Tyrode's Balanced Salts Solution w/ Sodium bicarbonate and Phenol red: 1X

Product#: DCP-TBSSBR1X
$71.50
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FluxMPS™ Buffer
ISO 13485 Certified Manufacturing

FluxMPS™ Tyrode's Balanced Salts Solution w/ Sodium Bicarbonate and Phenol Red: 1X

An MPS-grade, physiologically balanced isotonic salt solution formulated with a sodium bicarbonate buffering system and a phenol red visual pH indicator. Quadruple-stage filtered through 0.1 µm membrane twice and 0.04 µm membrane twice, this ready-to-use buffer delivers ultra-low particulate purity suited to microfluidic channels, organ-on-a-chip perfusion, and precise physiological pH monitoring.

  • Quadruple-stage filtration: 0.1 µm membrane twice and 0.04 µm membrane twice for ultra-low particulate purity
  • Endotoxin content NMT 1 EU/mL
  • Target pH 7.4, maintained by a sodium bicarbonate buffering system
  • Osmolality 270.00 - 310.00 mOsm/Kg H2O, isotonic with interstitial fluid
  • Phenol Red included for immediate visual pH monitoring
  • Sterile; no bacterial or fungal growth after 14 days incubation per USP specification
  • pH, molarity, and additive customization available on request — contact support@diagnocine.com
SKU: DCP-TBSSBR1X · 12161706 - Neutral Buffers · Balanced Salt Solutions
Tyrode's Balanced Salts Solution w/ Sodium Bicarbonate & Phenol Red, 500 mL
  • pH7.4
  • Osmolality270.00 - 310.00 mOsm/Kg H2O
  • Buffer SystemSodium Bicarbonate
  • pH IndicatorPhenol Red
  • EndotoxinNMT 1 EU/mL
  • SterilityUSP 14-Day, No Growth
  • Filtration0.1 µm x2 + 0.04 µm x2
  • AppearanceColorless, Clear Solution
  • Storage4°C, Protect from Light
  • Shelf Life24 Months
ISO 13485:2016 USP <85> <785> <788> RUO
Why FluxMPS™

Engineered where standard buffers fail

Conventional 0.22 µm-filtered balanced salt solutions can carry subvisible particulates that accumulate in narrow microchannels, drift in pH and ionic balance, and introduce assay background. Tyrode's Balanced Salts Solution is manufactured to a tighter purity standard purpose-built for sensitive cell, tissue, and microfluidic work.

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Microchannel-safe purity

Quadruple-stage filtration through 0.1 µm and 0.04 µm membranes reduces particulate load beyond a single 0.22 µm pass, protecting narrow microfluidic and organ-on-a-chip channels.

target

Precise, stable pH

A sodium bicarbonate buffering system holds the solution at pH 7.4, with phenol red providing an immediate visual cue for pH status during use.

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Ultrapure-grade water

Formulated with Ultrapure Type 1 water (18.2 MΩ·cm), minimizing trace contaminants that can interfere with sensitive cell and tissue assays.

visibility

Low background for imaging & assays

A colorless, clear base solution with a built-in phenol red indicator supports clean visual and optical readouts during physiological experiments.

science

Defined, traceable composition

Every inorganic salt and additive is manufactured and released to a defined mg/L specification, supporting reproducible ionic composition across lots.

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Customization on demand

Alternate concentrations, additional chemicals, compounds, proteins, supplements, or pH modifications are available — contact support@diagnocine.com.

Purity Architecture

Quadruple-stage filtration system

This buffer is filter-sterilized through a 0.1 µm membrane twice and a 0.04 µm membrane twice, providing sequential pre-filtration and sterile-filtration passes that go beyond a single 0.22 µm sterilizing-grade pass.

  1. 1

    0.1 µm Pre-filtration I

    Removes large particulates and aggregates from the formulated solution, extending the working life of the downstream filters.

