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

Product#: DCP-LL15-R1X
$55.00
DCP-LL15-R1X
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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 Phenol Red: 1X Liquid

Contains L-Glutamine Contains 25mM HEPES Contains Calcium Contains Magnesium Contains Sodium Pyruvate Without Phenol Red

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). This CO₂-independent, HEPES-buffered, phenol-red-free formulation uses D-galactose (900 mg/L) rather than glucose as its carbon source and is manufactured under ISO 13485:2016 in an ISO Class 5 fill environment.

  • CO₂-independent Leibovitz's L-15 base with 25 mM HEPES buffering — no sodium bicarbonate, suitable for ambient-air incubation
  • D-Galactose-based carbon source (900 mg/L) in place of glucose, supporting metabolic and Warburg-effect study designs
  • L-Glutamine (300 mg/L) and Sodium Pyruvate (550 mg/L) included as ready-to-use energy substrates
  • Phenol-red-free formulation — pale/colorless clear solution suited to optical and fluorescence-based assays
  • Quadruple-stage filtration train (0.1 µm → 0.04 µm → 0.1 µm → 0.04 µm) with a 0.04 µm final polish
  • Endotoxin release specification < 0.05 EU/mL (LAL, USP <85>), tested per manufacturing batch
  • Manufactured under an ISO 13485:2016 quality management system; final QC and packaging at Diagnocine, Totowa, NJ, USA
  • Custom pH, HEPES, salts, and nutrient composition available on request — support@diagnocine.com
DCP-LL15-R1X · Cell Culture Media UNSPSC: 41116155 | Commodity: Molecular biology and cell culture growth media | (UNv260801)
Leibovitz's L-15 Medium with 25mM HEPES w/o Phenol Red: 1X Liquid
  • Carbon SourceD-Galactose, 900 mg/L (no glucose)
  • L-Glutamine300 mg/L ([+])
  • Sodium Pyruvate550 mg/L ([+])
  • 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 organisms in the mycoplasma size range (0.2–0.3 µm), sub-visible particulates, and microaggregates to pass freely — clogging microchannels, corrupting biosensors, and confounding metabolic assays. FluxMPS™ closes that gap.

filter_alt

Microchannel-safe purity

A 0.04 µm final filter, tested to USP <788> Method 1 (light obscuration), supports unobstructed flow in channels as narrow as 50 µm.

target

Total metabolic control

A precisely defined galactose/pyruvate carbon source enables Warburg-effect studies,[3] glycolysis inhibition, and ¹³C metabolic tracing.

water_drop

Ultrapure-grade water

Prepared with Ultrapure Type 1 water (18.2 MΩ·cm) — formulated for low trace-metal and organic-carbon content, supporting consistent lot-to-lot formulation.

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

A validated four-stage sequential filtration train reaching a final pore size of 0.04 µm — two paired prefilter/final-filter passes run in series, each 0.04 µm cartridge protected by its own dedicated 0.1 µm prefilter.

  1. 1

    0.1 µm Prefiltration I

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

  2. 2

    0.04 µm Final filtration I

    First 0.04 µm pass; retains sub-micron particulates and microaggregates that a 0.22 µm filter does not.

  3. 3

    0.1 µm Prefiltration II

    Second, independent prefilter dedicated to protecting the second 0.04 µm cartridge, giving the train full redundancy.

  4. 4

    0.04 µm Final filtration II — Polish

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

Purity architecture, in practice

The quadruple-stage train — two prefilter/final-filter pairs in series — extends particulate and bioburden control well beyond single-pass 0.22 µm filtration, supporting long-duration perfusion in narrow microfluidic channels.

