FluxMPS™ RPMI 1640 Medium w/o Phenol Red: 1X Liquid

Product#: DCP-RPMI-R1X
$34.10
DCP-RPMI-R1X
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FluxMPS™ RPMI 1640

FluxMPS™ DCP-RPMI-R1X is an MPS-grade, ultra-filtered RPMI 1640 formulation engineered for Hematopoietic cells and related cell models on organ-on-a-chip (OoC) and microphysiological system (MPS) platforms. Processed through a Quadruple-stage filtration system (0.1 µm ×2 + 0.04 µm ×2), it delivers approximately 5× lower particulate counts than conventional 0.22 µm–filtered media. Formulation: [+] 2 g/L Glucose, [+] L-Glutamine, [+] Sodium Pyruvate, [+] Sodium Bicarbonate | [-] Phenol Red.

  • Glucose source: 2000 mg/L (2.0 g/L)
  • Glutathione (reduced) included — antioxidant support for redox-sensitive cell types
  • 0.04 µm final nano-filtration — sub-mycoplasma purity; < 0.05 EU/mL endotoxin
  • Quadruple-stage filtration: 0.1 µm pre-I → 0.04 µm pre-II → 0.1 µm sterile-I → 0.04 µm final polish
  • Ultrapure Type 1 water (18.2 MΩ·cm), ISO 13485:2016 QMS, ISO Class 5 fill
CAT. NO.
DCP-RPMI-R1X | UNSPSC 41122100 Cell Culture Media
RPMI 1640 — 1X Liquid
  • Media familyRPMI 1640
  • Glucose2000 mg/L (2.0 g/L)
  • Formulation[+] 2 g/L Glucose, [+] L-Glutamine, [+] Sodium Pyruvate, [+] Sodium Bicarbonate, [-] Phenol Red
  • AppearanceOrange-colored, clear solution
  • pH (USP <791>)7.4
  • Osmolality (USP <785>)280.00–320.00 mOsm/kg H₂O
  • Endotoxin (USP <85>)< 0.05 EU/mL
  • Filtration0.1 µm ×2 + 0.04 µm ×2
  • Shelf Life12 months / 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, subvisible particulates, and endotoxin fragments that activate TLR4 and confound immune cell assays. FluxMPS™ eliminates these failure modes.

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Microchannel-safe purity

0.04 µm final filtration; USP <788> particulate compliance. Particle-free media for suspension immune cell OoC and flow cytometry.

science

Immune cell–optimized formulation

RPMI 1640 contains glutathione (antioxidant) and a balanced profile of vitamins and amino acids optimized for lymphocyte and hematopoietic cell culture.

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Ultrapure-grade water

18.2 MΩ·cm — eliminates ionic contaminants that alter lymphocyte signaling thresholds.

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Below TLR4 endotoxin threshold

< 0.05 EU/mL — prevents LPS-driven T cell and NK cell activation artefacts in immune assays.

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Rich nutrient profile

RPMI contains specialized nutrients for demanding cell types — delivered particle-free for OoC use.

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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 reaching a final 0.04 µm polish under ISO Class 5 aseptic conditions.

  1. 1

    0.1 µm Pre-filtration I — Large Particulate Removal

    Removes large aggregates; protects downstream 0.04 µm membranes.

  2. 2

    0.04 µm Pre-filtration II — Mycoplasma Barrier

    Retains mycoplasma (0.1–0.3 µm) — absent from standard 0.22 µm filtration.

  3. 3

    0.1 µm Sterile-filtration I — Second-pass Redundancy

    Second-pass sterility redundancy; no breakthrough from Stage 1.

  4. 4

    0.04 µm Sterile-filtration II — Final Polish

    Ultimate sub-mycoplasma polish; ISO Class 5 aseptic fill & finish.

Performance vs. conventional media

FluxMPS™ DCP-RPMI-R1X delivers approximately 5× lower particulate counts than standard 0.22 µm filtered RPMI, with confirmed mycoplasma barrier at every production stage.

