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

Product#: DCP-LL15-P1X
$44.00
DCP-LL15-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 w/o Sodium Pyruvate: 1X Liquid

Contains L-Glutamine Contains Phenol Red 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). This CO₂-independent formulation is built on D-galactose rather than glucose and does not contain sodium bicarbonate, and is manufactured under an ISO 13485:2016 quality management system with an ISO Class 5 (Class 100) aseptic fill.

  • Leibovitz's L-15 base formulated with 0.9 g/L D-galactose as the primary carbon source, replacing glucose, for CO₂-independent culture without sodium bicarbonate buffering
  • Sodium pyruvate omitted from the formulation ([-] Sodium Pyruvate) — supplement directly if your protocol requires it
  • L-Glutamine included at 300 mg/L ([+] L-Glutamine) for direct nitrogen and energy metabolism support
  • Quadruple-stage filtration train (0.1 µm ×2 + 0.04 µm ×2) reaching a validated 0.04 µm final pore size
  • 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
  • Custom pH, HEPES, salts, and nutrient adjustments available on request — support@diagnocine.com
DCP-LL15-P1X · Cell Culture Media UNSPSC: 41116155 | Commodity: Molecular biology and cell culture growth media | (UNv260801)
Leibovitz's L-15 Medium w/o Sodium Pyruvate: 1X Liquid
  • Galactose900 mg/L
  • L-Glutamine300 mg/L ([+])
  • 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, 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 (approximately 0.2–0.3 µm), sub-visible particulates, and microaggregates to pass freely — clogging microchannels, corrupting biosensors, and complicating metabolic assays. FluxMPS™ closes that gap.

filter_alt

Microchannel-safe purity

0.04 µm final filtration reduces particulate load for use in narrow microfluidic channels; particulates are monitored per USP <788> Method 1 (light obscuration).

target

Total metabolic control

A defined D-galactose carbon source and controlled amino acid profile support CO₂-independent culture, Warburg-effect studies, and glycolysis-focused metabolic research.

water_drop

Ultrapure-grade water

Prepared with Ultrapure Type 1 water (18.2 MΩ·cm) with tightly controlled trace-metal and organic carbon (TOC) content.

visibility

Low background for imaging

Ultra-low particulate baseline supports confocal live-cell imaging, fluorescent biosensors, and automated high-content analysis on chip. Note: the included phenol red indicator may contribute background fluorescence in some optical channels.

science

Rich, stable nutrient profile

A comprehensive amino acid and vitamin profile matched to the classical Leibovitz's L-15 formulation, produced under micro-batch conditions for tight lot-to-lot consistency.

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

FluxMPS™ Leibovitz's L-15 Medium w/o Sodium Pyruvate is manufactured using a validated four-stage sequential filtration train — two paired prefilter/final-filter passes — reaching a final pore size of 0.04 µm, built for microfluidic channels and microphysiological systems (MPS).

  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

    First 0.04 µm pass; retains sub-micron particulates and microaggregates that pass a conventional 0.22 µm filter.

  3. 3

    0.1 µm Prefiltration II

    Second dedicated prefilter, protecting the second 0.04 µm final filter cartridge.

  4. 4

    0.04 µm Final filtration II — Polish

    Ultimate polishing filter ahead of aseptic fill & finish.

Filtration architecture

The train runs as two dedicated prefilter/final-filter pairs in series — each 0.04 µm final filter is protected by its own 0.1 µm prefilter — rather than a single descending cascade, giving full redundancy across the four passes.

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. The 0.1 µm stages provide mycoplasma-retentive filtration (not tested per lot); the 0.04 µm final stage adds a further sub-mycoplasma margin. Mycoplasma diameter is approximately 0.2–0.3 µm.
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 w/o Sodium Pyruvate: 1X Liquid (DCP-LL15-P1X) ? Quadruple-stage filtration system (0.1 μm x2 + 0.04 μm x2) for organ-on-a-chip and microfluidic microphysiological systems (MPS) | 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-P1X
Applications

Optimized for next-generation cell biology platforms

FluxMPS™ Leibovitz's L-15 Medium w/o Sodium Pyruvate: 1X Liquid is suited to applications where microchannel cleanliness, CO₂-independent buffering, and metabolic precision are important.

Automated Bioreactors & Robotics

Next-Generation System Uptime

For automated bioreactors and robotic liquid-handling platforms, Diagnocine also offers this formulation as an optional 0.01 µm (10 nm) ultra nano-filtered MPS Grade variant — the separate six-stage tier described in the Purity Architecture note above.

  • Total Particulate Exclusion — six-stage cascade down to 0.01 µm
  • Valve & Sensor Protection — minimizes microparticle accumulation in automated fluidics
  • Extended Perfusion Stability — supports long-duration unattended runs

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

Microfluidics

Micro Physiological System (MPS) & Chip

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

OoCToCBoCMPS
Cancer Biology

Warburg Effect & Metabolic Research

A galactose-based, defined carbon source formulation for CO₂-independent Warburg-effect studies, aerobic glycolysis, 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-controlled perfusion media for TEER measurement, endothelial monolayer integrity, and primary cell culture, without CO₂ incubation requirements.

HUVECsHAECsPrimary hepatocytes
Metabolomics

Metabolic Flux Analysis

Chemically defined 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

Ultra-low particulate baseline supports confocal microscopy, fluorescent biosensors, and automated imaging on chip; the included phenol red indicator may contribute background fluorescence in some channels.

