

    Ultimate polishing filter; aseptic fill in a validated ISO Class 5 (Class 100) laminar-flow workstation.

Filtration architecture

Two dedicated 0.1 µm/0.04 µm prefilter and final-filter pairs run in series, each 0.04 µm final filter protected by its own 0.1 µm prefilter, for a validated final cut-off well below conventional 0.22 µm filtration.

4
Sequential filtration passes (0.1 µm ×2 + 0.04 µm ×2)
0.04
µm Final filter — sub-mycoplasma polishing
Sterility & Mycoplasma: 14-day USP <71> sterility tested per lot. Mycoplasma control is by 0.1 µm mycoplasma-retentive filtration (not tested per lot). Known mycoplasma are typically 0.2–0.3 µm in diameter, above the 0.1 µm retentive cut-off.
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™ Leibovitz's L-15 Medium with 25mM HEPES w/o Sodium Pyruvate: 1X Liquid (DCP-LL15H-P1X) ? Quadruple-stage filtration system (0.1 μm x2 + 0.04 μm x2) for organ-on-a-chip and microfluidic cell culture | Diagnocine
Figure 1. FluxMPS™ Quadruple-stage filtration: 0.1µm Prefiltration I → 0.04µm Final filtration I → 0.1µm Prefiltration II → 0.04µm Final filtration II (Polish) → ISO Class 5 aseptic fill.
© Diagnocine® — DCP-LL15H-P1X
Applications

Optimized for next-generation cell biology platforms

FluxMPS™ Leibovitz's L-15 Medium with 25mM HEPES w/o Sodium Pyruvate: 1X Liquid is validated for applications where microchannel cleanliness, signal fidelity, and CO₂-independent culture stability are critical.

Automated Bioreactors & Robotics

Next-Generation System Uptime

For automated bioreactor and robotic liquid-handling platforms requiring the finest available cut-off, an optional 0.01 µm (10 nm) ultra nano-filtered MPS Grade variant of this formulation is available on request.

  • Total Particulate Exclusion — six-stage cascade down to 0.01 µm
  • Valve & Sensor Protection — reduced risk of micro-valve and sensor fouling in closed-loop systems
  • Extended Perfusion Stability — supports longer unattended perfusion intervals

Inquiry Required: The 0.01 µm MPS Grade variant is produced to order. Contact support@diagnocine.com for lead time and pricing.

Microfluidics

Micro Physiological System (MPS) & Chip

Ultra-low particulate media for perfusion in organ chips, tissue chips (ToC), and body-on-a-chip (BoC) devices, in an ambient-air, CO₂-independent format.

OoCToCBoCMPS
Cancer Biology

Warburg Effect & Metabolic Research

Galactose-based carbon source formulation supports Warburg-effect studies, aerobic glycolysis research, and cancer metabolomics.

MCF-7MDA-MB-231HeLaA549
Stem Cell Biology

iPSC-Derived Models

Ultra-clean, low-endotoxin baseline minimizes non-specific signals in iPSC differentiation and functional organoid readouts.

iPSC-NeuronsiPSC-CMiPSC-Hep
Vascular Biology

Endothelial & Primary Cells

Particle-free, CO₂-independent perfusion media for TEER measurement, endothelial monolayer integrity, and primary cell culture on the open bench.

HUVECsHAECsPrimary hepatocytes
Metabolomics

Metabolic Flux Analysis

Chemically defined, galactose-based formulation for ¹³C metabolic tracing and NMR metabolomics. Not compatible with Agilent Seahorse XF assays, which require bicarbonate-free, phenol-red-free medium.

¹³C tracingNMR
Live-Cell Imaging

Microscopy & Optical Sensing

Low particulate baseline for confocal microscopy, fluorescent biosensors, and automated imaging on chip.

ConfocalBiosensorsTEER
Technical Specifications

Full technical specification

Every lot of FluxMPS™ Leibovitz's L-15 Medium with 25mM HEPES w/o Sodium Pyruvate: 1X Liquid is released against comprehensive multi-parameter QC specifications. Available pack sizes: 500 mL, 1000 mL.

