FluxMPS™ Dulbecco’s Modified Eagle Medium (DMEM), High Glucose w/ L-Alanyl-Glutamine: 1X Liquid

Product#: DCP-DMEMYA1X
$44.00
DCP-DMEMYA1X
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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™ Dulbecco’s Modified Eagle Medium (DMEM), High Glucose w/ L-Alanyl-Glutamine: 1X Liquid

Contains Sodium Bicarbonate Contains Phenol Red Contains Calcium Contains Magnesium Contains Glucose Contains Sodium Pyruvate

FluxMPS™ DCP-DMEMYA1X is a Microfluidics Suitable, ultra-filtered DMEM High Glucose — L-Alanyl-Glutamine formulation engineered for long-duration organ-on-a-chip and bioreactor perfusion, where a stable, ammonia-free nitrogen source is essential. 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. Formulation: [+] High Glucose (4500 mg/L), [+] L-Alanyl-Glutamine (dipeptide), [+] Sodium Pyruvate, [+] Sodium Bicarbonate.

  • L-Alanyl-L-Glutamine (dipeptide, CAS 39537-23-0) — stable at 37°C, does not degrade to pyrrolidone-5-carboxylic acid and ammonia the way free L-glutamine does
  • No ammonia accumulation — avoids ammonia-driven growth inhibition and glycosylation artefacts during long-duration perfusion
  • Cleaved to L-glutamine + L-alanine by cell-surface dipeptidases — bioequivalent nitrogen source to free L-glutamine
  • Suited to organ-on-a-chip, bioreactor perfusion, and any culture lasting more than 7 days where glutamine stability matters
  • Quadruple-stage filtration: 0.1 µm Prefiltration I → 0.04 µm Final filtration I → 0.1 µm Prefiltration II → 0.04 µm Final filtration II — Polish
  • Endotoxin release specification < 0.05 EU/mL (LAL, USP <85>), tested per manufacturing batch
  • Manufactured under an ISO 13485:2016 quality management system with ISO Class 5 (Class 100) aseptic fill
  • Custom formulation modifications available on request — contact support@diagnocine.com
CAT. NO.
DCP-DMEMYA1X | Cell Culture Media UNSPSC: 41116155 | Commodity: Molecular biology and cell culture growth media | (UNv260801)
Dulbecco’s Modified Eagle Medium (DMEM), High Glucose w/ L-Alanyl-Glutamine: 1X Liquid
  • Glucose4500 mg/L (4.5 g/L, High Glucose)
  • Key featureL-Alanyl-Glutamine (dipeptide)
  • Formulation[+] Sodium Bicarbonate, [+] Phenol Red, [+] Calcium, [+] Magnesium, [+] Glucose, [+] Sodium Pyruvate
  • AppearanceRed-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
  • Storage2–8°C, away from light
  • Shelf Life12 months from date of manufacture, unopened
ISO 13485:2016 USP <85> <785> <788> RUO
Why FluxMPS™

Stable glutamine — no degradation, no ammonia accumulation

Standard DMEM contains free L-glutamine, which spontaneously degrades in aqueous solution to pyrrolidone-5-carboxylic acid and ammonia at 37°C (half-life approximately 3 weeks at 4°C; days at 37°C). Ammonia accumulation inhibits cell growth and alters glycosylation, confounding metabolic assays. L-Alanyl-L-Glutamine (dipeptide, CAS 39537-23-0) is a stable dipeptide that does not degrade this way — it is cleaved to L-glutamine + L-alanine by dipeptidases at the cell surface, providing a sustained, stable nitrogen source. FluxMPS™ pairs this stable-glutamine formulation with 0.04 µm final filtration for long-duration OoC perfusion where glutamine stability is critical.

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Microchannel-safe purity

0.04 µm final filtration; USP <788> particulate compliance supports safe perfusion in chip geometries, including sub-100 µm channels.

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Precise formulation control

L-Alanyl-Glutamine in place of free L-glutamine — a defined substitution enabling research applications that require a stable, non-degrading nitrogen source.

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Ultrapure-grade water

Ultrapure Type 1 water (18.2 MΩ·cm) with controlled trace-metal and organic-carbon (TOC) content, reducing background contributed by the water itself.

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Low endotoxin release specification

< 0.05 EU/mL endotoxin release specification, tested by LAL assay (USP <85>) per manufacturing batch.

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High-glucose energy support

4.5 g/L glucose sustains the energy demands of glycolytically active cell types and extended perfusion protocols.

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Customization on demand

pH, glucose, salts, and additional component modifications available. Contact support@diagnocine.com.

