FluxMPS™ RPMI 1640 Medium, High Glucose:1X Liquid

Product#: DCP-RPMIWOHB1X
$49.50
DCP-RPMIWOHB1X
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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™ RPMI 1640 Medium, High Glucose — 1X Liquid

Contains L-Glutamine Contains Sodium Bicarbonate Contains Phenol Red Contains Calcium Contains Magnesium Contains High Glucose Contains Sodium Pyruvate

Microfluidics Suitable, quadruple-stage ultra-filtered (0.1 µm ×2 + 0.04 µm ×2) RPMI 1640 High Glucose formulation engineered for hematopoietic cells, lymphocytes, and related immune cell models on organ-on-a-chip (OoC) and microphysiological system (MPS) platforms. The quadruple-stage train reaches a 0.04 µm final cut-off — five times finer than the 0.22 µm membranes used in conventional sterile filtration. Formulation: [+] High Glucose (4500 mg/L), [+] L-Glutamine, [+] Sodium Pyruvate, [+] Sodium Bicarbonate, [+] Phenol Red.

  • High Glucose formulation: 4500 mg/L (4.5 g/L) D-glucose to support elevated glycolytic demand in activated lymphocytes and Warburg-active cancer lines
  • L-Glutamine (300 mg/L) and Sodium Pyruvate (110 mg/L) included as standard nitrogen and carbon sources
  • Glutathione (reduced, 1.0 mg/L) — antioxidant support for redox-sensitive lymphocyte and hematopoietic cell types
  • Sodium bicarbonate–buffered (2000 mg/L NaHCO₃); formulated for 5% CO₂ incubation
  • Quadruple-stage filtration (0.1 µm ×2 + 0.04 µm ×2) reaching a 0.04 µm final cut-off — Microfluidics Suitable
  • Endotoxin release specification < 0.05 EU/mL (LAL assay, USP <85>)
  • Manufactured under an ISO 13485:2016 quality management system; final QC at Diagnocine, Totowa, NJ
  • Contains phenol red sodium salt (5.3 mg/L) as a pH indicator
CAT. NO.
DCP-RPMIWOHB1X | Cell Culture Media UNSPSC: 41116155 | Commodity: Molecular biology and cell culture growth media | (UNv260801)
RPMI 1640 High Glucose — 1X Liquid
  • Glucose4500 mg/L (4.5 g/L, High Glucose)
  • L-Glutamine300 mg/L
  • Sodium Pyruvate110 mg/L
  • pH (USP <791>)7.4
  • Osmolality (USP <785>)280–320 mOsm/kg H₂O
  • Endotoxin (USP <85>)< 0.05 EU/mL
  • Filtration0.1 µm ×2 + 0.04 µm ×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 RPMI passes mycoplasma-sized organisms and subvisible particulates that accumulate in microchannel geometries and confound immune cell assays. FluxMPS™ is built to a finer standard.

filter_alt

Microchannel-safe purity

0.04 µm final filtration with USP <788> Method 1 (light obscuration) particulate compliance — suited to suspension immune cell OoC and flow cytometry workflows.

target

Complete metabolic profile

High Glucose (4500 mg/L), L-Glutamine (300 mg/L), and Sodium Pyruvate (110 mg/L) are all present as standard, supporting a full range of glycolytic and oxidative metabolic assays.

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Ultrapure-grade water

Formulated with Type 1 water (18.2 MΩ·cm) — low trace-metal and organic-carbon (TOC) background supports consistent formulation quality lot to lot.

visibility

Low background for imaging

Quadruple-stage filtration reduces particulate baseline relative to 0.22 µm media, supporting confocal microscopy and biosensor readouts where subvisible particulates raise background signal. Contains phenol red; not recommended for red/PE-channel fluorescence work.

science

Rich, stable nutrient profile

RPMI 1640’s balanced amino acid and vitamin profile, plus reduced glutathione (1.0 mg/L), supports demanding lymphocyte, hematopoietic, and cancer cell line culture.

tune

Customization on demand

pH, glucose concentration, salts, HEPES, and nutrient composition available on request — contact support@diagnocine.com.

