Hank's Balanced Salt Solution with Ca2+, Mg2+ and 20 mM HEPES without Phenol Red

Product#: DCP-HBSSH-R1X
$55.00
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Neutral Buffer · Balanced Salt Solution
ISO 13485 Certified Manufacturing

FluxMPS™ Hank's Balanced Salt Solution with Ca2+, Mg2+ and 20 mM HEPES without Phenol Red

An MPS-grade physiological buffer formulated with calcium, magnesium, and a 20 mM HEPES buffering system to maintain a precise, stable pH of 7.4 across cell culture, microfluidic, and organ-on-a-chip (OoC) workflows. Quadruple-stage filtered for microchannel-safe purity, this phenol-red-free solution supports cell-to-cell adhesion, membrane integrity, and low-background imaging.

  • Quadruple-stage filtration — 0.1 µm membrane twice and 0.04 µm membrane twice — for microchannel-safe, ultra-low-particulate purity
  • Contains Ca2+ and Mg2+ to preserve cell-to-cell adhesion, signaling, and membrane integrity
  • Buffered with 20 mM HEPES for stable pH 7.4 (25°C) throughout handling
  • Osmolality isotonic with body fluids for proper osmotic equilibrium
  • Phenol-red free — compatible with fluorescence, luminescence, and imaging-based assays
  • DNase- and RNase-tested: none detected after 18 hr incubation at room temperature
  • pH, molarity, tracking dyes, and other modifications available on request — contact support@diagnocine.com
Cat. No. DCP-HBSSH-R1X · UNSPSC 12161706 Balanced Salt Solutions
Hank's Balanced Salt Solution with Ca2+, Mg2+ & 20 mM HEPES (No Phenol Red)
  • pH7.4 (25°C)
  • FormulationHBSS + Ca2+/Mg2+ + 20 mM HEPES
  • Buffering AgentHEPES, 20 mM
  • OsmolalityIsotonic with body fluids
  • Filtration0.1 µm ×2 + 0.04 µm ×2
  • SterilityFiltered in a sterile environment
  • DNase ActivityNone detected
  • RNase ActivityNone detected
  • Storage4°C
  • Shelf Life2 years
ISO 13485:2016 USP <85> <785> <788> RUO
Why FluxMPS™

Engineered where standard buffers fail

Conventional single-pass 0.22 µm-filtered buffers can carry subvisible particulates that accumulate in narrow microchannels, drift in pH and ionic balance during handling, and introduce background into sensitive imaging or biosensing assays. FluxMPS™ buffers are engineered specifically to remove these failure modes.

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Microchannel-safe purity

Quadruple-stage filtration down to a 0.04 µm final pore size reduces particulate load relevant to USP <788> testing, protecting narrow microfluidic channels and valves.

target

Precise, stable pH

A defined 20 mM HEPES buffering system holds pH at 7.4 (25°C), supporting reproducible cellular behavior across wash, transport, and dilution steps.

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Ultrapure-grade water

Formulated with ultrapure Type 1 water (18.2 MΩ·cm), consistent with USP <85> expectations for biological buffer preparation.

visibility

Low background for imaging & assays

Phenol-red free formulation minimizes optical interference in fluorescence, luminescence, and live-cell imaging applications.

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Defined, traceable composition

Every inorganic salt, sugar, and buffering agent is formulated to a stated concentration and documented for lot traceability.

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Customization on demand

pH, concentration, tracking dye additions, and other modifications are available — contact support@diagnocine.com.

Purity Architecture

Quadruple-stage filtration system

This buffer is sterile-filtered through a 0.1-micron membrane twice and a 0.04-micron membrane twice, delivering the world's cleanest buffer purity level for cell and molecular biology experiments.

  1. 1

    0.1 µm Pre-filtration I

    Removes large particulates and aggregates, extending the life of downstream filters.

  2. 2

    0.04 µm Pre-filtration II

    Retains fine particulates and bioburden, including organisms well below the mycoplasma size range.

  3. 3

    0.1 µm Sterile-filtration I

    A second independent 0.1 µm pass adds redundancy to the sterilization process.

  4. 4

    0.04 µm Sterile-filtration II — Final Polish

    The final 0.04 µm polish is performed under aseptic fill conditions ahead of packaging.

Performance vs. conventional buffer

Sequential 0.1 µm and 0.04 µm filtration passes remove finer particulates than a single conventional 0.22 µm filtration used in standard buffers, supporting cleaner microchannels and reduced particulate interference in sensitive assays.

