FluxMPS™ RPMI 1640 Medium with 25mM HEPES w/o L-Glutamine, Sodium Bicarbonate: 1X Liquid

Product#: DCP-RPMIH-QB1X
$44.00
DCP-RPMIH-QB1X
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verified ISO 13485 Certified Manufacturing

FluxMPS™ RPMI 1640

FluxMPS™ DCP-RPMIH-QB1X is an MPS-grade, ultra-filtered RPMI 1640 + 25mM HEPES 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. HEPES (25 mM, pKa 7.3 at 37°C) provides robust pH buffering. Formulation: [+] 2.0 g/L Glucose, [+] Sodium Pyruvate, [+] 25mM HEPES | [-] L-Glutamine, [-] Sodium Bicarbonate.

  • Glucose source: 2000 mg/L (2.0 g/L)
  • 25 mM HEPES (pKa 7.3 at 37°C) — robust pH buffering independent of CO₂
  • 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-RPMIH-QB1X | UNSPSC 41122100 Cell Culture Media
RPMI 1640 — 1X Liquid
  • Media familyRPMI 1640 + 25mM HEPES
  • Glucose2000 mg/L (2.0 g/L)
  • HEPES25 mM, pKa 7.3 at 37°C
  • Formulation[+] 2.0 g/L Glucose, [+] Sodium Pyruvate, [+] 25mM HEPES | [-] L-Glutamine, [-] Sodium Bicarbonate
  • AppearanceOrange-colored, clear solution
  • pH (USP <791>)7.4
  • Osmolality (USP <785>)230.00–270.00 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.

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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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HEPES pH stability

HEPES (25 mM) prevents pH rise during open-air handling, flow cytometry preparation, and atmospheric incubation.

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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-RPMIH-QB1X 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-RPMIH-QB1X
Applications

Immune cell OoC and hematopoietic applications

FluxMPS™ DCP-RPMIH-QB1X — RPMI 1640 + 25mM HEPES — 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 [+] 2.0 g/L Glucose, [+] Sodium Pyruvate, [+] 25mM HEPES | [-] L-Glutamine, [-] Sodium Bicarbonate
Appearance Orange-colored, clear solution
Glucose 2000 mg/L (2.0 g/L)
HEPES 25 mM (pKa 7.3 at 37°C)
pH USP <791> 7.4
Osmolality USP <785> 230.00–270.00 mOsm/kg H₂O
Total ingredients 39
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 CO₂-independent — 25 mM HEPES alone maintains pH 7.2–7.4 at 37°C
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 + 25mM HEPES: 39 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 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
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
HEPES 7365-45-9 5958.00
Phenol red sodium salt 34487-61-1 5.300
Sodium pyruvate 113-24-6 110.000
Custom formulation: Contact support@diagnocine.com for DCP-RPMIH-QB1X 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.

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 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: 230.00–270.00 mOsm/kg H₂O.

Documentation & CoA

Full CoA with raw-material traceability available on request.

Certificate of Analysis: Request for any DCP-RPMIH-QB1X lot at support@diagnocine.com.
Product Comparison

How DCP-RPMIH-QB1X compares

FluxMPS™ DCP-RPMIH-QB1X vs. conventional 0.22 µm–filtered RPMI formulations.

Parameter DCP-RPMIH-QB1X (FluxMPS™) Conventional RPMI 1640 + 25m
(0.22 µm filtered)
Standard DMEM/RPMI
(0.22 µm filtered)
RPMI 1640 + HEPES-only CO₂-free — fresh glutamine for atmospheric immune cell suspension 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
HEPES (25 mM) check_circle Yes cancel Usually 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-RPMIH-QB1X — RPMI 1640 + 25mM HEPES.

DCP-RPMIH-QB1X 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.
HEPES-only CO₂-independent; L-glutamine added fresh (2 mM). Ideal for atmospheric immune cell suspension cultures requiring precise nitrogen control.
CO₂-independent — 25 mM HEPES alone maintains pH 7.2–7.4 at 37°C.
Yes. Add FBS (5–10%), serum-free supplements, growth factors, or antibiotics as required. Contact support@diagnocine.com for custom co-formulation.
FluxMPS™ DCP-RPMIH-QB1X 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 + 25mM HEPES 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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