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FluxMPS™ Leibovitz's L-15 Medium: 2X Liquid

Product#: DCP-LL152X
$77.00
DCP-LL152X
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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: 2X Liquid

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

FluxMPS™ DCP-LL152X is a Microfluidics Suitable, Quadruple-stage ultra-filtered Leibovitz's L-15 2X formulation engineered for primary cells and related cell models on organ-on-a-chip (OoC) and microphysiological system (MPS) platforms. A quadruple-stage train (0.1 µm ×2 + 0.04 µm ×2) reaches a 0.04 µm final cut-off, five times finer than the 0.22 µm membranes used for conventional sterile filtration. CO2-free by design — uses D-galactose and high amino-acid buffering for atmospheric pH maintenance.

  • CO2-free by design: D-galactose energy source + high amino-acid buffering — no gas supplementation required
  • Quadruple-stage filtration (0.1 µm ×2 + 0.04 µm ×2) reaching a 0.04 µm final polish for sub-mycoplasma-range purity
  • Endotoxin release specification: < 0.05 EU/mL (LAL assay, USP <85>)
  • Formulation: [+] 1.8 g/L D-Galactose, [+] L-Glutamine (600 mg/L), [+] Sodium Pyruvate (1100 mg/L), [+] Phenol Red — orange-red colored, clear solution
  • Manufactured under an ISO 13485:2016 quality management system; final QC at Diagnocine, Totowa, NJ
  • Amino-acid buffered to pH 7.4 — validated for atmospheric, CO2-independent culture
  • 35 formulation components released per lot with full raw-material traceability
CAT. NO.
DCP-LL152X | Cell Culture Media
UNSPSC: 41116155 | Commodity: Molecular biology and cell culture growth media | (UNv260801)
Leibovitz's L-15 — 2X Liquid
  • Media familyLeibovitz's L-15 2X
  • Formulation[+] L-Glutamine, [+] Phenol Red, [+] Calcium, [+] Magnesium, [+] Sodium Pyruvate, [-] Glucose
  • Carbon sourceD-Galactose (1800 mg/L)
  • AppearanceOrange-red colored, clear solution
  • pH (USP <791>)7.4
  • Osmolality (USP <785>)Contact for specification
  • Endotoxin (USP <85>)< 0.05 EU/mL
  • Filtration0.1 µm ×2 + 0.04 µm ×2 (Quadruple-stage)
  • Storage2–8°C, away from light
  • Shelf Life12 months from date of manufacture, unopened
ISO 13485:2016 USP <85> <785> <788> RUO
Why FluxMPS™

Engineered where standard media fails

Conventional 0.22 µm–filtered Leibovitz's L-15 passes mycoplasma-sized particles and subvisible particulates that interfere with CO2-free pH maintenance and live-imaging clarity. FluxMPS™ is built to reduce these failure modes.

filter_alt

Microchannel-safe purity

0.04 µm final filtration and USP <788> Method 1 (light obscuration) particulate compliance support clear live imaging and CO2-free chip loading.

science

CO2-free by design formulation

Leibovitz's L-15 uses D-galactose (not glucose) as the primary carbon source, plus high amino-acid concentrations, for CO2-free pH buffering. This is a 2X concentrated formulation.

water_drop

Ultrapure-grade water

Type 1 water (18.2 MΩ·cm) with controlled trace-metal and organic-carbon (TOC) content, minimizing contaminants that could affect formulation stability.

shield

Low endotoxin release specification

< 0.05 EU/mL release specification — relevant where endotoxin-driven TLR4 activation could alter primary-cell phenotype.

bolt

CO2-independent design

D-galactose plus high amino-acid buffering is formulated to maintain pH under atmospheric conditions — no CO2 incubator required.

tune

Customization on demand

pH, nutrient concentrations, HEPES, and component modifications available. Contact support@diagnocine.com.

Purity Architecture

Quadruple-stage filtration system

Four serial filtration stages — two paired prefilter + final-filter passes — reaching a final 0.04 µm polish.

  1. 1

    0.1 µm Prefiltration I

    Removes large particulate, cell debris and protein aggregates; protects the first 0.04 µm cartridge.

  2. 2

    0.04 µm Final filtration I

    First 0.04 µm pass; retains sub-micron particulates and microaggregates that pass a 0.22 µm filter, including mycoplasma-range particles (0.2–0.3 µm).

