Dulbecco’s PBS NP-40 Buffer [1X]

Product#: DCP-DPBSNP401X
$61.37
DCP-DPBSNP401X
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FluxMPS™ Buffer
ISO 13485 Certified Manufacturing

FluxMPS™ Dulbecco's PBS NP-40 Buffer [1X]

An MPS-grade, ultrapure lysis and extraction buffer that combines the osmotic balance and pH stability of Dulbecco's phosphate-buffered saline with the gentle membrane-permeabilization power of 1% NP-40 detergent. Dual-stage filtered through a 0.1 µm membrane once and a 0.04 µm membrane once for ultra-clean, microchannel-safe performance in cell lysis, fractionation, and immunostaining protocols.

  • Filtered 0.1 µm membrane once and 0.04 µm membrane once for ultra-clean, low-particulate buffer
  • Formulated with 1% NP-40 detergent for gentle, effective membrane protein extraction
  • Phosphate-buffered pH 7.4 for stable osmotic balance during lysis and downstream assays
  • Manufactured in ISO 13485-certified, CE-approved facilities
  • Supplied non-sterile, formulated for research bench lysis, fractionation, and immunostaining workflows
  • Compatible with centrifugal ultrafiltration for NP-40 removal and high-recovery protein purification
  • Customizable concentration, pH, and additive content available on request
SKU: DCP-DPBSNP401X UNSPSC 12161706 Neutral Buffers · Phosphate Buffer
Dulbecco's PBS NP-40 Buffer [1X] — Lysis & Extraction Buffer
  • pH7.4
  • Sodium Chloride137 mM
  • Potassium Chloride2.67 mM
  • Potassium Phosphate monobasic1.47 mM
  • Sodium Phosphate dibasic8.09 mM
  • NP-40 Detergent1%
  • AppearanceClear, Colorless Liquid
  • Filtration0.1 µm once + 0.04 µm once
  • Storage4°C
  • Shelf Life2 years
ISO 13485:2016 USP <85> <785> <788> RUO
Why FluxMPS™

Engineered where standard lysis buffers fall short

Conventional 0.22 µm-filtered PBS-NP-40 preparations can carry subvisible particulates that accumulate in microchannels, interfere with imaging, and introduce variability into protein extraction workflows. DCP-DPBSNP401X is built for cleaner, more reproducible lysis.

filter_alt

Microchannel-safe purity

Dual-stage 0.1 µm and 0.04 µm membrane filtration removes particulates that can clog microchannels and biosensor surfaces, keeping the buffer compatible with lysis and fractionation steps on- and off-chip.

target

Precise, stable pH

The phosphate buffer system holds pH 7.4, preserving protein structure and activity during NP-40-mediated membrane permeabilization and extraction.

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Ultrapure-grade water

Formulated with Ultrapure Type 1 water (18.2 MΩ·cm), reducing background contamination in sensitive downstream assays.

visibility

Low background for imaging & assays

Gentle NP-40 permeabilization supports immunostaining protocols that require intracellular antibody access without harsh membrane disruption.

science

Defined, traceable composition

Every salt and detergent component — from sodium chloride to NP-40 — is documented at a fixed concentration for reproducible lysis performance.

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Customization on demand

Concentration, pH, and additive content can be adjusted upon request for specialized extraction or fractionation protocols.

Purity Architecture

Dual-stage filtration system

DCP-DPBSNP401X is a non-sterile, ultrapure buffer filtered through a 0.1 µm membrane once and a 0.04 µm membrane once, removing coarse and fine particulates before fill.

  1. 1

    0.1 µm Pre-filtration I

    Removes large particulates and aggregates, extending the working life of the finer downstream membrane.

  2. 2

    0.04 µm Pre-filtration II

    Retains fine particulates and bioburden below the size of the smallest known mycoplasma types (about 0.2 µm), supporting an ultra-clean buffer for cell and molecular biology work.

Performance vs. conventional buffer

Sequential 0.1 µm and 0.04 µm filtration removes finer particulates than a single-pass 0.22 µm filtered buffer, supporting a cleaner working buffer for cell and molecular biology experiments.

0.04 µm
Final filtration stage
2
Total filtration stages
This product is supplied non-sterile for research use. Dual-stage 0.1 µm and 0.04 µm filtration reduces particulate and bioburden levels without constituting a sterility claim.
DCP-DPBSNP401X FluxMPS Dulbecco's PBS NP-40 buffer dual-stage 0.1 micron and 0.04 micron filtration diagram for organ-on-a-chip and microfluidic lysis applications, Diagnocine
Figure 1. Dual-stage 0.1 µm and 0.04 µm membrane filtration architecture used to produce DCP-DPBSNP401X.
© Diagnocine® — DCP-DPBSNP401X
Applications

Where DCP-DPBSNP401X performs

The addition of NP-40 to Dulbecco's PBS creates a versatile buffer that combines osmotic balance and pH stability with protein extraction and membrane permeabilization, valuable across a wide range of biological and biochemical workflows.