Cleaner than 0.22 µm media by particulate count
0.04
µm Final pore size — sub-mycoplasma polishing
Sterility & Mycoplasma: No growth after 14-day incubation (USP <71>); mycoplasma-negative by 0.04 µm barrier every lot.
FluxMPS-Quadruple-stage-filtration-system-Cell-Culture-Media-Diagnocine-V2.jpg
Figure 1. FluxMPS™ Quadruple-stage filtration system (0.1 µm ×2 + 0.04 µm ×2).
© Diagnocine® — DCP-RPMI-R1X
Applications

Immune cell OoC and hematopoietic applications

FluxMPS™ DCP-RPMI-R1X — RPMI 1640 — delivers 0.04 µm filtered purity for Hematopoietic cells and related OoC applications.

Automated Bioreactors & Robotics

Next-Generation System Uptime

Optional 0.01 µm (10 nm) ultra-filtered variant available on request.

  • Total Particulate Exclusion: 10 nm filtration removes nanoparticulate aggregates
  • Valve & Sensor Protection: Eliminates micro-fouling 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 variant.

Immunology

T Cell & Lymphocyte Culture

RPMI 1640 is the standard for primary T cells, B cells, NK cells, and monocytes. FluxMPS 0.04 µm filtration prevents particulate TLR4 activation that confounds immune assays.

T cellsB cellsNK cellsPBMC
Cancer Biology

Leukemia & Lymphoma Lines

RPMI supports NCI-60 cancer lines, Jurkat, Raji, K562, HL-60, and all hematopoietic cancer lines where DMEM 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 where particle-free media prevents TLR4 activation.

Tumor-immune chipLymph node OoCMPS
Immunotherapy

CAR-T & TIL Expansion

Ultra-low endotoxin (<0.05 EU/mL) prevents LPS-driven T cell activation artefacts in CAR-T manufacturing and TIL expansion protocols.

CAR-TTILTCR-T
Metabolomics

Immune Cell Metabolic Flux

Defined RPMI base for Seahorse XF T cell metabolic assays, glycolysis stress tests, and ¹³C isotope tracing of lymphocyte activation states.

Seahorse XF¹³C tracingGlycolysis
Live-Cell Imaging

Flow Cytometry & Confocal

Ultra-low particulate; phenol red–free variants eliminate autofluorescence for PE-channel flow cytometry and immune cell confocal imaging.

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 [+] 2 g/L Glucose, [+] L-Glutamine, [+] Sodium Pyruvate, [+] Sodium Bicarbonate | [-] Phenol Red
Appearance Orange-colored, clear solution
Glucose 2000 mg/L (2.0 g/L)
pH USP <791> 7.4
Osmolality USP <785> 280.00–320.00 mOsm/kg H₂O
Total ingredients 40
Sterility, Purity & Safety
Parameter Specification
Endotoxin USP <85> BET < 0.05 EU/mL
Sterility USP <71> No growth / 14 days
Mycoplasma Negative (0.04 µm barrier)
Particulate ≥10 µm USP <788> NMT 25/mL
Particulate ≥25 µm USP <788> 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 manufacture
Shipping condition cold pack
CO₂ requirement 5% CO₂ required (sodium bicarbonate buffering)
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
Regulatory alignment 21 CFR Part 820 (cGMP) aligned
Production method Micro-batch, per-lot QC release
Intended use Research Use Only (RUO)
Formulation

Full composition (mg/L)

RPMI 1640: 40 ingredients verified per lot with CAS numbers for full raw-material traceability. RPMI 1640 contains glutathione (antioxidant) and a balanced profile of vitamins and amino acids optimized for lymphocyte and hematopoietic cell culture.