Purity Architecture

Quadruple-stage filtration system

Four serial filtration stages, run as two prefilter-plus-final-filter pairs, reaching a final 0.04 µm polish under aseptic conditions — delivering ultra-low particulate levels beyond what conventional 0.22 µm filtered media can achieve.

  1. 1

    0.1 µm Prefiltration I

    Removes large aggregates, cell debris and protein clumps; protects the first 0.04 µm final-filter cartridge from fouling.

  2. 2

    0.04 µm Final filtration I

    First 0.04 µm final-filtration pass; retains sub-micron particulates and microaggregates that pass a conventional 0.22 µm filter. Together with the upstream 0.1 µm stage, this provides mycoplasma-retentive filtration (organisms in the 0.2–0.3 µm range); not tested per lot.

  3. 3

    0.1 µm Prefiltration II

    Second dedicated prefilter, protecting the second 0.04 µm final-filter cartridge and providing redundant large-particulate removal.

  4. 4

    0.04 µm Final filtration II — Polish

    Ultimate 0.04 µm polishing filter; aseptic fill & finish.

Performance vs. conventional media

5×
Cleaner than 0.22 µm media by particulate count
0.04
µm Final pore size across four filtration stages
Sterility & Mycoplasma: No growth after 14-day incubation (USP <71>). Mycoplasma risk is controlled by 0.1 µm and 0.04 µm mycoplasma-retentive filtration at every stage; lots are not individually tested for mycoplasma unless otherwise specified.
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-DMEMYA1X Dulbecco's Modified Eagle Medium (DMEM), High Glucose w/ L-Alanyl-Glutamine: 1X Liquid ? Quadruple-stage filtration system: 0.1 μm Prefiltration I, 0.04 μm Final filtration I (mycoplasma barrier), 0.1 μm Prefiltration II, 0.04 μm Final filtration II Polish ? Microfluidics Suitable DMEM High Glucose L-Alanyl-Glutamine for organ-on-a-chip | Diagnocine
Figure 1. FluxMPS™ Quadruple-stage filtration system (0.1 µm ×2 + 0.04 µm ×2) used to produce DCP-DMEMYA1X.
© Diagnocine® — DCP-DMEMYA1X
Applications

Specialized applications requiring stable-glutamine DMEM

FluxMPS™ DCP-DMEMYA1X is designed for research protocols where L-Alanyl-Glutamine stability is essential — combined with Microfluidics Suitable filtration purity for organ-on-a-chip and microfluidic platform compatibility.

Automated Bioreactors & Robotics

Next-Generation System Uptime

An optional 0.01 µm (10 nm) MPS Grade variant is available for automated bioreactor perfusion and robotic liquid handlers — the separate ultra nano-filtered tier described in the grade note above.

  • Total Particulate Exclusion: 10 nm filtration removes nanoparticulate aggregates invisible to standard QC
  • Valve & Sensor Protection: Reduces micro-fouling risk in automated perfusion circuits
  • Extended Perfusion Stability: Consistent nutrient delivery over long-duration culture

Inquiry Required: Contact support@diagnocine.com for the 0.01 µm MPS Grade variant.

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Organ-on-a-Chip & MPS

0.04 µm filtration reduces microchannel clogging risk. L-Alanyl-Glutamine formulation delivered with low particulate content for specialized OoC protocols.

OoCMPSToCBoC
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Organ-on-a-Chip Long-Duration Perfusion

FluxMPS™ DCP-DMEMYA1X delivers stable L-Alanyl-Glutamine nutrition with Microfluidics Suitable filtration purity for demanding long-duration perfusion platforms.

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Bioreactor Continuous Culture

Ammonia-free nitrogen delivery over extended culture periods supports continuous bioreactor operation without periodic glutamine re-dosing.

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iPSC Differentiation

Stable nitrogen source and low-particulate filtration support extended differentiation protocols sensitive to metabolic byproduct accumulation.

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Glycoprotein Production

Avoiding ammonia accumulation helps preserve consistent N-glycosylation patterns in glycoprotein-producing cell lines over long culture runs.

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CHO Long-Term Culture

Stable-glutamine formulation reduces ammonia-driven growth inhibition in CHO cultures maintained over multi-day to multi-week production runs.

Technical Specifications

Analytical release specifications

Every lot released against the full specification matrix. CoA: support@diagnocine.com.

