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

Product#: DCP-LL15H-QP1X
$49.50
DCP-LL15H-QP1X
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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 L-Glutamine, Sodium Pyruvate: 1X Liquid

Contains Phenol Red Contains 25mM HEPES Contains Calcium Contains Magnesium Without L-Glutamine 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). Formulated with D-galactose in place of glucose and 25 mM HEPES for CO₂-independent culture, without added L-glutamine or sodium pyruvate. Manufactured under ISO 13485:2016 using Ultrapure Type 1 water (18.2 MΩ·cm).

  • Quadruple-stage filtration to a 0.04 µm final pore size (0.1 µm ×2 + 0.04 µm ×2) for microchannel-safe purity
  • 0.9 g/L D-galactose substituted for glucose — the classical Leibovitz's L-15 design for slower glycolytic acid production under CO₂-independent conditions
  • 25 mM HEPES buffering with no added sodium bicarbonate — CO₂ incubator not required
  • L-glutamine and sodium pyruvate withheld so you can define your own metabolic supplementation strategy
  • Endotoxin release specification: < 0.05 EU/mL (LAL, USP <85>)
  • Prepared with Ultrapure Type 1 water (18.2 MΩ·cm) under an ISO 13485:2016 quality management system
  • Micro-batch production with final QC at Diagnocine, Totowa, NJ
  • Custom pH, HEPES, salts & nutrient adjustments available — support@diagnocine.com
DCP-LL15H-QP1X · Cell Culture Media UNSPSC: 41116155 | Commodity: Molecular biology and cell culture growth media | (UNv260801)
Leibovitz's L-15 Medium with 25mM HEPES w/o L-Glutamine, Sodium Pyruvate: 1X Liquid
  • GalactosePresent (0.9 g/L)
  • L-GlutamineRemoved ([-])
  • Sodium PyruvateRemoved ([-])
  • 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, away from bright 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.

filter_alt

Microchannel-safe purity

A validated 0.04 µm final filter stage helps ensure unobstructed flow through narrow microfluidic channels, reducing the sub-micron particulate load that 0.22 µm filtration leaves behind.

target

Total metabolic control

D-galactose replaces glucose to slow glycolytic acid production, while L-glutamine and sodium pyruvate are withheld so metabolic tracing and glycolysis studies proceed without background noise from these standard carbon and nitrogen sources.

water_drop

Ultrapure-grade water

Prepared with Ultrapure Type 1 water (18.2 MΩ·cm) with tight trace-metal and organic-carbon control, supporting reproducible baselines for sensitive downstream assays.

visibility

Low background for imaging

A low particulate baseline supports confocal live-cell imaging and biosensor readouts. This formulation contains phenol red and riboflavin, so optical background contribution from these components should be assessed for fluorescence- or absorbance-based assays.

science

Rich, stable nutrient profile

The complete amino acid and vitamin profile of the classical Leibovitz's L-15 formulation is produced under micro-batch precision for tight lot-to-lot consistency across long-duration MPS perfusion.

tune

Customization on demand

pH, glucose/galactose ratio, HEPES, salts, and nutrients adjusted on request. Contact support@diagnocine.com.

Purity Architecture

Quadruple-stage filtration system

This 1X liquid medium undergoes a validated four-stage sequential filtration process reaching a final pore size of 0.04 µm — a paired prefilter and final-filter architecture, run twice in series, that goes well beyond conventional 0.22 µm filtration.

  1. 1

    0.1 µm Prefiltration I

    Removes large particulates, cell debris, and protein aggregates. Protects the first 0.04 µm final filter cartridge and preserves microchannel chip geometries.

  2. 2

    0.04 µm Final filtration I

    First 0.04 µm pass; retains fine particulates and sub-micron material well below the mycoplasma size range (0.2–0.3 µm) that standard 0.22 µm media does not address.

  3. 3

    0.1 µm Prefiltration II

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

  4. 4

    0.04 µm Final filtration II — Polish

    Ultimate polishing filter ahead of aseptic fill & finish.