4
Sequential filtration passes
0.04
µm final filter — sub-mycoplasma polishing
Sterility & mycoplasma control: 14-day USP <71> sterility tested per batch. Mycoplasma control is achieved through 0.1 µm mycoplasma-retentive filtration (not tested per lot); organisms in the mycoplasma size range (0.2–0.3 µm) are well above the 0.04 µm final cut-off.[9]
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 Phenol Red 1X Liquid (DCP-LL15-R1X) ? Quadruple-stage filtration system (0.1 μm ×2 + 0.04 μm ×2) 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) → ISO Class 5 aseptic fill.
© Diagnocine® — DCP-LL15-R1X
Applications

Optimized for next-generation cell biology platforms

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

Automated Bioreactors & Robotics

Next-Generation System Uptime

For continuous, unattended perfusion systems, Diagnocine offers an optional 0.01 µm (10 nm) ultra nano-filtered MPS Grade variant of this formulation, engineered for automated bioreactors and robotic liquid-handling platforms.

  • Total particulate exclusion beyond the 0.04 µm Microfluidics Suitable tier
  • Valve and sensor protection in automated dosing systems
  • Extended perfusion stability for multi-week unattended runs

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

Microfluidics

Micro Physiological System (MPS) & Chip

Ultra-low particulate, HEPES-buffered, CO₂-independent medium for perfusion in organ chips, tissue chips (ToC), and body-on-a-chip (BoC) devices.

OoCToCBoCMPS
Cancer Biology

Warburg Effect & Metabolic Research

Galactose-based, glucose-free carbon source enables Warburg-effect studies, aerobic glycolysis suppression, 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 perfusion media for TEER measurement, endothelial monolayer integrity, and primary cell culture.

HUVECsHAECsPrimary hepatocytes
Metabolomics

Metabolic Flux Analysis

Bicarbonate-free, phenol-red-free formulation compatible with ¹³C metabolic tracing, Agilent Seahorse XF respiratory assays, and NMR metabolomics.

¹³C tracingSeahorse XFNMR
Live-Cell Imaging

Microscopy & Optical Sensing

Ultra-low particulate baseline supports confocal microscopy, fluorescent biosensors, and automated imaging on chip.

ConfocalBiosensorsTEER
Technical Specifications

Full technical specification

Every batch of FluxMPS™ Leibovitz's L-15 Medium with 25mM HEPES w/o Phenol Red: 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, 25mM HEPES, Calcium, Magnesium, Sodium Pyruvate / [-] Phenol Red
Carbon Source D-Galactose, 900 mg/L (no glucose)
Appearance Clear solution, pale/colorless (phenol-red-free)
pH USP <791> 7.4
Osmolality USP <785> 300 - 340 mOsm/kg H2O
L-Glutamine 300 mg/L ([+])
Sodium Pyruvate 550 mg/L ([+])
Phenol Red Not added ([-])
Sterility, Purity & Safety Parameters
Parameter Specification
Endotoxin USP <85> BET < 0.05 EU/mL (batch release; see Manufacturing & Compliance)
Sterility USP <71> No growth after 14 days
Mycoplasma 0.1 µm mycoplasma-retentive filtration (not tested per lot)
Particulate USP <788> Method 1 Light-obscuration particle count compliant
Water purity Ultrapure Type 1, 18.2 MΩ·cm
Manufacturing ISO 13485:2016 ISO
Fill environment ISO Class 5 (Class 100)
Grade Microfluidics Suitable (0.04 µm cut-off)
Storage, Handling & Logistics
Parameter Specification
Storage temperature 2-8°C, protect from light
Freeze–thaw Do not freeze
Shelf life 12 months from date of manufacture, unopened
Shipping condition Cold pack (2–8°C)
CO₂ requirement Not required — HEPES-buffered, CO₂-independent formulation (no sodium bicarbonate)
Raw Materials & Regulatory Traceability
Parameter Specification
Raw material grade Research-grade, per-lot CoA traceable
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 Research Use Only (RUO)
Formulation

Full composition (mg/L)

Every ingredient below is present in this 1X liquid formulation at the exact concentration listed. Total: 35 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-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
Sodium pyruvate 113-24-6 550.000
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 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 resistivity with low trace-metal and organic-carbon (TOC) content, supporting consistent formulation across lots.

biotech

ISO Class 5 Fill & Finish

Validated ISO Class 5 laminar-flow workstation with real-time particle monitoring, preserving filtration gains through final fill.

assignment

Micro-Batch Precision

Small-batch production for tight lot-to-lot consistency across pH, osmolality, and endotoxin — critical for reproducible long-duration MPS experiments.