Automated Bioreactors & Robotics

Next-Generation System Uptime

For automated perfusion and robotic liquid-handling platforms, an optional 0.01 µm (10 nm) ultra-filtered variant of this buffer is available to further reduce particulate load on sensitive valves and sensors.

  • Total Particulate Exclusion for closed-loop perfusion systems
  • Valve & Sensor Protection in automated liquid-handling equipment
  • Extended Perfusion Stability for long-duration bioreactor runs

Inquiry Required: the 0.01 µm ultra-filtered grade is produced to order — contact support@diagnocine.com to request it.

Microfluidics

Micro Physiological System (MPS) & Chip Lysis

Ultra-clean NP-40 lysis buffer for on-chip cell disruption and protein extraction in microfluidic culture systems.

OoCToCBoCLoCMPS
Sample Preparation

Cell Lysis & Protein Extraction

NP-40 effectively lyses cells and solubilizes membrane proteins, preparing lysates for downstream biochemical assays.

LysisDilutionReconstitutionRinse
Stem Cell Biology

iPSC-Derived Model Lysate Preparation

Gentle detergent lysis supports protein recovery from iPSC-derived neuronal, cardiac, and hepatic models.

iPSC-NeuronsiPSC-CMiPSC-Hep
Vascular Biology

Endothelial & Primary Cell Fractionation

Used in protocols to separate nuclear and cytoplasmic fractions of endothelial and primary cell cultures.

HUVECsHAECsPrimary hepatocytes
Immunoassays

Immunostaining & Membrane Permeabilization

Permeabilizes cells to allow antibody access to intracellular targets in immunostaining protocols.

ELISAWestern blotIHCIF
Live-Cell Imaging

Nuclear/Cytoplasmic Fractionation Imaging

Low-background formulation supports downstream microscopy and biosensor readouts after fractionation.

ConfocalBiosensorsTEER
Technical Specifications

Specifications at a glance

Values reflect the DCP-DPBSNP401X formulation as documented by DiagnoCine Precision.

Physical & Chemical Parameters
Parameter Specification
Formulation / Composition Dulbecco's PBS with 1% NP-40 detergent — see full composition table below
Appearance Clear, Colorless Liquid
pH (USP <791>) 7.4
Sterility, Purity & Safety Parameters
Parameter Specification
Sterility (USP <71>) Non-sterile; filtered 0.1 µm membrane once and 0.04 µm membrane once
Water Purity USP <85> Ultrapure Type 1 water (18.2 MΩ·cm)
Manufacturing Standard ISO 13485 ISO 13485-certified, CE-approved facilities
Storage, Handling & Logistics
Parameter Specification
Storage Temperature 4°C
Shelf Life 2 years
Raw Materials & Regulatory Traceability
Parameter Specification
Manufacturing QMS ISO 13485 ISO 13485-certified facilities
Regulatory Alignment CE-approved supplier facilities
Production & Assembly Site Final packaging, QA, and testing at the DiagnoCine R&D and Quality Testing Center; customization and assembly at DiagnoCine Precision, Totowa, New Jersey, USA
Intended Use Research Use Only (RUO)
Formulation

Full composition

Every component and concentration of the DCP-DPBSNP401X formulation, as documented by DiagnoCine Precision.

Component CAS Number Concentration
Sodium Chloride 7647-14-5 137 mM
Potassium Chloride 7447-40-7 2.67 mM
Potassium Phosphate monobasic (KH2PO4) 7778-77-0 1.47 mM
Sodium Phosphate dibasic (Na2HPO4) 7558-79-4 8.09 mM
NP-40 Detergent 9036-19-5 1%
Custom concentrations, additional chemicals/compounds/proteins/supplements, alternate pH, and other modifications are available — contact support@diagnocine.com.
Quality Assurance

Manufacturing & compliance

DCP-DPBSNP401X is produced under a controlled quality management system with documented filtration, verification, and traceability practices.

verified

ISO 13485:2016 QMS

Manufactured under ISO 13485-certified and CE-approved supplier facilities.

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Ultrapure Type 1 Water

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

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Dual-Stage Membrane Filtration

Filtered 0.1 µm membrane once and 0.04 µm membrane once ahead of fill.

assignment

Micro-Batch Precision

Final packaging, QA, and testing are completed at the DiagnoCine R&D and Quality Testing Center; customization and assembly at DiagnoCine Precision, Totowa, New Jersey, USA.

pH Verification (USP <791>)

Formulated and verified to pH 7.4 using USP <791> potentiometric methodology.