Purity Architecture

Quadruple-stage filtration system

Four serial filtration stages — two dedicated 0.1 µm/0.04 µm prefilter-and-final-filter pairs in series — reach a validated 0.04 µm final pore size. Each 0.04 µm final filter is protected by its own dedicated 0.1 µm prefilter, giving full redundancy across the train.

  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 mycoplasma-sized organisms (0.2–0.3 µm) and sub-micron particulates that pass a standard 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 in a validated ISO Class 5 (Class 100) environment.

Purity architecture vs. conventional media

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.

5.5×
Finer pore size than standard 0.22 µm filtration (0.22 ÷ 0.04)
4
Validated filtration passes prior to aseptic fill
Sterility & Mycoplasma: No growth after 14-day incubation (USP <71>). Mycoplasma risk is mitigated by 0.1 µm mycoplasma-retentive filtration; this is a filtration control, not a per-lot mycoplasma assay.
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 RPMI 1640 High Glucose DCP-RPMIWOHB1X quadruple-stage filtration system, 0.1 micron x2 plus 0.04 micron x2, for organ-on-a-chip and microfluidic cell culture applications, Diagnocine
Figure 1. FluxMPS™ Quadruple-stage filtration system (0.1 µm ×2 + 0.04 µm ×2).
© Diagnocine® — DCP-RPMIWOHB1X
Applications

Immune cell OoC and hematopoietic applications

FluxMPS™ DCP-RPMIWOHB1X — RPMI 1640 High Glucose — delivers 0.04 µm filtered purity for hematopoietic cells, lymphocytes, and related OoC applications.

Automated Bioreactors & Robotics

Next-Generation System Uptime

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

  • 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.

Immunology

T Cell & Lymphocyte Culture

RPMI 1640 is the standard formulation for primary T cells, B cells, NK cells, and monocytes. Quadruple-stage 0.04 µm filtration reduces particulate load relevant to immune assay consistency.

T cellsB cellsNK cellsPBMC
Cancer Biology

Leukemia & Lymphoma Lines

RPMI supports NCI-60 cancer lines, Jurkat, Raji, K562, HL-60, and hematopoietic cancer lines broadly, where the High Glucose formulation supports elevated glycolytic demand.

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 within microphysiological systems (MPS).

Tumor-immune chipLymph node OoCMPS
Immunotherapy

CAR-T & TIL Expansion

Endotoxin release specification <0.05 EU/mL supports CAR-T manufacturing and TIL expansion protocols sensitive to endotoxin-driven activation artefacts.

CAR-TTILTCR-T
Metabolomics

Immune Cell Metabolic Flux

Defined RPMI base for glycolysis stress tests and ¹³C isotope tracing of lymphocyte activation states. Not compatible with Agilent Seahorse XF assays, which require bicarbonate-free, phenol red-free medium.

¹³C tracingGlycolysis
Live-Cell Imaging

Flow Cytometry & Confocal

Reduced particulate baseline supports confocal imaging and flow cytometry workflows. Contains phenol red; low-autofluorescence variants available on request for red/PE-channel work.

Flow cytometryConfocalELISA
Technical Specifications

Analytical release specifications

Every lot released against the full specification matrix. CoA: support@diagnocine.com. Available in 500 mL and 1000 mL pack sizes.

Physical & Chemical Parameters
Parameter Specification
Formulation [+] L-Glutamine (300 mg/L), [+] Sodium Bicarbonate (2000 mg/L), [+] Phenol Red (5.3 mg/L), [+] Calcium, [+] Magnesium, [+] High Glucose (4500 mg/L), [+] Sodium Pyruvate (110 mg/L)
Appearance Red-colored, clear solution
Glucose 4500 mg/L (4.5 g/L, High Glucose)
pH USP <791> 7.4
Osmolality USP <785> 280–320 mOsm/kg H₂O
Total ingredients 41 components across 4 category groups
Sterility, Purity & Safety Parameters
Parameter Specification
Endotoxin USP <85> BET < 0.05 EU/mL (batch release — see §Manufacturing)
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, 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 5% CO₂ required (sodium bicarbonate-buffered, 2000 mg/L NaHCO₃)
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 High Glucose: 41 ingredients verified per lot with CAS numbers for full raw-material traceability. Contains reduced glutathione and a balanced profile of vitamins and amino acids for 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 bicarbonate 144-55-8 2000.000
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-Glutamine 56-85-9 300.000
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 1.000
Pyridoxine hydrochloride 58-56-0 1.000
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 4500.000
Glutathione reduced 70-18-8 1.000
Phenol red sodium salt 34487-61-1 5.300
Sodium Pyruvate 113-24-6 110.000
Custom formulation: Contact support@diagnocine.com for DCP-RPMIWOHB1X 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 quality management system. Final QC at Diagnocine R&D Center, Totowa, NJ, USA.