Performance vs. conventional media

FluxMPS™ delivers approximately 5× fewer particles ≥10 µm compared to standard 0.22 µm filtered media — a meaningful difference for long-duration perfusion in narrow microfluidic geometries.

Fewer particles ≥10 µm vs 0.22 µm media
0.04
µm final filter — sub-mycoplasma polishing
Sterility & Mycoplasma: 14-day USP <71> sterility tested per lot. Mycoplasma control is achieved through the 0.04 µm final filtration stage — a mycoplasma-retentive pore size relative to the 0.2–0.3 µm diameter of known mycoplasma species — and is not independently 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™ Leibovitz's L-15 Medium with 25mM HEPES w/o L-Glutamine, Sodium Pyruvate: 1X Liquid (DCP-LL15H-QP1X) ? Quadruple-stage filtration system (0.1 μm x2 + 0.04 μm x2) for organ-on-a-chip and microfluidic MPS 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) → aseptic fill & finish.
© Diagnocine® — DCP-LL15H-QP1X
Applications

Optimized for next-generation cell biology platforms

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

Automated Bioreactors & Robotics

Next-Generation System Uptime

An optional 0.01 µm (10 nm) ultra nano-filtered MPS Grade variant of this formulation is available for automated bioreactor and liquid-handling robotics platforms where valve and sensor protection is paramount.

  • Total particulate exclusion beyond the 0.04 µm Microfluidics Suitable tier
  • Valve & sensor protection for automated perfusion systems
  • Extended perfusion stability for long-duration, unattended runs

Inquiry Required: The 0.01 µm MPS Grade variant is produced to order. Contact support@diagnocine.com to request this grade for your platform.

Microfluidics

Micro Physiological System (MPS) & Chip

Ultra-low particulate, filtration-controlled media for perfusion in organ chips, tissue chips (ToC), and body-on-a-chip (BoC) devices.

OoCToCBoCLoCMPS
Cancer Biology

Warburg Effect & Metabolic Research

Galactose-based, glucose-free formulation supports Warburg-effect studies, forced oxidative metabolism assays, and aerobic glycolysis research.

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

iPSC-Derived Models

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

iPSC-NeuronsiPSC-CMiPSC-Hep
Vascular Biology

Endothelial & Primary Cells

Particle-controlled, CO₂-independent perfusion medium for TEER measurement, endothelial monolayer integrity, and primary cell culture outside a CO₂ incubator.

HUVECsHAECsPrimary hepatocytes
Metabolomics

Metabolic Flux Analysis

Chemically defined, glutamine- and pyruvate-free base for ¹³C metabolic tracing and NMR metabolomics. Not compatible with Agilent Seahorse XF assays, which require bicarbonate-free, phenol red-free medium — this formulation contains phenol red.

¹³C tracingNMR
Live-Cell Imaging

Microscopy & Optical Sensing

Low particulate baseline for confocal microscopy and biosensor readouts on chip; account for phenol red absorbance in fluorescence assay design.

ConfocalBiosensorsTEER
Technical Specifications

Full technical specification

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

Physical & Chemical Parameters
Parameter Specification
Formulation [+] 0.9 g/L D-Galactose, 25mM HEPES, Phenol Red / [-] L-Glutamine, Sodium Pyruvate
Appearance Clear, red-pink solution (phenol red indicator)
pH USP <791> 7.4
Osmolality USP <785> 300 - 340 mOsm/kg
Glucose Not present (0.9 g/L D-galactose substituted)
L-Glutamine Not added ([-])
Sodium Pyruvate Not added ([-])
Phenol Red 11.000 mg/L
Sterility, Purity & Safety
Parameter Specification
Endotoxin USP <85> < 0.05 EU/mL (batch release; see § Manufacturing & Compliance)
Sterility USP <71> No growth after 14 days
Mycoplasma 0.04 µm mycoplasma-retentive filtration (not tested per lot)
Water purity Ultrapure Type 1, 18.2 MΩ·cm
Manufacturing ISO 13485:2016 ISO
Fill environment ISO Class 5 (Class 100)
Storage & Logistics
Parameter Specification
Storage 2-8°C, away from bright 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)
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 21 CFR Part 820 (QMSR) aligned
Production 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: 34 components across 4 categories. All values are per-lot verified and reported on the Certificate of Analysis (CoA).