Endotoxin — USP <85> BET

LAL assay; assay sensitivity 0.005 EU/mL. Release specification: < 0.05 EU/mL, tested per manufacturing batch.

Particulate — USP <788> Method 1

Light-obscuration particle count testing confirms compliance with subvisible particulate limits, supporting clean microchannel flow.

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 at support@diagnocine.com.
Product Comparison

How DCP-LL15-R1X compares

Key differences in grade, filtration, mycoplasma control, and endotoxin specification versus conventional 0.22 µm filtered L-15 media.

Parameter DCP-LL15-R1X (FluxMPS™) Standard L-15 (0.22 µm) Competitor L-15 (0.22 µm)
Grade Microfluidics Suitable Not applicable Not applicable
Formulation definition [+] L-Glutamine, 25mM HEPES, Calcium, Magnesium, Sodium Pyruvate / [-] Phenol Red Standard Standard
Final filtration pore size 0.04 µm (40 nm) 0.22 µm 0.22 µm
Number of filtration stages 4 (Quadruple: 0.1×2 + 0.04×2) 1 1
Mycoplasma-retentive 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 (Method 1) 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 Phenol Red: 1X Liquid (DCP-LL15-R1X).

Yes. DCP-LL15-R1X is engineered for OoC, microfluidic, and MPS applications. Its 0.04 µm final filtration stage retains particulates and organisms in the mycoplasma size range (0.2–0.3 µm) that pass through standard 0.22 µm filters, reducing the risk of microchannel clogging.
Four sequential stages (0.1 µm ×2 + 0.04 µm ×2) target particulates and organisms in the mycoplasma size range (0.2–0.3 µm) that conventional 0.22 µm filters do not retain, verified per USP <788> Method 1 (light obscuration) particulate testing.
Leibovitz's L-15 base medium is formulated with D-galactose (900 mg/L) and sodium pyruvate (550 mg/L) rather than glucose, supporting CO₂-independent metabolism and Warburg-effect study designs. This formulation already contains L-Glutamine (300 mg/L) and 25 mM HEPES; no additional glutamine or buffer is required. Contact support@diagnocine.com for custom carbon-source formulations.
No. This formulation is HEPES-buffered (25 mM) and contains no sodium bicarbonate. It is formulated for CO₂-independent culture and can be used in ambient air.
Yes. DCP-LL15-R1X is a basal medium compatible with FBS (2–10%), human serum, EGF, FGF, VEGF, and antibiotics. Pre-filter serum-containing additions through a 0.2 µm low-protein-binding PES or PVDF filter before combining; protein-free, defined additions may use 0.1 µm filtration.
Every batch is tested before release 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. A Certificate of Analysis with the lot-specific result is available on request at support@diagnocine.com.
Yes — a full CoA per lot includes: 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. 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. Vander Heiden MG, et al. Understanding the Warburg effect. Science. 2009;324:1029–1033. doi:10.1126/science.1160809
  4. 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
  5. van Duinen V, et al. Microfluidic 3D cell culture. Curr Opin Biotechnol. 2015;35:118–126. doi:10.1016/j.copbio.2015.05.002
  6. Jang KJ, et al. Reproducing human drug toxicities using a Liver-Chip. Sci Transl Med. 2019;11:eaax5516. doi:10.1126/scitranslmed.aax5516
  7. Kasendra M, et al. Primary human Small Intestine-on-a-Chip. Sci Rep. 2018;8:2871. doi:10.1038/s41598-018-21201-7
  8. Skardal A, et al. Multi-tissue organ-on-a-chip platform. Sci Rep. 2017;7:8837. doi:10.1038/s41598-017-08879-x
  9. Rottem S. Interaction of mycoplasmas with host cells. Physiol Rev. 2003;83:417–432. doi:10.1152/physrev.00030.2002

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