Physical & Chemical Parameters
Parameter Specification
Formulation [+] Sodium Bicarbonate, [+] Phenol Red, [+] Calcium, [+] Magnesium, [+] Glucose, [+] Sodium Pyruvate
Appearance Red-colored, clear solution
Glucose 4500 mg/L (4.5 g/L, High Glucose)
Key feature L-Alanyl-Glutamine (dipeptide, 862 mg/L)
pH USP <791> 7.4
Osmolality USP <785> Contact for specification
L-Glutamine (free) Not added — replaced by L-Alanyl-Glutamine dipeptide
Sodium Pyruvate 110 mg/L
Phenol Red 15.900 mg/L (phenol red sodium salt)
Total ingredients 33 (7 Inorganic Salts, 15 Amino Acids, 8 Vitamins, 3 Others)
Sterility, Purity & Safety
Parameter Specification
Endotoxin USP <85> BET < 0.05 EU/mL (batch release specification; see Manufacturing & Compliance)
Sterility USP <71> No growth / 14 days
Mycoplasma Controlled by 0.1 µm + 0.04 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 Approximately 10% CO2 (calculated from 3700 mg/L sodium bicarbonate to maintain pH 7.4; validate per incubator and cell line)
Pack sizes 500 mL, 1000 mL
Raw Materials & Regulatory
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)
Formulation

Full composition (mg/L)

DMEM High Glucose — L-Alanyl-Glutamine: 33 ingredients verified per lot with CAS numbers for raw-material traceability. L-Alanyl-L-Glutamine (dipeptide, CAS 39537-23-0) replaces free L-glutamine at an equivalent molar nitrogen contribution. Do not add additional free L-glutamine unless specifically required.

INORGANIC SALTS
Component CAS Number mg/L
INORGANIC SALTS
Calcium chloride dihydrate 10035-04-8 265.000
Ferric nitrate nonahydrate 7782-61-8 0.100
Magnesium sulfate anhydrous 7487-88-9 97.720
Potassium chloride 7447-40-7 400.000
Sodium bicarbonate 144-55-8 3700.000
Sodium chloride 7647-14-5 6400.000
Sodium dihydrogen phosphate anhydrous 7558-80-7 109.000
AMINO ACIDS
Component CAS Number mg/L
AMINO ACIDS
Glycine 56-40-6 30.000
L-Arginine hydrochloride 1119-34-2 84.000
L-Cystine dihydrochloride 30925-07-6 62.570
L-Alanyl-Glutamine 39537-23-0 862.000
L-Histidine hydrochloride monohydrate 5934-29-2 42.000
L-Isoleucine 73-32-5 105.000
L-Leucine 61-90-5 105.000
L-Lysine hydrochloride 657-27-2 146.000
L-Methionine 63-68-3 30.000
L-Phenylalanine 63-91-2 66.000
L-Serine 56-45-1 42.000
L-Threonine 72-19-5 95.000
L-Tryptophan 73-22-3 16.000
L-Tyrosine Disodium Salt dihydrate 69847-15-0 103.790
L-Valine 72-18-4 94.000
VITAMINS AND OTHERS
Component CAS Number mg/L
VITAMINS
Choline chloride 67-48-1 4.000
D-Ca-Pantothenate 137-08-6 4.000
Folic acid 59-30-3 4.000
Nicotinamide 98-92-0 4.000
Pyridoxal hydrochloride 65-22-5 4.000
Riboflavin 83-88-5 0.400
Thiamine hydrochloride 67-03-8 4.000
i-Inositol 87-89-8 7.200
OTHERS
D-Glucose 50-99-7 4500.000
Phenol red sodium salt 34487-61-1 15.900
Sodium pyruvate 113-24-6 110.000
Custom formulation: Contact support@diagnocine.com for DCP-DMEMYA1X modifications — component additions, pH changes, or nutrient adjustments.
Quality Assurance

Manufacturing & compliance

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

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ISO 13485:2016 Quality Management

Manufactured under an ISO 13485:2016–certified quality system. Final QA at the Diagnocine R&D Center, Totowa, NJ, USA.

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Ultrapure Type 1 Water

18.2 MΩ·cm with controlled trace-metal and TOC content.

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ISO Class 5 Fill & Finish

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

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Micro-Batch Precision

Small-batch, per-lot tested — Certificate of Analysis available for every lot.

Endotoxin — USP <85> BET

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

Particulate — USP <788> Method 1

Light obscuration: 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 for every lot on request.

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-DMEMYA1X compares

FluxMPS™ DCP-DMEMYA1X vs. conventional 0.22 µm–filtered DMEM High Glucose formulations.