  2. 2

    0.04 µm Pre-filtration II

    Retains fine particulates and bioburden ahead of the final sterile-filtration passes, an important step given that the smallest mycoplasma types can be about 0.2 microns.

  3. 3

    0.1 µm Sterile-filtration I

    A second 0.1 µm pass provides redundant particulate and bioburden reduction ahead of final polishing.

  4. 4

    0.04 µm Sterile-filtration II — Final Polish

    A second 0.04 µm pass under ISO Class 5 (Class 100) aseptic fill conditions delivers the final purity polish before packaging.

Performance vs. conventional buffer

Sequential 0.1 µm and 0.04 µm filtration removes finer particulates than a single 0.22 µm pass typical of conventional balanced salt solutions, supporting the world's cleanest buffer standard for cell and molecular biology work.

0.04 µm
Final filtration stage
4
Total filtration stages
Sterility is verified per USP specification, with no bacterial or fungal growth observed after 14 days of incubation. This filtration architecture is intended to help prevent mycoplasma contamination.
DCP-TBSSBR1X FluxMPS Tyrode's Balanced Salts Solution quadruple-stage 0.1 micron and 0.04 micron filtration diagram for organ-on-a-chip and microfluidic buffer applications, Diagnocine
Figure 1. Quadruple-stage filtration architecture: 0.1 µm membrane filtration twice and 0.04 µm membrane filtration twice.
© Diagnocine® — DCP-TBSSBR1X
Applications

Where Tyrode's Balanced Salts Solution is used

Physiologically balanced and isotonic with interstitial fluid, this solution supports cell and tissue culture maintenance, isolated organ perfusion, and physiological experiments requiring precise pH monitoring.

Automated Bioreactors & Robotics

Next-Generation System Uptime

An optional 0.01 µm (10 nm) ultra-filtered variant is available for automated bioreactor and robotic liquid-handling platforms where valve and sensor protection is critical.

  • Total Particulate Exclusion for automated fluidics
  • Valve & Sensor Protection in robotic dispensing systems
  • Extended Perfusion Stability in closed-loop bioreactors

Inquiry Required: Contact support@diagnocine.com to request the 0.01 µm ultra-filtered grade.

Microfluidics

Micro Physiological System (MPS) & Chip

Supports isolated organ perfusion studies and electrophysiological recordings in cardiac and smooth muscle tissue within microfluidic formats.

OoCToCBoCLoCMPS
Sample Preparation

Wash, Dilution & Reconstitution

Used for washing of cells and tissues during experimental procedures and short-term preservation of isolated tissues and organs.

LysisDilutionReconstitutionRinse
Stem Cell Biology

iPSC-Derived Model Handling

Provides an isotonic, buffered environment for cell and tissue culture maintenance of sensitive stem cell-derived models.

iPSC-NeuronsiPSC-CMiPSC-Hep
Vascular Biology

Endothelial & Primary Cell Perfusion

Supports isolated organ perfusion studies and physiological experiments in cardiac and smooth muscle tissue models.

HUVECsHAECsPrimary hepatocytes
Immunoassays

ELISA, Blotting & Blocking

Its low-particulate, defined ionic background suits use as a wash or dilution buffer in immunoassay workflows.

ELISAWestern blotIHCIF
Live-Cell Imaging

Microscopy & Optical Sensing

The colorless, clear formulation with a phenol red pH indicator supports physiological experiments requiring precise pH monitoring during imaging.

ConfocalBiosensorsTEER
Technical Specifications

Product specifications

Values below are drawn directly from this product's release specification.