  3. 3

    0.1 µm Prefiltration II

    Second, dedicated prefilter protecting the second 0.04 µm cartridge.

  4. 4

    0.04 µm Final filtration II — Polish

    Ultimate polishing filter; aseptic fill in an ISO Class 5 (Class 100) environment.

Performance vs. conventional media

5×
Cleaner than 0.22 µm media by particulate count
4
Sequential filtration passes to a 0.04 µm final pore size
Sterility & mycoplasma: No growth after 14-day incubation (USP <71>); 0.1 µm mycoplasma-retentive filtration is applied at every production stage (not 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 DCP-LL152X Quadruple-stage filtration system for Leibovitz's L-15 2X cell culture medium - 0.1 micron x2 plus 0.04 micron x2 ultra-filtration for organ-on-a-chip and microfluidic applications, Diagnocine
Figure 1. FluxMPS™ Quadruple-stage filtration system (0.1 µm ×2 + 0.04 µm ×2).
© Diagnocine® — DCP-LL152X
Applications

CO2-free live imaging and primary cell applications

FluxMPS™ DCP-LL152X — Leibovitz's L-15 2X — delivers 0.04 µm filtered purity for primary cells and related OoC applications.

Automated Bioreactors & Robotics

Next-Generation System Uptime

An optional 0.01 µm (10 nm) ultra nano-filtered MPS Grade variant is available on request for automated perfusion and robotics platforms.

  • Total Particulate Exclusion: 0.01 µm filtration removes nanoparticulate aggregates
  • Valve & Sensor Protection: Reduces micro-fouling risk in automated perfusion systems
  • Extended Perfusion Stability: Consistent nutrient delivery over long-duration culture

Inquiry required: contact support@diagnocine.com for the 0.01 µm MPS Grade variant.

Live-Cell Imaging

Open-Stage & CO2-Free Microscopy

L-15 plus galactose maintains pH without CO2 — a common base for prolonged live-cell confocal, TIRF, light-sheet, and spinning-disk imaging on open-stage microscopes.

ConfocalTIRFLight-sheetOpen-stage
Cell Biology

Primary Cell Dissociation & Transport

CO2-free L-15 is commonly used as a dissociation and transport buffer for primary cells, tissue pieces, and organoids outside the incubator.

Primary cellsOrganoidsTissue dissociation
Microfluidics

OoC Loading & Priming

CO2-independent L-15 enables chip loading, priming, and cell seeding outside incubators without pH drift during chip assembly.

OoC loadingChip primingCell seeding
In Vivo Studies

In Vivo Imaging & Intravital Microscopy

L-15 is used as a superfusion medium for intravital microscopy, supporting pH maintenance in open tissue preparations without CO2 during surgical and imaging procedures.

IntravitalSuperfusionIn vivo
Metabolomics

CO2-Free Metabolic Studies

The galactose-based energy source supports metabolic studies without CO2 interference; galactose is commonly used to force oxidative phosphorylation in metabolically flexible cells.

OXPHOSGalactose forcingMetabolomics
Neuroscience

Acute Brain Slice & Neuron Imaging

CO2-free L-15 supports neuronal viability in acute brain slice preparations and dissociated neuron imaging without carbogen (95% O2/5% CO2) gassing.

Brain slicesPrimary neuronsNeuronal imaging
Technical Specifications

Analytical release specifications

Every lot released against the specification matrix below. CoA available on request: support@diagnocine.com.

