4% PFA with 1% Glutaraldehyde

Product#: DCP-PFAGA1X
$77.00
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Fixative Buffers
ISO 13485 Certified Manufacturing

FluxMPS™ 4% PFA with 1% Glutaraldehyde Fixative Buffer

DCP-PFAGA1X is an MPS-grade, dual-aldehyde fixative buffer combining 4% paraformaldehyde with 1% glutaraldehyde in 0.1M phosphate buffer at pH 7.4 for rapid tissue penetration paired with superior ultrastructural preservation. Sequentially filtered through 0.1 µm and 0.04 µm membranes and manufactured under ISO 13485-certified, CE-approved facilities, this methanol-free, ready-to-use formulation is suited to electron microscopy, immunohistochemistry, developmental biology, and organ-on-a-chip (OoC) tissue-model fixation.

  • Non-sterile, ultrapure, sequentially filtered through a 0.1 µm membrane once and a 0.04 µm membrane once
  • Dual-aldehyde formulation: 4% paraformaldehyde plus 1% glutaraldehyde
  • Prepared in 0.1M phosphate buffer at pH 7.4 for physiological compatibility
  • Methanol-free — eliminates membrane permeabilization artifacts of methanol-stabilized formalin
  • Ready-to-use, pre-mixed format for consistent results
  • Manufactured under ISO 13485-certified, CE-approved facilities
  • Custom concentrations, additives, and pH available on request
SKU: DCP-PFAGA1X UNSPSC: 12161703 · Other buffers Fixative Buffers
4% PFA with 1% Glutaraldehyde Fixative Buffer — 500 mL
  • pH7.4
  • Formulation4% PFA / 1% Glutaraldehyde
  • Buffer System0.1M Phosphate Buffer
  • Filtration0.1 µm once + 0.04 µm once
  • SterilityNon-Sterile
  • AppearanceClear solution
  • Storage4°C, protected from light
  • Shelf Life6 months
  • ShippingTypically within 48 hours (up to 1 week)
  • Size500 mL
ISO 13485:2016 USP <85> <785> <788> RUO
Why FluxMPS™

Engineered where standard fixatives fall short

Single-aldehyde formalin and unfiltered fixative solutions carry subvisible particulates, inconsistent aldehyde ratios, and variable pH that compromise ultrastructure and antigen accessibility. DCP-PFAGA1X is formulated and filtered to remove these failure modes.

filter_alt

Microchannel-safe purity

Sequential 0.1 µm and 0.04 µm membrane filtration reduces particulate load for clean fixation of tissue models in confined channels.

target

Precise, stable pH

Prepared in 0.1M phosphate buffer at pH 7.4 to maintain osmotic balance and minimize cellular distortion during fixation.

water_drop

Ultrapure-grade water

Formulated with ultrapure Type 1 water (18.2 MΩ·cm) to minimize trace contaminants that can interfere with downstream staining.

visibility

Low background for imaging & assays

Compatible with fluorescent proteins such as hyperfolder YFP, retaining approximately 70% initial fluorescence intensity compared with methanol-free 4% PFA alone.

science

Defined, traceable composition

A controlled, methanol-free dual-aldehyde formulation containing paraformaldehyde and glutaraldehyde in a fixed phosphate buffer background.

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Customization on demand

Other concentrations, additions of chemicals, compounds, proteins, or supplements, different pH, and formulation modifications are available on inquiry.

Purity Architecture

Dual-stage filtration system

DCP-PFAGA1X is filtered through a 0.1 µm membrane once and a 0.04 µm membrane once, reducing particulate load beyond a conventional single-pass filtration step while the fixative remains non-sterile as formulated.

  1. 1

    0.1 µm Pre-filtration I

    Large particulate and aggregate removal, extending the service life of downstream filtration.

  2. 2

    0.04 µm Pre-filtration II

    Fine particulate retention for a cleaner finished fixative solution.

Performance vs. conventional buffer

A sequential 0.1 µm and 0.04 µm filtration pass removes finer particulates than a single conventional filtration step, supporting cleaner backgrounds for downstream imaging and staining without altering the fixative chemistry.

0.04 µm
Final filtration stage
2
Total filtration stages
This fixative undergoes sequential 0.1 µm and 0.04 µm membrane filtration for particulate control; the finished product is supplied non-sterile as formulated for standard tissue fixation workflows.
DCP-PFAGA1X FluxMPS dual-stage 0.1 micron and 0.04 micron filtration diagram for PFA-glutaraldehyde fixative buffer used in organ-on-a-chip and microfluidic tissue fixation applications, Diagnocine
Figure 1. Dual-stage 0.1 µm and 0.04 µm filtration architecture applied to DCP-PFAGA1X.
© Diagnocine® — DCP-PFAGA1X
Applications

Where DCP-PFAGA1X is used

A balanced dual-aldehyde ratio makes this fixative suited to workflows that demand both rapid tissue stabilization and preserved ultrastructure, antigenicity, and fluorescence.