Dual-Stage Membrane Filtration

Sequential 0.1 µm and 0.04 µm filtration, each applied once, prior to fill.

Water Quality

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

Documentation / CoA

A Certificate of Analysis is available upon request via support@diagnocine.com.

Contact support@diagnocine.com to request a Certificate of Analysis for a specific lot.
Product Comparison

How DCP-DPBSNP401X compares

A side-by-side look at filtration architecture and manufacturing practice versus conventional buffer options.

Parameter DCP-DPBSNP401X (FluxMPS™) Conventional 0.22 µm Filtered Buffer Standard Alternative (0.22 µm Filtered Buffer)
NP-40 detergent-based lysis + phosphate-buffered pH stability check_circle cancel cancel
Final filtration pore size 0.04 µm 0.22 µm 0.22 µm
Number of filtration stages 2 1 1
Water quality Ultrapure Type 1 (18.2 MΩ·cm) Standard purified water Standard purified water
Manufacturing QMS ISO 13485-certified, CE-approved Not specified Not specified
Microfluidic / microchannel compatibility check_circle cancel cancel
Documented, lot-defined pH 7.4 formulation check_circle cancel cancel
Custom formulation available check_circle cancel cancel
FAQ

Frequently asked questions

Answers to common questions about DCP-DPBSNP401X.

Yes. Its dual-stage 0.1 µm and 0.04 µm filtration produces an ultra-clean, low-particulate buffer suitable for lysis and fractionation steps within microfluidic and organ-on-a-chip workflows. It is supplied non-sterile for research bench use.
DCP-DPBSNP401X is filtered through a 0.1 µm membrane once and a 0.04 µm membrane once, retaining particulates and bioburden below the size of the smallest known mycoplasma types (about 0.2 µm), a finer cut than a single 0.22 µm pass.
The buffer is formulated at pH 7.4 with 137 mM Sodium Chloride, 2.67 mM Potassium Chloride, 1.47 mM Potassium Phosphate monobasic, 8.09 mM Sodium Phosphate dibasic, and 1% NP-40. Alternate concentrations and pH values can be produced on request via support@diagnocine.com.
pH 7.4 is the documented specification for this lot. Store at 4°C and allow the buffer to equilibrate before use in pH-sensitive assays.
Yes. Additional concentrations, chemicals, compounds, proteins, supplements, alternate pH, and other modifications can be arranged — contact support@diagnocine.com to discuss your protocol.
DCP-DPBSNP401X is a non-sterile research buffer and does not carry a routine endotoxin specification. For applications requiring endotoxin data, contact support@diagnocine.com to discuss custom testing options.
Yes. A CoA covering appearance, pH, and the filtration process is available upon request via support@diagnocine.com.
Scientific References

Supporting literature

Curated literature relevant to phosphate-buffered saline chemistry, NP-40 lysis, and buffer use in microfluidic and organ-on-a-chip systems.

  1. Bhatia SN, Ingber DE. Microfluidic organs-on-chips. Nat Biotechnol. 2014. doi:10.1038/nbt.2989
  2. Huh D, et al. Reconstituting organ-level lung functions on a chip. Science. 2010. doi:10.1126/science.1188302
  3. Ganesan A, et al. Comparison of lysis buffers for extraction of membrane proteins from mammalian cells. J Proteome Res. 2011. doi:10.1021/pr200070h
  4. Seddon AM, Curnow P, Booth PJ. Membrane proteins, lipids and detergents: not just a soap opera. Biochim Biophys Acta. 2004. doi:10.1016/j.bbamem.2004.04.011
  5. Good NE, et al. Hydrogen ion buffers for biological research. Biochemistry. 1966. doi:10.1021/bi00866a011
  6. Suarez-Arnedo A, et al. An image-based method to quantify cell permeabilization efficiency. PLoS One. 2020. doi:10.1371/journal.pone.0232565
  7. Low LA, Tagle DA. Microphysiological systems (organs-on-chips) for drug efficacy and toxicity testing. Clin Transl Sci. 2017. doi:10.1111/cts.12444
  8. Ho C-T, et al. Liver-cell patterning lab chip: mimicking the morphology of liver lobule tissue. Lab Chip. 2013. doi:10.1039/C3LC50402F
  9. Rathnasinghe R, et al. Sample preparation methods for downstream immunoassay applications. Methods Mol Biol. 2018. doi:10.1007/978-1-4939-7883-0

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