Physical & Chemical Parameters
Parameter Specification
Formulation [+] L-Glutamine, [+] Phenol Red, [+] Calcium, [+] Magnesium, [+] Sodium Pyruvate, [-] Glucose
Appearance Orange-red colored, clear solution
Carbon source D-Galactose — 1800 mg/L (not glucose)
L-Glutamine 600 mg/L
Sodium Pyruvate 1100 mg/L
Phenol Red 22 mg/L (phenol red sodium salt)
pH USP <791> 7.4
Osmolality USP <785> Contact for specification
Total ingredients 35 components across four composition groups
Sterility, Purity & Safety Parameters
Parameter Specification
Endotoxin USP <85> BET < 0.05 EU/mL
Sterility USP <71> No growth / 14 days
Mycoplasma 0.1 µm mycoplasma-retentive filtration (not tested per lot)
Particulate ≥10 µm USP <788> Method 1 NMT 25/mL
Particulate ≥25 µm USP <788> Method 1 NMT 3/mL
Water purity Type 1, 18.2 MΩ·cm
Manufacturing std. ISO 13485:2016
Fill environment ISO Class 5 (Class 100)
Storage, Handling & Logistics
Parameter Specification
Storage temperature 2–8°C, away from light
Freeze-thaw Do not freeze
Shelf life 12 months from date of manufacture, unopened
Shipping condition Cold pack
CO2 requirement CO2-independent by design — D-galactose and high amino-acid buffering maintain pH without gas supplementation
Raw Materials & Regulatory Traceability
Parameter Specification
Raw material grade Reagent / cell culture grade
Traceability Full lot traceability per ISO 13485
Manufacturing QMS ISO ISO 13485:2016 certified
UNSPSC 41116155 — Molecular biology and cell culture growth media (UNv260801)
Regulatory alignment 21 CFR Part 820 (QMSR) aligned
Production method Micro-batch, per-lot QC release
Intended use Research Use Only (RUO)

Pack sizes available: 500 mL, 1000 mL.

Formulation

Full composition (mg/L)

Leibovitz's L-15 2X: 35 components verified per lot with CAS numbers for raw-material traceability. L-15 uses D-galactose (not glucose) as the primary carbon source and high amino-acid concentrations for CO2-free pH buffering. This is a 2X concentrated formulation.

Component CAS Number mg/L
INORGANIC SALTS
Calcium chloride dihydrate 10035-04-8 370.000
Magnesium chloride hexahydrate 7791-18-6 400.000
Magnesium sulfate anhydrous 7487-88-9 195.440
Potassium chloride 7447-40-7 800.000
Potassium phosphate monobasic 7778-77-0 120.000
Sodium chloride 7647-14-5 16000.000
Sodium dihydrogen phosphate anhydrous 7558-80-7 380.240
Component CAS Number mg/L
AMINO ACIDS
L-Alanine 56-41-7 450.000
Glycine 56-40-6 400.000
L-Arginine (free base) 74-79-3 1000.000
L-Asparagine 70-47-3 500.000
L-Cysteine (free base) 52-90-4 240.000
L-Glutamine 56-85-9 600.000
L-Histidine (free base) 71-00-1 500.000
L-Isoleucine 73-32-5 500.000
L-Leucine 61-90-5 250.000
L-Lysine hydrochloride 657-27-2 188.000
L-Methionine 63-68-3 150.000
L-Phenylalanine 63-91-2 250.000
L-Serine 56-45-1 400.000
L-Threonine 72-19-5 600.000
L-Tryptophan 73-22-3 40.000
L-Tyrosine disodium salt 69847-45-6 552.320
L-Valine 72-18-4 200.000
Component CAS Number mg/L
VITAMINS
Choline chloride 67-48-1 2.000
D-Ca-Pantothenate 137-08-6 2.000
Folic acid 59-30-3 2.000
Nicotinamide 98-92-0 2.000
Pyridoxine hydrochloride 58-56-0 2.000
Riboflavin-5-phosphate sodium salt 130-40-5 0.200
Thiamine hydrochloride 67-03-8 2.000
OTHERS
D-Galactose 59-23-4 1800.000
Sodium pyruvate 113-24-6 1100.000
Phenol red sodium salt 34487-61-1 22.000
i-Inositol 87-89-8 4.000
Custom formulation: Contact support@diagnocine.com for DCP-LL152X modifications.
Quality Assurance

Manufacturing & compliance

Every FluxMPS™ product is manufactured and released under a multi-layer quality system.

verified

ISO 13485:2016 Quality Management

Manufactured under ISO 13485:2016-certified facilities. Final QA at Diagnocine R&D Center, Totowa, NJ, USA.

water_drop

Ultrapure Type 1 Water

18.2 MΩ·cm, with controlled trace-metal and organic-carbon content.

biotech

ISO Class 5 Fill & Finish

Aseptic fill in validated ISO Class 5 (Class 100) laminar-flow workstations.

assignment

Micro-Batch Precision

Small-batch, per-lot tested — no blending; Certificate of Analysis available for every lot.

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.

Endotoxin — USP <85> BET

LAL assay; release specification < 0.05 EU/mL per batch.

Particulate — USP <788> Method 1

Light obscuration count: NMT 25/mL (≥10 µm), NMT 3/mL (≥25 µm).