Physical & Chemical Parameters
Parameter Specification
Formulation / Composition Balanced salt solution with sodium bicarbonate and phenol red
Appearance Colorless, clear solution
pH USP <791> 7.4
Osmolality USP <785> 270.00 - 310.00 mOsm/Kg H2O
Sterility, Purity & Safety Parameters
Parameter Specification
Endotoxin USP <85> NMT 1 EU/mL
Sterility USP <71> No bacterial or fungal growth after 14 days of incubation
Toxicity Test Passes
Water Quality Ultrapure Type 1 water (18.2 MΩ·cm)
Manufacturing Standard ISO 13485-certified, CE-approved facilities
Fill Environment ISO Class 5 (Class 100)
Storage, Handling & Logistics
Parameter Specification
Storage Temperature 4°C, away from bright light
Shelf Life 24 months
Expiry Use before expiry date given on the product label
Raw Materials & Regulatory Traceability
Parameter Specification
Manufacturing Facility ISO 13485-certified and CE-approved facilities (DiagnoCine Precision suppliers)
Traceability Final packaging, quality assurance, and testing at the DiagnoCine R&D and Quality Testing Center
Manufacturing QMS ISO 13485:2016
Regulatory Alignment CE-approved
Production Method Customization and assembly at DiagnoCine Precision, Totowa, New Jersey, USA
Intended Use Research Use Only (RUO)
Formulation

Full composition

Component concentrations are expressed in mg/L, as manufactured and released for this lot-controlled formulation.

Component CAS Number Concentration (mg/L)
Calcium chloride dihydrate (CaCl2·2H2O) 10035-04-8 265.000
Magnesium chloride anhydrous (MgCl2) 7786-30-3 46.900
Potassium chloride (KCl) 7447-40-7 200.000
Sodium bicarbonate (NaHCO3) 144-55-8 1000.000
Sodium chloride (NaCl) 7647-14-5 8000.000
Sodium dihydrogen phosphate anhydrous (NaH2PO4) 7558-80-7 50.000
Component CAS Number Concentration (mg/L)
D-Glucose (C6H12O6) 50-99-7 1000.000
Phenol Red (C19H14O5S) 143-74-8 15.000
Alternate concentrations, additions of chemicals, compounds, proteins, supplements, different pH, and other modifications are available on request — contact support@diagnocine.com.
Quality Assurance

Manufacturing & compliance

Every lot is manufactured, filled, and released under a controlled quality system.

verified

ISO 13485:2016 QMS

Manufactured under ISO 13485-certified and CE-approved facilities (suppliers of DiagnoCine Precision).

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Ultrapure Type 1 Water

Formulated with Ultrapure Type 1 water (18.2 MΩ·cm) as the base for consistent ionic quality.

biotech

ISO Class 5 Fill & Finish

Final sterile-filtration and fill occur under ISO Class 5 (Class 100) conditions.

assignment

Micro-Batch Precision

Final packaging, quality assurance, and testing are completed at the DiagnoCine R&D and Quality Testing Center.

Endotoxin USP <85> BET

Specification: NMT 1 EU/mL.

Particulate USP <788> Method 2

Filtration is performed in line with USP <788> Method 2 particulate-control practices.

Osmolality USP <785>

Specification: 270.00 - 310.00 mOsm/Kg H2O.

Documentation / CoA

A Certificate of Analysis is available for this lot — contact support@diagnocine.com.

Certificates of Analysis (CoA) for this product are available on request at support@diagnocine.com.
Product Comparison

How DCP-TBSSBR1X compares

A side-by-side look at filtration architecture and quality attributes against conventional buffered saline solutions.

Parameter DCP-TBSSBR1X (FluxMPS™) Conventional Buffer (0.22 µm filtered) Standard Alternative (0.22 µm filtered)
Bicarbonate-buffered, phenol red indicated check_circle cancel cancel
Final filtration pore size 0.04 µm 0.22 µm 0.22 µm
Number of filtration stages 4 1 1
Endotoxin specification NMT 1 EU/mL cancel cancel
USP <788> particulate compliance check_circle cancel cancel
Ultrapure Type 1 water base check_circle cancel cancel
Manufacturing QMS ISO 13485:2016 cancel cancel
Microfluidic channel compatibility check_circle cancel cancel
Visual pH indicator included check_circle cancel cancel
Custom formulation available check_circle cancel cancel
FAQ

Frequently asked questions

Answers to the most common questions about DCP-TBSSBR1X.

