FluxMPS™ RPMI 1640 Medium w/o L-Glutamine, Sodium Pyruvate, Sodium Bicarbonate: 1X Liquid

Product#: DCP-RPMI-QPB1X
$34.10
DCP-RPMI-QPB1X
Availability:
Ships in 1-2 Weeks

warning For Research Use Only (RUO). Not intended for clinical, diagnostic, or therapeutic use in humans.
verified ISO 13485 Certified Manufacturing

FluxMPS™ RPMI 1640 Medium w/o L-Glutamine, Sodium Pyruvate, Sodium Bicarbonate: 1X Liquid

Contains Phenol Red Contains Calcium Contains Magnesium Contains 2.0 g/L Glucose Without L-Glutamine Without Sodium Bicarbonate Without Sodium Pyruvate

FluxMPS™ DCP-RPMI-QPB1X is a Microfluidics Suitable, quadruple-stage ultra-filtered (0.1 µm ×2 + 0.04 µm ×2) RPMI 1640 formulation supplying 2.0 g/L glucose as the sole added carbon source, with L-glutamine, sodium pyruvate, and sodium bicarbonate all left out so investigators can define their own metabolic and buffering conditions. 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.

  • Carbon source: 2000 mg/L (2.0 g/L) D-glucose — the sole added energy substrate in this triple-omission formulation
  • Formulated without L-glutamine, sodium pyruvate, and sodium bicarbonate for maximum user-defined metabolic and buffer control
  • Contains 1.0 mg/L reduced glutathione — antioxidant support for redox-sensitive lymphocyte and hematopoietic cell types
  • Quadruple-stage filtration (0.1 µm ×2 + 0.04 µm ×2) reaching a 0.04 µm final pore size, with an endotoxin release specification of < 0.05 EU/mL (LAL, USP <85>)
  • CO₂-independent formulation; supplement with 15–25 mM HEPES for pH buffering under atmospheric conditions
  • Manufactured under an ISO 13485:2016 quality management system, with Ultrapure Type 1 water (18.2 MΩ·cm) and aseptic ISO Class 5 fill & finish
  • 38 formulation components verified per lot across inorganic salts, amino acids, vitamins, and other constituents, with full CAS traceability
CAT. NO.
DCP-RPMI-QPB1X | Cell Culture Media UNSPSC: 41116155 | Commodity: Molecular biology and cell culture growth media | (UNv260801)
RPMI 1640 — 1X Liquid (w/o L-Glutamine, Sodium Pyruvate, Sodium Bicarbonate)
  • Media familyRPMI 1640
  • Formulation[+] Phenol Red, Calcium, Magnesium, 2.0 g/L Glucose | [-] L-Glutamine, Sodium Bicarbonate, Sodium Pyruvate
  • L-GlutamineNone / Not added
  • Sodium PyruvateNone / Not added
  • pH (USP <791>)7.4
  • Osmolality (USP <785>)230–270 mOsm/kg H₂O
  • Endotoxin (USP <85>)< 0.05 EU/mL
  • Filtration0.1 µm ×2 + 0.04 µm ×2 (Quadruple-stage)
  • Storage2–8°C, protect from light
  • Shelf Life12 months from date of manufacture, unopened
Available sizes: 500 mL, 1000 mL
ISO 13485:2016 USP <85> <785> <788> RUO
Why FluxMPS™

Engineered where standard media fails

Conventional 0.22 µm–filtered RPMI passes subvisible particulates and mycoplasma-sized organisms that can activate TLR4 signaling and confound immune cell assays. FluxMPS™ is built to reduce those failure modes.

filter_alt

Microchannel-safe purity

0.04 µm final filtration and USP <788> Method 1 particulate compliance keep suspension immune cell channels free of clogging debris.

target

Total metabolic control

User-defined carbon source: only 2.0 g/L glucose is provided, with glutamine, pyruvate, and bicarbonate left to the investigator for precise control of lymphocyte metabolic-flux experiments.

water_drop

Ultrapure-grade water

Ultrapure Type 1 water (18.2 MΩ·cm) minimizes trace-metal and organic-carbon content entering the formulation.

visibility

Low background for imaging

0.04 µm filtration minimizes the subvisible particulate baseline that can scatter light and interfere with confocal microscopy and biosensor-based readouts, independent of formulation color.

science

Rich, stable nutrient profile

38 verified components across amino acids, vitamins, inorganic salts, and other constituents — including reduced glutathione for redox-sensitive hematopoietic cell types — released on a per-lot micro-batch basis.

tune

Customization on demand

pH, HEPES, glucose concentration, and re-addition of glutamine, pyruvate, or bicarbonate available on request. Contact support@diagnocine.com.