Physical & Chemical Parameters
Parameter Specification
Formulation [+] L-Glutamine, Phenol Red, HEPES, Calcium, Magnesium / [-] Sodium Pyruvate
Appearance Red to pink-red, clear solution (phenol red pH indicator present)
pH USP <791> 7.4
Osmolality USP <785> 300 - 340 mOsm/kg H₂O
Glucose Not added; D-Galactose (0.9 g/L) provided as carbon source
L-Glutamine 300 mg/L ([+])
Sodium Pyruvate Not added ([-])
Phenol Red 11 mg/L ([+])
Sterility, Purity & Safety Parameters
Parameter Specification
Endotoxin USP <85> < 0.05 EU/mL
Sterility USP <71> No growth after 14 days
Mycoplasma 0.1 µm mycoplasma-retentive filtration (not tested per lot)
Particulate ≥10 µm <788> Method 1 Meets acceptance criteria
Particulate ≥25 µm <788> Method 1 Meets acceptance criteria
Water purity Ultrapure Type 1, 18.2 MΩ·cm
Manufacturing ISO 13485:2016 ISO
Fill environment ISO Class 5 (Class 100)
Storage, Handling & Logistics
Parameter Specification
Storage 2-8°C, protect from light
Freeze–thaw Do not freeze
Shelf life 12 months from date of manufacture, unopened
Shipping Cold pack (2–8°C)
CO₂ requirement Not required (CO₂-independent; HEPES-buffered, bicarbonate-free)
Raw Materials & Regulatory Traceability
Parameter Specification
Raw material grade Pharmaceutical/research grade CoA
Manufacturing QMS ISO 13485:2016 ISO
UNSPSC 41116155 — Molecular biology and cell culture growth media (UNv260801)
Regulatory alignment 21 CFR Part 820 (QMSR) aligned
Production method Micro-batch; Totowa, NJ, USA
Intended use RUO only
Formulation

Full composition (mg/L)

Every ingredient below is present in this 1X liquid formulation at the exact concentration listed. Total: 35 components. All values are per-lot verified and reported on the Certificate of Analysis (CoA).

INORGANIC SALTS
Component CAS Number mg/L
Calcium chloride dihydrate 10035-04-8 185.000
Magnesium chloride hexahydrate 7791-18-6 200.000
Magnesium sulfate anhydrous 7487-88-9 97.720
Potassium chloride 7447-40-7 400.000
Potassium phosphate monobasic 7778-77-0 60.000
Sodium chloride 7647-14-5 8000.000
Sodium dihydrogen phosphate anhydrous 7558-80-7 190.120
AMINO ACIDS
Component CAS Number mg/L
L-Alanine 56-41-7 225.000
Glycine 56-40-6 200.000
L-Arginine (free base) 74-79-3 500.000
L-Asparagine 70-47-3 250.000
L-Cysteine (free base) 52-90-4 120.000
L-Glutamine 56-85-9 300.000
L-Histidine (free base) 71-00-1 250.000
L-Isoleucine 73-32-5 250.000
L-Leucine 61-90-5 125.000
L-Lysine hydrochloride 657-27-2 94.000
L-Methionine 63-68-3 75.000
L-Phenylalanine 63-91-2 125.000
L-Serine 56-45-1 200.000
L-Threonine 72-19-5 300.000
L-Tryptophan 73-22-3 20.000
L-Tyrosine disodium salt   276.160
L-Valine 72-18-4 100.000
Component CAS Number mg/L
VITAMINS
Choline chloride 67-48-1 1.000
D-Ca-Pantothenate 137-08-6 1.000
Folic acid 59-30-3 1.000
Nicotinamide 98-92-0 1.000
Pyridoxine hydrochloride 58-56-0 1.000
Riboflavin-5-phosphate sodium salt 130-40-5 0.100
Thiamine hydrochloride 67-03-8 1.000
OTHERS
i-Inositol 87-89-8 2.000
D-Galactose 59-23-4 900.000
HEPES buffer 7365-45-9 5958.000
Phenol red sodium salt 34487-61-1 11.000
Custom formulations: pH, HEPES, salts, and individual nutrient levels adjustable on request. Contact support@diagnocine.com.
Quality Assurance

Manufacturing & compliance

Every batch is subjected to multi-parameter lot-release testing before distribution.

verified

ISO 13485:2016 QMS

Manufactured by ISO 13485-certified suppliers. Final packaging, QA and testing at DiagnoCine R&D Center; customization at DiagnoCine Precision, Totowa, NJ, USA.

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Ultrapure Type 1 Water

18.2 MΩ·cm, low trace-metal and organic-carbon content, USP <85> endotoxin-tested.

biotech

ISO Class 5 Fill & Finish

Validated ISO Class 5 laminar-flow workstation with real-time particle monitoring. Preserves all filtration gains in the final container.

assignment

Micro-Batch Precision

Small-batch production with tight lot-to-lot consistency — important for reproducible long-duration MPS experiments.

Endotoxin — USP <85> BET

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

Particulate — USP <788> Method 1

Light-obscuration particle count test. Each lot meets Method 1 acceptance criteria.

Osmolality — USP <785>

Freezing-point depression osmometry. Release range: 300 - 340 mOsm/kg H₂O.

Certificate of Analysis (CoA)

Full CoA per lot. Request at support@diagnocine.com with lot number.