Yes. Its quadruple-stage filtration (0.1 µm membrane twice and 0.04 µm membrane twice) and physiologically balanced, isotonic formulation make it suitable for microfluidic and organ-on-a-chip perfusion, isolated organ perfusion studies, and electrophysiological recordings in cardiac and smooth muscle tissue.
This buffer is filter-sterilized using a 0.1 µm filtration step twice and a 0.04 µm filtration step twice, providing sequential particulate and bioburden removal beyond a single 0.22 µm pass. This architecture is intended to help prevent mycoplasma contamination, since the smallest mycoplasma types can be about 0.2 microns.
The solution is formulated to pH 7.4 with an osmolality of 270.00 - 310.00 mOsm/Kg H2O, buffered by sodium bicarbonate. Alternate concentrations, additional compounds, or pH modifications can be requested at support@diagnocine.com.
The listed pH of 7.4 reflects the formulation as manufactured; a specific measurement temperature is not designated in the product specification. Store the solution at 4°C away from bright light and allow it to equilibrate to your intended working conditions before use.
Yes. DiagnoCine can formulate customized versions with additional chemicals, compounds, proteins, or supplements on request — contact support@diagnocine.com to discuss your protocol.
The specification is NMT 1 EU/mL. Sterility is confirmed per USP specification, with no bacterial or fungal growth observed after 14 days of incubation, and the solution passes toxicity testing.
Yes. A lot-specific Certificate of Analysis is available on request at support@diagnocine.com, reflecting the release testing performed at the DiagnoCine R&D and Quality Testing Center.
Scientific References

Supporting literature

Curated literature relevant to balanced salt solutions, bicarbonate buffering, and microphysiological system applications.

  1. Bhatia SN, Ingber DE. Microfluidic organs-on-chips. Nat Biotechnol. 2014;32(8):760-772. doi:10.1038/nbt.2989
  2. Huh D, Matthews BD, Mammoto A, et al. Reconstituting organ-level lung functions on a chip. Science. 2010;328(5986):1662-1668. doi:10.1126/science.1188302
  3. Low LA, Mummery C, Berridge BR, et al. Organs-on-chips: into the next decade. Nat Rev Drug Discov. 2021;20(5):345-361. doi:10.1038/s41573-020-0079-3
  4. Ronaldson-Bouchard K, Vunjak-Novakovic G. Organs-on-a-chip: a fast track for engineered human tissues in drug development. Cell Stem Cell. 2018;22(3):310-324. doi:10.1016/j.stem.2018.02.011
  5. Good NE, Winget GD, Winter W, et al. Hydrogen ion buffers for biological research. Biochemistry. 1966;5(2):467-477. doi:10.1021/bi00866a011
  6. Halldorsson S, Lucumi E, Gomez-Sjoberg R, Fleming RMT. Advantages and challenges of microfluidic cell culture in polydimethylsiloxane devices. Biosens Bioelectron. 2015;63:218-231. doi:10.1016/j.bios.2014.07.029
  7. Sung JH, Wang YI, Narasimhan Sriram N, et al. Microfabricated mammalian organ systems and their integration into models of whole animals and humans. Lab Chip. 2013;13(7):1201-1212. doi:10.1039/c3lc41017j
  8. Hasiwa N, Daneshian M, Bruegger P, et al. Evidence for the detection of non-endotoxin pyrogens by the whole blood monocyte activation test. ALTEX. 2013;30(2):169-208. doi:10.14573/altex.2013.2.169
  9. Esch EW, Bahinski A, Huh D. Organs-on-chips at the frontiers of drug discovery. Nat Rev Drug Discov. 2015;14(4):248-260. doi:10.1038/nrd4539

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