INORGANIC SALTS
Component CAS Number mg/L
INORGANIC SALTS
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
AMINO ACIDS
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-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
i-Inositol 87-89-8 2.000
OTHERS
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, glucose/galactose ratio, 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.

water_drop

Ultrapure Type 1 Water

18.2 MΩ·cm with tight trace-metal and organic-carbon control, prepared to minimize contribution to assay background.

biotech

ISO Class 5 Fill & Finish

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

assignment

Micro-Batch Precision

Small-batch production targeting tight osmolality (±5 mOsm/kg) and pH (±0.05) process control — supporting reproducible long-duration MPS experiments.

Endotoxin — USP <85> BET

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

Filtration Validation

Quadruple-stage 0.1 µm / 0.04 µm filtration train (0.1 µm ×2 + 0.04 µm ×2) validated per manufacturing batch.

Osmolality — USP <785>

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

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.
CoA Request: Available at no charge for any production lot of FluxMPS™ Leibovitz's L-15 Medium with 25mM HEPES w/o L-Glutamine, Sodium Pyruvate: 1X Liquid (DCP-LL15H-QP1X). Email support@diagnocine.com.
Product Comparison

How DCP-LL15H-QP1X compares

Differences in grade, filtration, mycoplasma barrier, and endotoxin release specification versus conventional L-15 media.

Parameter DCP-LL15H-QP1X (FluxMPS™) Standard L-15 (0.22 µm) Competitor L-15 (0.22 µm)
Grade Microfluidics Suitable Not specified Not specified
Formulation definition [+] 0.9 g/L Galactose, 25mM HEPES / [-] L-Glutamine, 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> Method 1 compliance check_circle cancel cancel
Water quality Ultrapure Type 1, 18.2 MΩ·cm Unspecified Unspecified
Manufacturing QMS ISO 13485:2016 Varies Varies
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 L-Glutamine, Sodium Pyruvate: 1X Liquid (DCP-LL15H-QP1X).

Yes. DCP-LL15H-QP1X is Microfluidics Suitable and engineered for OoC, MPS, and microfluidic applications. The 0.04 µm final filtration stage helps reduce mycoplasma-scale material and sub-micron particulates that can cause microchannel clogging in standard 0.22 µm media.
Four sequential stages (0.1 µm ×2 + 0.04 µm ×2) reduce material in the mycoplasma size range (0.2–0.3 µm) and sub-visible particulates entirely missed by conventional 0.22 µm filters — resulting in approximately 5× fewer particles by USP <788> Method 1 (light obscuration).
L-glutamine and sodium pyruvate are withheld so you can define your own metabolic supplementation for glycolysis, glutaminolysis, or metabolic tracing studies. D-galactose (0.9 g/L) is already present as the carbon source, per the classical Leibovitz's L-15 design. Add L-glutamine or a stable dipeptide substitute, and sodium pyruvate, at the concentrations appropriate for your cell line. Contact support@diagnocine.com for custom pre-supplementation.
No. This formulation contains no sodium bicarbonate and is buffered with 25 mM HEPES, making it suitable for CO₂-independent incubation — consistent with the classical Leibovitz's L-15 design.
Yes. DCP-LL15H-QP1X is a basal medium compatible with FBS (2–10%), human serum, GlutaMAX, EGF, FGF, VEGF, and antibiotics. Pre-filter serum and protein-containing additions through a 0.2 µm low-protein-binding PES or PVDF filter before combining; defined, protein-free additions may use 0.1 µm. Do not use a 0.04 µm filter for supplements — it retains serum proteins and lipoproteins.
Endotoxin is controlled per manufacturing batch. 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. Lot-specific results are available on the Certificate of Analysis — request at support@diagnocine.com.
Yes — a full CoA per lot includes: lot number, expiry (12 months from date of manufacture, unopened), appearance, pH (USP <791>), osmolality (USP <785>), endotoxin (USP <85>), sterility (USP <71>), filtration validation, particulate compliance (USP <788>), 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.a120327
  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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