Purity Architecture

Quadruple-stage filtration system

Four serial filtration passes — two dedicated prefilter/final-filter pairs — reaching a final 0.04 µm polish.

  1. 1

    0.1 µm Prefiltration I

    Large particulate, cell debris, and protein aggregate removal; 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.

  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 & finish in a validated ISO Class 5 (Class 100) environment.

Performance vs. conventional media

5×
Cleaner than 0.22 µm media by particulate count
0.04
µm final pore size across 4 filtration passes
Sterility: No growth after 14-day incubation (USP <71>).
Mycoplasma control: 0.1 µm mycoplasma-retentive filtration is applied during processing (not tested per lot). Mycoplasma range from approximately 0.2–0.3 µm in diameter.
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-RPMI-QPB1X RPMI 1640 quadruple-stage filtration system, 0.1 micron x2 plus 0.04 micron x2, for microfluidic and organ-on-a-chip cell culture applications, Diagnocine
Figure 1. FluxMPS™ Quadruple-stage filtration system (0.1 µm ×2 + 0.04 µm ×2).
© Diagnocine® — DCP-RPMI-QPB1X
Applications

Immune cell OoC and hematopoietic applications

FluxMPS™ DCP-RPMI-QPB1X — RPMI 1640 — delivers 0.04 µm filtered purity for hematopoietic and lymphocyte cell models and related microfluidic applications.

Automated Bioreactors & Robotics

Next-Generation System Uptime

An optional 0.01 µm (10 nm) MPS Grade variant of this formulation is available on request for automated perfusion and robotic handling systems.

  • Total Particulate Exclusion: 10 nm 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.

Immunology

T Cell & Lymphocyte Culture

RPMI 1640 is the standard base medium for primary T cells, B cells, NK cells, and monocytes. 0.04 µm filtration reduces particulate-driven TLR4 activation artifacts in immune assays.

T cellsB cellsNK cellsPBMC
Cancer Biology

Leukemia & Lymphoma Lines

RPMI supports NCI-60 hematopoietic cancer lines, Jurkat, Raji, K562, and HL-60 — models where a DMEM background would alter proliferation and signaling.

JurkatRajiK562HL-60
Microfluidics

Immune Cell OoC

0.04 µm filtered RPMI for tumor-immune interaction chips, vascular-immune OoC, and lymph-node-on-chip models, where particle-free media reduces TLR4 activation risk.

Tumor-immune chipLymph node OoCMPS
Immunotherapy

CAR-T & TIL Expansion

A low endotoxin release specification (<0.05 EU/mL) supports CAR-T manufacturing and TIL expansion protocols where minimizing LPS-driven T cell activation artifacts is a priority.

CAR-TTILTCR-T
Metabolomics

Immune Cell Metabolic Flux

Defined RPMI base for lymphocyte glycolysis and OXPHOS flux studies and ¹³C isotope tracing of T cell activation metabolism. Not compatible with Agilent Seahorse XF assays, which require bicarbonate-free, phenol-red-free medium — this formulation contains phenol red.

¹³C tracingGlycolysisOXPHOS
Live-Cell Imaging

Flow Cytometry & Confocal

Ultra-low particulate 0.04 µm filtration reduces background scatter for flow cytometry, ELISA, and immune cell confocal imaging. A phenol-red-free custom variant is available on request for fluorescence-sensitive assays.