Automated Bioreactors & Robotics

Next-Generation System Uptime

An optional 0.01 µm (10 nm) ultra-filtered variant is available on inquiry for automated tissue processors and robotic liquid-handling platforms used in high-throughput histology and imaging workflows.

  • Total Particulate Exclusion for particulate-sensitive automated staining lines
  • Valve & Sensor Protection in robotic liquid-handling systems
  • Extended Stability during automated, unattended processing runs

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

Microfluidics

Organ-on-Chip & MPS Tissue Fixation

In-situ dual-aldehyde fixation of tissue models within microfluidic channels prior to imaging or immunostaining.

OoCToCBoCLoCMPS
Electron Microscopy

Ultrastructural Preservation for EM

The 1% glutaraldehyde concentration provides sufficient cross-linking for membrane preservation without excessive hardening, facilitating easier sectioning after osmium tetroxide staining.

TEMSEMUltrastructure
Fluorescence Imaging

Fluorescent Protein & Live-Cell Marker Preservation

Compatible with fluorescent proteins like hyperfolder YFP, retaining approximately 70% initial fluorescence intensity compared with methanol-free 4% PFA alone; retained fluorescence demonstrated for mitochondrial markers like MitoTracker Red.

hfYFPConfocalMitoTracker
Developmental Biology

Whole-Embryo & Craniofacial Tissue Fixation

Validated for embryonic tissue fixation, showing 23% less craniofacial distortion versus Karnovsky’s original 5% glutaraldehyde formula.

EmbryoCraniofacialWhole-mount
Immunoassays

IHC & IF Sample Preparation

Lower glutaraldehyde content preserves epitope accessibility, enabling reliable immunohistochemistry and immunofluorescence without extensive antigen retrieval steps.

IHCIFAntigen Retrieval
Sample Preparation

Standard Histology & Cytology Fixation

Ready-to-use, pre-mixed format ensures consistency and reduces preparation time compared with traditional ampoule-based fixation kits.

HistologyCytologyTissue Processing
Technical Specifications

Product parameters

All parameters below reflect DCP-PFAGA1X as formulated, filtered, and released by Diagnocine.

Physical & Chemical Parameters
Parameter Specification
Formulation 4% PFA + 1% Glutaraldehyde
Buffer System 0.1M Phosphate Buffer
Appearance Clear solution
pH USP <791> 7.4
Paraformaldehyde Penetration Rate 1–2 mm/hour
Sterility, Purity & Safety Parameters
Parameter Specification
Sterility Non-Sterile
Filtration 0.1 µm membrane once + 0.04 µm membrane once
Water Quality Ultrapure Type 1 water (18.2 MΩ·cm)
Manufacturing Standard ISO 13485 ISO 13485:2016-certified facility
Storage, Handling & Logistics
Parameter Specification
Storage Temperature 4°C, protected from light (amber)
Shelf Life 6 months
Shipping Condition Typically within 48 hours; up to 1 week during unforeseen events
Fixation Immersion Time 4–24 hours at 4°C
Rinse Protocol 3x with PBS or buffer
Raw Materials & Regulatory Traceability
Parameter Specification
Raw Material / Facility Grade ISO 13485-certified, CE-approved supplier facilities
Manufacturing QMS ISO 13485:2016
Regulatory Alignment CE-approved
Production & QA Location DiagnoCine R&D and Quality Testing Center, Totowa, New Jersey, USA
Intended Use Research Use Only (RUO)
Formulation

Full composition

Dual-aldehyde fixative composition, prepared in 0.1M phosphate buffer.

Component CAS Number Concentration
Paraformaldehyde (PFA) 30525-89-4 4%
Glutaraldehyde 111-30-8 1%
Phosphate Buffer   0.1M
Please inquire if other concentrations, additions of chemicals, compounds, proteins, or supplements, a different pH, or other formulation modifications are needed — contact support@diagnocine.com.
Quality Assurance

Manufacturing & compliance

DCP-PFAGA1X is manufactured under ISO 13485-certified and CE-approved facilities, with final packaging, quality assurance, and testing completed at the DiagnoCine R&D and Quality Testing Center.

verified

ISO 13485:2016 QMS

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

water_drop

Ultrapure Type 1 Water

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

biotech

Sequential Membrane Filtration

0.1 µm membrane filtration once and 0.04 µm membrane filtration once for particulate control.

assignment

Micro-Batch Traceability

Final packaging, QA, and testing performed at the DiagnoCine R&D and Quality Testing Center, Totowa, New Jersey, USA.

pH Verification USP <791>

Each lot is verified to a pH of 7.4.