0.04 µm
Final filtration stage
4
Total filtration stages
All FluxMPS™ Precision Sterile buffers are filtered-sterilized with 0.1-micron filtration twice and 0.04-micron filtration twice, helping prevent mycoplasma contamination; the smallest mycoplasma species measure approximately 0.2 micron.
DCP-HBSSH-R1X FluxMPS quadruple-stage filtration diagram showing 0.1 micron membrane twice and 0.04 micron membrane twice for HBSS buffer used in organ-on-a-chip and microfluidic applications, Diagnocine
Figure 1. Quadruple-stage filtration architecture (0.1 µm membrane twice, 0.04 µm membrane twice) applied to DCP-HBSSH-R1X.
© Diagnocine® — DCP-HBSSH-R1X
Applications

Where this buffer is used

A versatile, physiological buffer suited to cell washing, short-term maintenance, transport, and reagent preparation across cell and molecular biology workflows, including microfluidic and organ-on-a-chip systems.

Automated Bioreactors & Robotics

Next-Generation System Uptime

For automated perfusion systems and robotic liquid handling, an optional 0.01 µm (10 nm) ultra-filtered variant of this buffer can be requested to further protect sensitive valves and sensors.

  • Total Particulate Exclusion — minimizes subvisible particulate entering closed-loop perfusion systems
  • Valve & Sensor Protection — reduces the risk of fouling in automated microvalves and inline sensors
  • Extended Perfusion Stability — supports longer unattended run times in bioreactor and OoC platforms

Inquiry Required: the 0.01 µm ultra-filtered grade is available upon request — contact support@diagnocine.com.

Microfluidics

Micro Physiological System (MPS) & Chip

Supports perfusion and wash steps in microfluidic tissue-chip platforms.

OoCToCBoCLoCMPS
Sample Preparation

Wash, Dilution & Reconstitution

Used to rinse cells before dissociation and to dilute cell suspensions for accurate counting.

LysisDilutionReconstitutionRinse
Stem Cell Biology

iPSC-Derived Model Handling

Calcium and magnesium content supports adhesion-dependent iPSC-derived cell models.

iPSC-NeuronsiPSC-CMiPSC-Hep
Vascular Biology

Endothelial & Primary Cell Perfusion

Isotonic, Ca2+/Mg2+-containing formulation suited to primary and endothelial cell perfusion.

HUVECsHAECsPrimary hepatocytes
Immunoassays

ELISA, Blotting & Blocking

Serves as a base wash/dilution buffer supporting immunoassay workflows.

ELISAWestern blotIHCIF
Live-Cell Imaging

Microscopy & Optical Sensing

Phenol-red free formulation reduces optical background during live-cell imaging.

ConfocalBiosensorsTEER
Technical Specifications

Detailed specifications

Physical, chemical, purity, and handling parameters for DCP-HBSSH-R1X.

Physical & Chemical Parameters
Parameter Specification
Formulation HBSS with Ca2+, Mg2+ and 20 mM HEPES, without phenol red
Appearance Clear solution
pH (USP <791>) USP <791> 7.4 (25°C)
Osmolality (USP <785>) USP <785> Isotonic with body fluids
Buffering agent HEPES, 20 mM
Sterility, Purity & Safety Parameters
Parameter Specification
Sterility Filtered 0.1-micron membrane twice and 0.04-micron membrane twice in a sterile environment
DNase activity None detected (plasmid DNA, 18 hr, room temperature)
RNase activity None detected (ribosomal RNA, 18 hr, room temperature)
Water quality Ultrapure Type 1 water, 18.2 MΩ·cm
Manufacturing standard ISO 13485:2016 certified; CE-approved facility
Storage, Handling & Logistics
Parameter Specification
Storage temperature 4°C
Shelf life 2 years
Raw Materials & Regulatory Traceability
Parameter Specification
Manufacturing QMS ISO 13485:2016 certified, CE-approved facility (Suppliers of DiagnoCine Precision)
Traceability Final packaging, QA, and testing performed at the DiagnoCine R&D and Quality Testing Center
Production & customization site DiagnoCine Precision, Totowa, New Jersey, USA
Intended use Research Use Only (RUO)
Formulation

Full composition

Every inorganic salt, sugar, and buffering agent in DCP-HBSSH-R1X, formulated to the stated concentration.

Component CAS Number Concentration
Sodium Chloride (NaCl) 7647-14-5 137.93 mM
Potassium Chloride (KCl) 7447-40-7 5.33 mM
Calcium Chloride (CaCl2) 10043-52-4 1.26 mM
Magnesium Sulfate (MgSO4) 7487-88-9 0.41 mM
Magnesium Chloride (MgCl2) 7786-30-3 0.49 mM
Sodium Phosphate Dibasic (Na2HPO4) 7558-79-4 0.338 mM
Potassium Phosphate Monobasic (KH2PO4) 7778-77-0 0.44 mM
Sodium Bicarbonate (NaHCO3) 144-55-8 4.17 mM
D-Glucose (Dextrose) 50-99-7 5.56 mM
HEPES 7365-45-9 20 mM
Need a different formulation? Other concentrations, tracking dye additions, alternate pH, and other modifications are available on request — contact support@diagnocine.com.
Quality Assurance

Manufacturing & compliance

DCP-HBSSH-R1X is manufactured under ISO 13485-certified and CE-approved facilities, with final packaging, quality assurance, and testing performed at the DiagnoCine R&D and Quality Testing Center.