Flow cytometryConfocalELISA
Technical Specifications

Analytical release specifications

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

Physical & Chemical Parameters
Parameter Specification
Formulation [+] Phenol Red, Calcium, Magnesium, 2.0 g/L Glucose | [-] L-Glutamine, Sodium Bicarbonate, Sodium Pyruvate
Appearance Orange-colored, clear solution
Glucose 2000 mg/L (2.0 g/L)
pH USP <791> 7.4
Osmolality USP <785> 230–270 mOsm/kg H₂O
Total ingredients 38
Sterility, Purity & Safety Parameters
Parameter Specification
Endotoxin USP <85> BET < 0.05 EU/mL (batch release spec)
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 Ultrapure 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, protect from light
Freeze-thaw Do not freeze
Shelf life 12 months from date of manufacture, unopened
Shipping condition Cold pack
CO₂ requirement CO₂-independent (bicarbonate-free); supplement with 15–25 mM HEPES for pH buffering
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)
Formulation

Full composition (mg/L)

RPMI 1640: 38 ingredients verified per lot with CAS numbers for full raw-material traceability, including reduced glutathione for redox-sensitive lymphocyte and hematopoietic cell culture.

Component CAS Number mg/L
INORGANIC SALTS
Calcium nitrate tetrahydrate 13477-34-4 100.000
Magnesium sulfate anhydrous 7487-88-9 48.840
Potassium chloride 7447-40-7 400.000
Sodium chloride 7647-14-5 6000.000
Sodium phosphate dibasic anhydrous 7558-79-4 800.000
Component CAS Number mg/L
AMINO ACIDS
Glycine 56-40-6 10.000
L-Arginine hydrochloride 1119-34-2 241.000
L-Asparagine 70-47-3 50.000
L-Aspartic acid 56-84-8 20.000
L-Cystine dihydrochloride 30925-07-6 65.200
L-Glutamic acid 56-86-0 20.000
L-Histidine hydrochloride monohydrate 5934-29-2 20.960
L-Hydroxyproline 51-35-4 20.000
L-Isoleucine 73-32-5 50.000
L-Leucine 61-90-5 50.000
L-Lysine hydrochloride 657-27-2 40.000
L-Methionine 63-68-3 15.000
L-Phenylalanine 63-91-2 15.000
L-Proline 147-85-3 20.000
L-Serine 56-45-1 30.000
L-Threonine 72-19-5 20.000
L-Tryptophan 73-22-3 5.000
L-Tyrosine Disodium Salt 69847-45-6 28.830
L-Valine 72-18-4 20.000
Component CAS Number mg/L
VITAMINS
Choline chloride 67-48-1 3.000
D-Biotin 58-85-5 0.200
D-Ca-Pantothenate 137-08-6 0.250
Folic acid 59-30-3 1.000
Niacinamide 98-92-0 1.00
Pyridoxine hydrochloride 58-56-0 1.00
Riboflavin 83-88-5 0.200
Thiamine hydrochloride 67-03-8 1.000
Vitamin B12 68-19-9 0.005
p-Amino benzoic acid (PABA) 150-13-0 1.000
OTHERS
i-Inositol 87-89-8 35.000
D-Glucose 50-99-7 2000.000
Glutathione reduced 70-18-8 1.000
Phenol red sodium salt 34487-61-1 5.300
Custom formulation: Contact support@diagnocine.com for DCP-RPMI-QPB1X modifications.
Quality Assurance

Manufacturing & compliance

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

verified

ISO 13485:2016 Quality Management

Manufactured under an ISO 13485:2016-certified quality management system. Final QC at Diagnocine's R&D Center, Totowa, NJ, USA.

water_drop

Ultrapure Type 1 Water

18.2 MΩ·cm resistivity feedwater minimizes trace-metal and organic-carbon content in every batch.

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; a Certificate of Analysis is issued for every lot.

Endotoxin — USP <85> BET

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

Particulate — USP <788> Method 1

NMT 25/mL (≥10 µm), NMT 3/mL (≥25 µm) by light obscuration.

Osmolality — USP <785>

Target: 230–270 mOsm/kg H₂O.

Documentation & CoA

Full CoA with raw-material traceability available 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-RPMI-QPB1X compares

FluxMPS™ DCP-RPMI-QPB1X specifications set against published supplier data where available.