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. Email support@diagnocine.com.
Product Comparison

How DCP-LL15H-P1X compares

Filtration architecture, mycoplasma-barrier design, water quality, and QC depth relative to conventionally filtered L-15 media.

Parameter DCP-LL15H-P1X (FluxMPS™) Standard L-15 (0.22 µm) Competitor L-15 (0.22 µm)
Grade Microfluidics Suitable Not specified Not specified
Formulation definition [+] L-Glutamine, Phenol Red, HEPES, Calcium, Magnesium / [-] Sodium Pyruvate Standard Standard
Final filtration pore size 0.04 µm (40 nm) 0.22 µm 0.22 µm
Filtration stages 4 (Quadruple) 1 1
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 <788> particulate compliance check_circle Method 1 cancel cancel
Water quality Ultrapure Type 1, 18.2 MΩ·cm Not specified Not specified
Manufacturing QMS ISO 13485:2016 Not specified Not specified
Microfluidic channel compatibility check_circle cancel cancel
Custom formulation check_circle On request cancel cancel

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™ Leibovitz's L-15 Medium with 25mM HEPES w/o Sodium Pyruvate: 1X Liquid (DCP-LL15H-P1X).

Yes. DCP-LL15H-P1X is manufactured for organ-on-a-chip, microfluidic, and MPS applications. The 0.04 µm final filter and 0.1 µm mycoplasma-retentive prefilter reduce sub-micron particulates that can contribute to microchannel clogging in standard 0.22 µm media.
Four sequential stages (0.1 µm → 0.04 µm → 0.1 µm → 0.04 µm) capture particulates and organisms that a single-stage 0.22 µm filter cannot, including mycoplasma (typically 0.2–0.3 µm in diameter), assessed by USP <788> Method 1 (light obscuration).
This formulation uses D-Galactose (0.9 g/L) as its designed carbon source, consistent with the classical Leibovitz's L-15 formula for CO₂-independent culture, and does not include sodium pyruvate. If your protocol requires sodium pyruvate, it can be added at time of use, or a custom formulation with pyruvate included can be produced — contact support@diagnocine.com.
No. This formulation does not contain sodium bicarbonate and is buffered with 25 mM HEPES, making it suitable for CO₂-independent, ambient-air incubation — the standard use case for Leibovitz's L-15 medium.
Yes. This basal medium is compatible with FBS (typically 2–10%), human serum, growth factors (e.g., EGF, FGF, VEGF), and antibiotics added at time of use. Pre-filter serum-containing or protein-containing additions through a 0.2 µm low-protein-binding PES or PVDF membrane before combining; do not use a 0.04 µm membrane for these additions, as it will retain serum proteins and lipoproteins.
Endotoxin is controlled per manufacturing batch to a release specification of < 0.05 EU/mL, tested by LAL assay per USP <85> (assay sensitivity 0.005 EU/mL). Every batch is tested before release; the lot-specific result is reported on the Certificate of Analysis — request at support@diagnocine.com.
Yes — a full CoA is available per lot, including lot number, expiry, appearance, pH (USP <791>), osmolality (USP <785>), endotoxin (USP <85>), sterility (USP <71>), particulate count (USP <788> Method 1), and cultural response. Email support@diagnocine.com.
Scientific References

Supporting literature

  1. Leibovitz A. The growth and maintenance of tissue-cell cultures in free gas exchange with the atmosphere. Am J Hyg. 1963;78:173–180. doi:10.1093/oxfordjournals.aje.a120328
  2. Huh D, et al. Reconstituting organ-level lung functions on a chip. Science. 2010;328:1662–1668. doi:10.1126/science.1188302
  3. Bhatia SN, Ingber DE. Microfluidic organs-on-chips. Nat Biotechnol. 2014;32:760–772. doi:10.1038/nbt.2989
  4. Vander Heiden MG, et al. Understanding the Warburg effect. Science. 2009;324:1029–1033. doi:10.1126/science.1160809
  5. Sontheimer-Phelps A, et al. Modelling cancer in microfluidic human organs-on-chips. Nat Rev Cancer. 2019;19:65–81. doi:10.1038/s41568-018-0104-6
  6. van Duinen V, et al. Microfluidic 3D cell culture. Curr Opin Biotechnol. 2015;35:118–126. doi:10.1016/j.copbio.2015.05.002
  7. Jang KJ, et al. Reproducing human drug toxicities using a Liver-Chip. Sci Transl Med. 2019;11:eaax5516. doi:10.1126/scitranslmed.aax5516
  8. Kasendra M, et al. Primary human Small Intestine-on-a-Chip. Sci Rep. 2018;8:2871. doi:10.1038/s41598-018-21201-7

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