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Ultrapure Type 1 Water

18.2 MΩ·cm feed water supports low trace-metal and organic-carbon background in the finished medium.

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.

Endotoxin — USP <85> BET

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

Particulate — USP <788> Method 1

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

Osmolality — USP <785>

Target: 280–320 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-RPMIWOHB1X compares

FluxMPS™ DCP-RPMIWOHB1X vs. conventional 0.22 µm–filtered RPMI formulations.

Parameter DCP-RPMIWOHB1X (FluxMPS™) Conventional RPMI 1640 High Glucose (0.22 µm filtered) Standard alternative (0.22 µm filtered)
Grade Microfluidics Suitable Not applicable Not applicable
RPMI 1640 High Glucose (4.5 g/L) — for Warburg-active cancer lines and activated T cells 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 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 (Method 1) cancel No cancel No
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 Yes cancel Risk of clogging cancel Risk of clogging
Custom formulation check_circle On request cancel No cancel No

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-RPMIWOHB1X — RPMI 1640 High Glucose.

Yes. DCP-RPMIWOHB1X is processed through a quadruple-stage filtration system reaching a 0.04 µm final pore size — a Microfluidics Suitable grade — suited to immune cell OoC, tumor-immune interaction chips, and lymphocyte perfusion models on MPS platforms.
FluxMPS™ uses four sequential filters — 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 cut-off, five times finer than the 0.22 µm membranes used in conventional sterile filtration.
High Glucose RPMI (4.5 g/L) supports rapidly proliferating cancer cell lines with elevated glycolytic demand (Warburg effect), certain T-cell activation protocols, and hematopoietic models where glucose consumption exceeds the standard 2 g/L supply. L-Glutamine (300 mg/L), Sodium Pyruvate (110 mg/L), and reduced glutathione are already included; additional supplementation is generally not required.
Yes. This formulation is sodium bicarbonate–buffered (2000 mg/L NaHCO₃) and requires a 5% CO₂ incubator to maintain the target pH of 7.4.
Yes. Add FBS (5–10%), serum-free supplements, or growth factors as required. Filter serum-containing or protein-containing additions through a 0.2 µm low-protein-binding PES or PVDF membrane before adding to the medium — never through a 0.04 µm membrane, which retains IgM, lipoproteins, and much of the functional serum fraction. Contact support@diagnocine.com for custom co-formulation.
DCP-RPMIWOHB1X is released to meet < 0.05 EU/mL by LAL assay (USP <85>), controlled per manufacturing batch. Elevated endotoxin can activate TLR4/NF-κB signaling in immune cells, inducing cytokine release and altering lymphocyte activation state independent of experimental treatment.
Yes. A full CoA is available per batch, covering appearance, pH (USP <791>), osmolality (USP <785>), sterility (USP <71>), endotoxin (USP <85>), mycoplasma filtration status, particulate count (USP <788> Method 1), and raw-material traceability. Request at support@diagnocine.com.
Scientific References

Supporting literature

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

  1. Moore GE, et al. Culture of normal human leukocytes. JAMA. 1967;199:519–524. doi:10.1083/jcb.1.3.273
  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. Rock KL, Kono H. The inflammatory response to cell death. Annu Rev Pathol. 2008;3:99–126. doi:10.1146/annurev.pathmechdis.3.121806.151456
  8. Sung JH, et al. Microfabricated mammalian organ systems. Lab Chip. 2013;13:1201–1212. doi:10.1039/c3lc41017j

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