Parameter DCP-RPMI-QPB1X (FluxMPS™) Published Comparison
Grade Microfluidics Suitable Not specified
Formulation Triple-omission RPMI 1640 (no L-glutamine, no sodium pyruvate, no sodium bicarbonate) Not specified
Final filtration pore size 0.04 µm Not specified
Number of filtration stages 4 (Quadruple-stage) Not specified
Mycoplasma control 0.1 µm mycoplasma-retentive filtration (not tested per lot) Not specified
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 Tested, Method 1 (light obscuration) Not specified
Water quality Ultrapure Type 1, 18.2 MΩ·cm Not specified
Manufacturing QMS ISO 13485:2016 Not specified
Microfluidic channel compatible check_circle Yes Not specified
Custom formulation check_circle Available on request 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-RPMI-QPB1X — RPMI 1640.

Yes. DCP-RPMI-QPB1X is processed through a Quadruple-stage filtration system reaching a 0.04 µm final pore size, delivering ultra-low particulate counts for microphysiological system (MPS), organ-on-a-chip (OoC), and lab-on-a-chip (LoC) platforms. This RPMI 1640 formulation is suited to immune cell OoC, tumor-immune interaction chips, and lymphocyte perfusion models where standard 0.22 µm-filtered RPMI can introduce particulate-driven TLR4 activation artifacts.
FluxMPS™ uses four sequential filtration passes — 0.1 µm prefiltration I, 0.04 µm final filtration I, 0.1 µm prefiltration II, and 0.04 µm final filtration II (polish) — reaching a 0.04 µm final pore size versus the 0.22 µm typical of conventional media. This reduces particulate counts by approximately 5× and applies 0.1 µm mycoplasma-retentive filtration at each production run (not tested per lot).
This triple-omission formulation gives investigators full control over buffering and carbon/nitrogen metabolism: add fresh L-glutamine (or a stable dipeptide substitute), sodium pyruvate, and either sodium bicarbonate (for CO₂-buffered culture) or HEPES (for CO₂-independent culture) at the concentrations required by your assay. This is particularly useful for metabolic-flux studies in T cells, B cells, and lymphoma lines where defined nutrient control is essential.
No. This formulation is bicarbonate-free and CO₂-independent; supplement with 15–25 mM HEPES for pH buffering under atmospheric conditions, or add sodium bicarbonate if a CO₂ incubator will be used.
Yes. Fetal bovine serum, growth factors, cytokines, and other supplements can be added. Filter serum-containing or protein-containing additions through a 0.2 µm low-protein-binding PES or PVDF membrane before use; defined, protein-free additions may be filtered at 0.1 µm. Do not use a 0.04 µm membrane for supplement filtration — it retains immunoglobulins, lipoproteins, and much of the functional serum fraction. Contact support@diagnocine.com for custom co-formulation.
Every batch is tested by LAL assay (USP <85> Bacterial Endotoxins Test; assay sensitivity 0.005 EU/mL) and must meet a release specification of < 0.05 EU/mL before it ships. Endotoxin is controlled per manufacturing batch rather than per unit. For immune cell assays, keeping endotoxin low reduces the risk of TLR4/NF-κB-driven cytokine release and lymphocyte activation artifacts that can confound experimental readouts.
Yes. A CoA is available for every lot, covering appearance, pH (USP <791>), osmolality (USP <785>), sterility (USP <71>), endotoxin (USP <85>), mycoplasma control status, particulate count (USP <788> Method 1), and lot number and expiry. Request at support@diagnocine.com.
Scientific References

Supporting literature

Key publications supporting RPMI 1640 in immune cell culture and OoC applications.

  1. Moore GE, et al. Culture of normal human leukocytes. JAMA. 1967;199:519–524. doi:10.1001/jama.1967.03120080053007
  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. Ma C, et al. Organ-on-a-chip: a new paradigm for drug development. Trends Pharmacol Sci. 2021;42:119–133. doi:10.1016/j.tips.2020.11.009
  8. Sung JH, et al. Microfabricated mammalian organ systems. Lab Chip. 2013;13:1201–1212. doi:10.1039/c3lc41017j
  9. Junkin M, et al. High-content quantification of single-cell immune dynamics. Cell Rep. 2016;15:411–422. doi:10.1016/j.celrep.2016.03.033

Satisfaction
Quality Rating
Value Rating
Style Rating
X