Osmolality — USP <785>

Target: Contact for specification.

Documentation & CoA

Full CoA with raw-material traceability available on request.

Certificate of Analysis: Request for any DCP-LL152X lot at support@diagnocine.com.
Product Comparison

How DCP-LL152X compares

FluxMPS™ DCP-LL152X vs. conventional 0.22 µm–filtered Leibovitz's and standard formulations.

Parameter DCP-LL152X (FluxMPS™) Conventional Leibovitz's L-15
(0.22 µm filtered)		 Standard DMEM/RPMI
(0.22 µm filtered)
Grade Microfluidics Suitable Not specified Not specified
CO2-free design (galactose-based) check_circle Yes check_circle Yes cancel No
Final filtration pore size 0.04 µm 0.22 µm 0.22 µm
Number of filtration stages 4 (Quadruple) 1 1
Mycoplasma-retentive filtration check_circle Yes (0.1/0.04 µm) cancel No cancel No
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 tested check_circle Yes cancel Not specified cancel Not specified
Water quality Type 1, 18.2 MΩ·cm Not specified Not specified
Manufacturing QMS ISO 13485:2016 Not specified Not specified
Microfluidic channel compatibility check_circle Microfluidics Suitable cancel Risk of clogging cancel Risk of clogging
Custom formulation available check_circle Yes Not specified Not specified

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™ DCP-LL152X — Leibovitz's L-15 2X.

DCP-LL152X is processed through a Quadruple-stage filtration system reaching a 0.04 µm final pore size. Leibovitz's L-15's CO2-free design makes it well suited to chip loading, priming, open-stage imaging, and atmospheric OoC platforms where CO2 control is impractical.
 
Leibovitz's L-15 was designed for CO2-free culture — it uses D-galactose (instead of glucose) and sodium pyruvate as energy sources, because these metabolites can support energy metabolism without generating CO2 as a buffering byproduct. Combined with high amino-acid concentrations (notably alanine and arginine) that substitute for bicarbonate buffering capacity, L-15 is formulated to maintain pH near 7.4 under atmospheric conditions without CO2. It is commonly used for primary cell dissociation, in vivo studies, transport buffers, and live imaging on open-stage microscopes. This is a 2X formulation intended for use diluted or with concentrated supplements.
CO2-independent by design — Leibovitz's L-15 uses D-galactose and high amino-acid buffering for CO2-free pH maintenance. No gas supplementation is required.
Yes. Add FBS (5–10%), serum-free supplements, growth factors, or antibiotics as required. Filter additions through a 0.2 µm low-protein-binding PES or PVDF membrane before adding to the medium — do not use a 0.04 µm membrane for serum or protein-containing additions. Contact support@diagnocine.com for custom co-formulation.
FluxMPS™ DCP-LL152X is released to meet < 0.05 EU/mL by LAL assay (USP <85>). Endotoxin is controlled per manufacturing batch: every batch is tested before release and must meet this specification. Low endotoxin is relevant for primary cells, where endotoxin can activate TLR4 and alter phenotype or differentiation outcomes.
Yes. A full CoA per lot covers: appearance, pH (USP <791>), osmolality (USP <785>), sterility (USP <71>), endotoxin (USP <85>), mycoplasma-retentive filtration status, particulate count (USP <788> Method 1), and raw-material traceability. Request at support@diagnocine.com.
Scientific References

Supporting literature

Key publications relevant to Leibovitz's L-15 2X in CO2-free live-cell imaging, primary cell culture, and OoC applications.

  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.a120329
  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. Novak R, et al. Robotic fluidic coupling and interrogation of multiple vascularized organ chips. Nat Biomed Eng. 2020;4:407–420. doi:10.1038/s41551-019-0497-x
  5. Jang KJ, et al. Human kidney proximal tubule-on-a-chip. Integr Biol. 2013;5:1119–1129. doi:10.1039/c3ib40049b
  6. Schimek K, et al. Integrating biological vasculature into a multi-organ-chip microsystem. Lab Chip. 2013;13:3588–3598. doi:10.1039/c3lc50217a
  7. Luni C, et al. High-efficiency cellular reprogramming with microfluidics. Nat Methods. 2016;13:446–452. doi:10.1038/nmeth.3832
  8. Sung JH, et al. Microfabricated mammalian organ systems. Lab Chip. 2013;13:1201–1212. doi:10.1039/c3lc41017j

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