Parameter DCP-DMEMYA1X (FluxMPS™) Conventional DMEM HG
(0.22 µm filtered)
Standard DMEM HG
(0.22 µm filtered)
Grade Microfluidics Suitable (0.04 µm final cut-off) Standard grade (no filtration tier designation) Standard grade (no filtration tier designation)
Stable-glutamine formulation (L-Alanyl-Glutamine, ammonia-free) check_circle Yes cancel No 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) 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)
USP <788> particulate compliance check_circle Method 1 tested cancel Not specified cancel Not specified
Water quality Type 1, 18.2 MΩ·cm Purified water Purified water
Manufacturing QMS ISO 13485:2016 ISO 9001 or none ISO 9001 or none
Microfluidic channel compatibility check_circle Microfluidics Suitable cancel Higher clogging risk cancel Higher clogging risk
Custom formulation check_circle Available cancel Fixed cancel Fixed

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-DMEMYA1X — DMEM High Glucose with L-Alanyl-Glutamine.

Yes. DCP-DMEMYA1X is processed through a Quadruple-stage filtration system reaching a 0.04 µm final pore size, delivering low particulate levels for MPS, OoC, ToC and LoC platforms. The L-Alanyl-Glutamine formulation combines mycoplasma-retentive filtration with a < 0.05 EU/mL endotoxin release specification for demanding on-chip culture.
 
L-Alanyl-L-Glutamine is a stable dipeptide where L-alanine is covalently linked to L-glutamine, blocking the spontaneous cyclization that converts free glutamine to pyrrolidone-5-carboxylic acid and ammonia. The dipeptide is stable for the full shelf life of the medium at 4°C and remains stable during long-duration perfusion at 37°C. At the cell surface, dipeptidases cleave the alanyl-glutamine bond, releasing free glutamine and alanine — cells receive the same bioavailable nitrogen source as from free L-glutamine, without the ammonia byproduct. In organ-on-a-chip perfusion experiments lasting days to weeks, this avoids ammonia-driven growth inhibition (IC50 approximately 2 mM NH4+ for most mammalian cells) and helps preserve consistent N-glycosylation patterns in glycoprotein-producing cells. Do not add additional free L-glutamine unless your protocol specifically requires it.
This formulation contains 3700 mg/L sodium bicarbonate. Maintaining pH 7.4 with this bicarbonate concentration requires approximately 10% CO2, not the 5% CO2 associated with lower-bicarbonate formulations. Validate the CO2 setpoint against your own incubator and cell line before use.
Yes. Add FBS (typically 5–10%), serum-free supplements, growth factors, antibiotics, or custom nutrients as required. When filtering serum-containing or protein-containing additions after supplementation, use a 0.2 µm low-protein-binding PES or PVDF filter — a 0.04 µm membrane will strip serum of the proteins and lipoproteins that make it functional and is not appropriate for this purpose. Contact support@diagnocine.com for custom co-formulation.
Every manufacturing batch of DCP-DMEMYA1X is tested by LAL assay (USP <85>, assay sensitivity 0.005 EU/mL) and must meet the release specification of < 0.05 EU/mL before release. This is a batch-level release specification, not a per-unit certificate; see the Product Comparison section for published figures from other suppliers.
Yes. A full CoA per lot covers: appearance, pH (USP <791>), osmolality (USP <785>), sterility (USP <71>), endotoxin (USP <85>), mycoplasma control status, particulate count (USP <788> Method 1), and raw-material traceability, including lot number and expiry. Request at support@diagnocine.com.
Scientific References

Supporting literature

Key publications supporting the research applications of FluxMPS™ DCP-DMEMYA1X.

  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. Ozturk SS, Riley MR, Palsson BO. Effects of ammonia and lactate on hybridoma growth, metabolism, and antibody production. Biotechnol Bioeng. 1992;39:418–431. doi:10.1002/bit.260390408
  4. Christie A, Butler M. Glutamine-based dipeptides are utilized by mammalian cells by extracellular hydrolysis catalyzed by a specific peptidase. J Biotechnol. 1994;37:277–290. doi:10.1016/0168-1656(94)90032-9
  5. 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
  6. Jang KJ, et al. Human kidney proximal tubule-on-a-chip for drug transport and nephrotoxicity assessment. Integr Biol. 2013;5:1119–1129. doi:10.1039/c3ib40049b
  7. Andersen DC, Goochee CF. The effect of ammonia on the O-linked glycosylation of granulocyte colony-stimulating factor produced by Chinese hamster ovary cells. Biotechnol Bioeng. 1995;47:96–105. doi:10.1002/bit.260470112
  8. Schimek K, et al. Integrating biological vasculature into a multi-organ-chip microsystem. Lab Chip. 2013;13:3588–3598. doi:10.1039/c3lc50217a
  9. Sung JH, et al. Microfabricated mammalian organ systems and their integration into models of whole animals and humans. Lab Chip. 2013;13:1201–1212. doi:10.1039/c3lc41017j

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