Appearance QC

Each lot is verified as a clear solution.

Sterility Status

Non-Sterile; sequentially filtered through a 0.1 µm membrane once and a 0.04 µm membrane once.

Documentation / CoA

A Certificate of Analysis is available on request.

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

How DCP-PFAGA1X compares

A qualitative comparison against conventional and standard-alternative fixative solutions.

Parameter DCP-PFAGA1X (FluxMPS™) Conventional Fixative (Unfiltered) Standard Alternative (0.22 µm Filtered)
Dual-aldehyde formulation (4% PFA + 1% GA) check_circle cancel cancel
Final filtration pore size 0.04 µm Unfiltered 0.22 µm
Number of filtration stages 2 0 1
Methanol-free formulation check_circle cancel check_circle
Physiological phosphate buffering (0.1M, pH 7.4) check_circle cancel check_circle
ISO 13485 manufacturing QMS check_circle cancel cancel
Fluorescent protein compatibility check_circle cancel cancel
Custom formulation available check_circle cancel cancel
FAQ

Frequently asked questions

Common questions about DCP-PFAGA1X.

Yes. The methanol-free, dual-aldehyde formulation supports in-situ fixation of tissue models within microfluidic channels while preserving ultrastructure for downstream imaging or immunostaining.
DCP-PFAGA1X passes sequentially through a 0.1 µm membrane once and a 0.04 µm membrane once, removing finer particulates than a single 0.22 µm pass without altering the fixative chemistry.
DCP-PFAGA1X is prepared in 0.1M phosphate buffer at pH 7.4. Other concentrations, additions of chemicals, compounds, proteins, or supplements, and different pH values are available on inquiry to support@diagnocine.com.
The pH of 7.4 is a release specification for the formulation. Store at 4°C away from bright light (amber) to maintain stability through the 6-month shelf life and use before the expiry date on the product label.
Yes. Please inquire if other concentrations, additions of chemicals, compounds, proteins, or supplements, different pH, or other modifications are needed.
Endotoxin testing is not part of the standard release specification for this fixative formulation. Quality control includes appearance, pH, and sterility status — DCP-PFAGA1X is released as Non-Sterile, filtered through a 0.1 µm membrane once and a 0.04 µm membrane once.
Yes. A CoA covering appearance, pH, and sterility/filtration status is available on request at support@diagnocine.com.
Scientific References

Supporting literature

Curated literature relevant to dual-aldehyde fixation chemistry and its research applications.

  1. Karnovsky MJ. A formaldehyde-glutaraldehyde fixative of high osmolality for use in electron microscopy. J Cell Biol. 1965. doi:10.1083/jcb.27.2.137A
  2. Hopwood D. Fixatives and fixation: a review. Histochem J. 1969. doi:10.1007/BF01003278
  3. Hayat MA. Principles and Techniques of Electron Microscopy: Biological Applications. Cambridge University Press. doi:10.1017/CBO9780511605377
  4. Kiernan JA. Formaldehyde, formalin, paraformaldehyde and glutaraldehyde: what they are and what they do. Microsc Today. 2000. doi:10.1017/S1551929500057060
  5. Melan MA, Sluder G. Redistribution and differential extraction of soluble proteins in permeabilized cultured cells. J Cell Sci. 1992. doi:10.1242/jcs.101.4.731
  6. Schnell U, Dijk F, Sjollema KA, Giepmans BN. Immunolabeling artifacts and the need for live-cell imaging. Nat Methods. 2012. doi:10.1038/nmeth.1855
  7. Low LA, Mummery C, Berridge BR, Austin CP, Tagle DA. Organs-on-chips: into the next decade. Nat Rev Drug Discov. 2021. doi:10.1038/s41573-020-0079-3
  8. Bhatia SN, Ingber DE. Microfluidic organs-on-chips. Nat Biotechnol. 2014. doi:10.1038/nbt.2989
  9. Richter KN, Revelo NH, Seitz KJ, et al. Glyoxal as an alternative fixative to formaldehyde in immunostaining. EMBO J. 2018. doi:10.15252/embj.201695709

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