ConfocalBiosensorsTEER
Technical Specifications

Full technical specification

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

Physical & Chemical Parameters
Parameter Specification
Formulation [+] L-Glutamine, Phenol Red, Calcium, Magnesium / [-] Sodium Pyruvate
Appearance Red to pink, clear solution (phenol red indicator present)
pH USP <791> 7.4
Osmolality USP <785> 300 - 340 mOsm/kg H₂O
Carbon source (D-Galactose) 900 mg/L; no glucose in formulation
L-Glutamine 300 mg/L ([+])
Sodium Pyruvate Removed ([-])
Phenol Red 11 mg/L
Sterility, Purity & Safety
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 matter USP <788> Method 1 Monitored by light obscuration; not released against a numeric limit
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, 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)
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: 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
Calcium chloride dihydrate 10035-04-8 185.000
Magnesium chloride hexahydrate   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)   500.000
L-Asparagine   250.000
L-Cysteine (free base)   120.000
L-Glutamine 56-85-9 300.000
L-Histidine (free base)   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   0.100
Thiamine hydrochloride 67-03-8 1.000
OTHERS
i-Inositol 87-89-8 2.000
D-Galactose 59-23-4 900.000
Phenol red sodium salt 34487-61-1 11.000
Custom formulations: pH, galactose/glucose 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 resistivity; low trace-metal and organic carbon (TOC) content controlled during purification.

biotech

ISO Class 5 Fill & Finish

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

assignment

Micro-Batch Precision

Small-batch production for tight lot-to-lot consistency in pH, osmolality, and endotoxin control — 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

Monitored by light obscuration per USP <788> Method 1; not released against a numeric limit.

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.
CoA Request: Available at no charge for any production lot of FluxMPS™ Leibovitz's L-15 Medium w/o Sodium Pyruvate: 1X Liquid (DCP-LL15-P1X). Email support@diagnocine.com.
Product Comparison

How DCP-LL15-P1X compares

Critical differences in grade, filtration, mycoplasma barrier, water quality, and QC depth versus conventional L-15 media for MPS and microfluidic applications.

Parameter DCP-LL15-P1X (FluxMPS™) Standard L-15 (0.22 µm) Competitor L-15 (0.22 µm)
Grade Microfluidics Suitable (0.04 µm) Not applicable Not applicable
Formulation definition [+] L-Glutamine, Phenol Red, Calcium, Magnesium / [-] Sodium Pyruvate Standard Standard
Final filtration pore size 0.04 µm (40 nm) 0.22 µm 0.22 µm
Filtration stages 4 (0.1 µm ×2 + 0.04 µm ×2) 1 1
Mycoplasma-retentive filtration check_circle cancel cancel
Endotoxin (release specification) FluxMPS™ — < 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)
Particulate control (USP <788> Method 1) check_circle Monitored cancel Unspecified cancel Unspecified
Water quality Ultrapure Type 1, 18.2 MΩ·cm Unspecified Unspecified
Manufacturing QMS ISO 13485:2016 Varies Varies
Microfluidic channel validated 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 w/o Sodium Pyruvate: 1X Liquid (DCP-LL15-P1X).

Yes. DCP-LL15-P1X is engineered for organ-on-a-chip, microfluidic, and MPS applications. The 0.04 µm final filtration stage reduces sub-micron particulates that can cause microchannel clogging in standard 0.22 µm media, and the 0.1 µm stages provide mycoplasma-retentive filtration.
Four sequential stages (0.1 µm ×2 + 0.04 µm ×2), run as two dedicated prefilter/final-filter pairs, reduce particulates and provide mycoplasma-retentive filtration (approximately 0.2–0.3 µm diameter) well beyond what a single 0.22 µm pass achieves. Particulates are monitored per USP <788> Method 1 (light obscuration).
This formulation uses D-galactose (900 mg/L) as its primary carbon source rather than glucose, following the classical Leibovitz's L-15 design for CO₂-independent culture, and sodium pyruvate is omitted. If your cell line requires sodium pyruvate as an additional energy substrate, add it directly (typical range 1–5 mM), pre-filtered through a 0.1 µm syringe filter for protein-free, defined additions. Custom formulations are available at support@diagnocine.com.
No. This formulation does not contain sodium bicarbonate and is designed for CO₂-independent incubation, consistent with the classical Leibovitz's L-15 buffering strategy. If additional pH stability is desired outside a controlled atmosphere, 10–25 mM HEPES can be added on request.
Yes. DCP-LL15-P1X is a basal medium compatible with FBS (2–10%), human serum, growth factors (EGF, FGF, VEGF), and antibiotics. Pre-filter serum and other protein-containing additions through a 0.2 µm low-protein-binding PES or PVDF filter before combining; a 0.1 µm filter is appropriate only for defined, protein-free additions. Do not use a 0.04 µm filter for serum or growth factors — it will strip the protein fraction and clog rapidly.
Endotoxin is controlled per manufacturing batch, not per unit. Every batch is tested by LAL assay (USP <85> Bacterial Endotoxins Test, assay sensitivity 0.005 EU/mL) before release and must meet the specification < 0.05 EU/mL. The lot-specific result is reported on the Certificate of Analysis — request one 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>), mycoplasma filtration status, particulate monitoring (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. Leibovitz A. The growth and maintenance of tissue-cell cultures in free gas exchange with the atmosphere. Am J Hyg. 1963;78:173–180.

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