Component CAS Number mg/L
INORGANIC SALTS
Calcium nitrate tetrahydrate 13477-34-4 100.000
Magnesium sulphate 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 6000.00
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
i-Inositol 87-89-8 35.000
p-Amino benzoic acid (PABA) 150-13-0 1.000
OTHERS
D-Glucose 50-99-7 2000.000
Glutathione reduced 70-18-8 1.000
Sodium Pyruvate 113-24-6 110.000
Custom formulation: Contact support@diagnocine.com for DCP-RPMI-R1X modifications.
Quality Assurance

Manufacturing & compliance

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

verified

ISO 13485:2016 Quality Management

Manufactured under ISO 13485:2016–certified and CE-approved facilities. Final QA at DiagnoCine R&D Center, Totowa, NJ, USA.

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Ultrapure Type 1 Water

18.2 MΩ·cm — eliminates ionic contaminants.

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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 for every lot.

Endotoxin — USP <85> BET

LAL assay < 0.05 EU/mL per lot.

Particulate — USP <788> Method 2

≤25/mL (≥10 µm), ≤3/mL (≥25 µm).

Osmolality — USP <785>

Target: 280.00–320.00 mOsm/kg H₂O.

Documentation & CoA

Full CoA with raw-material traceability available on request.

Certificate of Analysis: Request for any DCP-RPMI-R1X lot at support@diagnocine.com.
Product Comparison

How DCP-RPMI-R1X compares

FluxMPS™ DCP-RPMI-R1X vs. conventional 0.22 µm–filtered RPMI formulations.

Parameter DCP-RPMI-R1X (FluxMPS™) Conventional RPMI 1640
(0.22 µm filtered)
Standard DMEM/RPMI
(0.22 µm filtered)
RPMI 1640 without Phenol Red — autofluorescence-free for flow cytometry, confocal, and hormone-sensitive assays 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 barrier check_circle Yes (0.04 µm) cancel No cancel No
Endotoxin specification < 0.05 EU/mL NMT 1 EU/mL NMT 1 EU/mL
USP <788> particulate tested check_circle Yes 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 compatible check_circle MPS-grade cancel Risk of clogging cancel Risk of clogging
FAQ

Frequently asked questions

Common questions about FluxMPS™ DCP-RPMI-R1X — RPMI 1640.

DCP-RPMI-R1X is processed through a Quadruple-stage filtration system reaching 0.04 µm final pore size. RPMI 1640 with sub-mycoplasma filtration purity is suited to immune cell OoC, tumor-immune interaction chips, and lymphocyte perfusion models where standard RPMI would cause particulate TLR4 activation.
FluxMPS™ uses four sequential filters — 0.1 µm pre-filtration I, 0.04 µm pre-filtration II (mycoplasma barrier), 0.1 µm sterile-filtration I, and 0.04 µm final polish — resulting in approximately 5× fewer particles and confirmed mycoplasma retention at every production stage.
Phenol red is removed to eliminate autofluorescence at 520–560 nm and its weak estrogenic activity. Essential for lymphocyte flow cytometry (PE channel interference), immune cell confocal imaging, hormone-sensitive cancer cell assays (ER+ breast cancer, endocrine tumors), and any ELISA-based assay where phenol red absorbs at relevant wavelengths.
5% CO₂ required (sodium bicarbonate buffering).
Yes. Add FBS (5–10%), serum-free supplements, growth factors, or antibiotics as required. Contact support@diagnocine.com for custom co-formulation.
FluxMPS™ DCP-RPMI-R1X is produced to meet < 0.05 EU/mL by LAL assay (USP <85>). For immune cells, endotoxin above 0.1 EU/mL activates TLR4/NF-κB, inducing cytokines and altering lymphocyte activation state independently of experimental conditions.
Yes. Full CoA per lot covers: appearance, pH (USP <791>), osmolality (USP <785>), sterility (USP <71>), endotoxin (USP <85>), mycoplasma, particulate count (USP <788> Method 2), and raw-material traceability. 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:10.1083/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. 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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