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ISO 13485:2016 QMS

Manufactured under an ISO 13485-certified, CE-approved quality management system.

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Ultrapure Type 1 Water

Formulated with ultrapure Type 1 water (18.2 MΩ·cm).

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Sterile Fill & Finish

Quadruple-stage filtered and sterile-filled prior to packaging.

assignment

Micro-Batch Precision

Specific customization requests and assembly are completed at DiagnoCine Precision in Totowa, New Jersey, USA.

DNase & RNase Testing

None detected after incubation of plasmid DNA or ribosomal RNA with this product for 18 hr at room temperature.

Sterility

Filtered with a 0.1-micron membrane twice and a 0.04-micron membrane twice in a sterile environment.

Osmolality (USP <785>)

Isotonic with body fluids, maintaining osmotic equilibrium for cultured cells.

Documentation

A Certificate of Analysis is available on request.

Request a Certificate of Analysis for this lot at support@diagnocine.com.
Product Comparison

How DCP-HBSSH-R1X compares

A side-by-side look at filtration architecture and quality practices versus conventional 0.22 µm-filtered buffers.

Parameter DCP-HBSSH-R1X (FluxMPS™) Conventional Buffer Standard Alternative
Buffering system (HEPES, pH 7.4) check_circle cancel cancel
Final filtration pore size 0.04 µm 0.22 µm 0.22 µm
Number of filtration stages 4 1 1
DNase/RNase tested check_circle cancel cancel
Ultrapure Type 1 water check_circle cancel cancel
ISO 13485:2016 manufacturing check_circle cancel cancel
Microfluidic/OoC channel compatibility check_circle cancel cancel
Custom formulation available check_circle cancel cancel
FAQ

Frequently asked questions

Common questions about DCP-HBSSH-R1X.

Yes. The buffer is quadruple-stage filtered (0.1-micron membrane twice, 0.04-micron membrane twice) to reduce particulate load relevant to narrow microfluidic channels and organ-on-a-chip devices.
Sequential 0.1-micron and 0.04-micron filtration passes remove finer particulates than a single conventional 0.22-micron pass, supporting cleaner microchannels and reduced assay interference.
The buffer is formulated to pH 7.4 (25°C) with the salt and HEPES concentrations shown in the composition table above. Other concentrations, pH values, and modifications are available on request.
pH is specified as 7.4 at 25°C. The product should be stored at 4°C, with a shelf life of 2 years from manufacture.
Yes. Other concentrations, additions of tracking dyes, different pH, and other modifications can be requested by contacting support@diagnocine.com.
Endotoxin testing is not reported on the standard specification sheet for this lot; a Certificate of Analysis with full lot-specific testing detail is available on request.
Yes. A CoA is available on request and includes appearance, pH, sterility/filtration, and DNase/RNase testing results. Contact support@diagnocine.com.
Scientific References

Supporting literature

Curated references on HEPES buffering chemistry and organ-on-a-chip / microfluidic applications.

  1. Good NE, Winget GD, Winter W, Connolly TN, Izawa S, Singh RM. Hydrogen ion buffers for biological research. Biochemistry. 1966;5(2):467-477. doi:10.1021/bi00866a011
  2. Bhatia SN, Ingber DE. Microfluidic organs-on-chips. Nat Biotechnol. 2014;32(8):760-772. doi:10.1038/nbt.2989
  3. Huh D, Hamilton GA, Ingber DE. From 3D cell culture to organs-on-chips. Trends Cell Biol. 2011;21(12):745-754. doi:10.1016/j.tcb.2011.09.005
  4. Low LA, Mummery C, Berridge BR, Austin CP, Tagle DA. Organs-on-chips: into the next decade. Nat Rev Drug Discov. 2021;20(5):345-361. doi:10.1038/s41573-020-0079-3
  5. Ingber DE. Human organs-on-chips for disease modeling, drug development and personalized medicine. Nat Rev Genet. 2022;23(8):467-491. doi:10.1038/s41576-022-00466-9
  6. Zhang B, Radisic M. Organ-on-a-chip devices advance to market. Lab Chip. 2017;17(14):2395-2420. doi:10.1039/C6LC01554A
  7. Sung JH, Wang YI, Narasimhan Sriram N, et al. Recent advances in body-on-a-chip systems. Anal Chem. 2019;91(1):330-351. doi:10.1021/acs.analchem.9b02593
  8. Freshney RI. Physiological buffered salt solutions in animal cell culture. Culture of Animal Cells: A Manual of Basic Technique and Specialized Applications. doi:10.1002/9781118873686

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