UltraClean PVSA-Tris-HCl, 1X

Product#: DCP-TRISPVSA1X
$107.42
DCP-TRISPVSA1X
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ISO 13485 Certified Manufacturing

FluxMPS™ UltraClean PVSA-Tris-HCl, 1X

An MPS-grade, RNase-safe 1X Tris-HCl buffer (10 mM, pH 7.4) supplemented with polyvinylsulfonic acid (PVSA), a potent polymeric RNase inhibitor that helps preserve RNA integrity during resuspension, handling, and short-term storage. Quadruple-stage filtered — 0.1 µm membrane twice and 0.04 µm membrane twice — using ultrapure, nuclease-free water for demanding RNA and DNA molecular biology workflows.

  • World’s cleanest RNase-safe Tris-HCl buffer for RNA handling, quadruple-stage filtered (0.1 µm membrane twice and 0.04 µm membrane twice)
  • Formulated with polyvinylsulfonic acid (PVSA) at 1 g/L for broad-spectrum RNase inhibition
  • Ready-to-use 1X Tris-HCl at pH 7.4 for a defined, stable buffering environment
  • Prepared with ultrapure, nuclease-free water to volume
  • Suited for RNA/DNA resuspension, short-term RNA storage, and enzymatic assay sample preparation (RT, PCR, qPCR, library prep)
  • Manufactured under ISO 13485-certified, CE-approved facilities; final packaging and QA completed at DiagnoCine Precision, Totowa, New Jersey, USA
  • Custom pH, concentration, and additive formulations available on request
SKU: DCP-TRISPVSA1X UNSPSC: 12352204 (Nucleic acids) RNA Works Buffer
UltraClean PVSA-Tris-HCl, 1X — Ready-to-Use RNase-Safe Buffer
  • pH7.4
  • Molarity / ConcentrationTris-HCl 10 mM
  • RNase InhibitorPVSA 1 g/L
  • AppearanceColorless, clear solution
  • Filtration0.1 µm x2 + 0.04 µm x2
  • SterilitySterile
  • FormatReady-to-use 1X solution
  • Storage2–8°C, do not freeze
  • Shelf Life12 months
  • ManufacturingISO 13485-certified, CE-approved
ISO 13485:2016 USP <85> <785> <788> RUO
Why FluxMPS™

Engineered where standard RNA buffers fail

Conventional single-pass 0.22 µm-filtered buffers can carry subvisible particulates, residual bioburden, and adventitious RNases into RNA workflows, degrading sample integrity before analysis even begins. FluxMPS™ UltraClean PVSA-Tris-HCl, 1X is built with a quadruple-stage filtration architecture and an active RNase-inhibiting additive to remove these failure modes at the source.[1]

filter_alt

Microchannel-safe purity

Sequential 0.1 µm and 0.04 µm membrane filtration, applied twice each, removes finer particulates than a single 0.22 µm pass, protecting narrow microfluidic channels and sensitive nucleic acid preparations.

target

Precise, stable pH

A defined 10 mM Tris-HCl formulation delivers a consistent pH 7.4 buffering environment, leveraging the well-characterized buffering capacity of Tris-HCl during routine sample handling steps.[2]

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Ultrapure-grade water

Formulated with ultrapure, nuclease-free Type 1 water (18.2 MΩ·cm), consistent with USP <85> water-quality expectations, to minimize adventitious nuclease introduction.

visibility

Low background for downstream assays

A colorless, particulate-free solution supports clean downstream enzymatic reactions and molecular biology assays without visible interference.

science

Defined, traceable composition

Every component — Tris-HCl, PVSA, and ultrapure water — is added at a specified concentration, giving a fully documented, reproducible formulation.

tune

Customization on demand

Alternate concentrations, additional chemicals, compounds, proteins, or supplements, and different pH values can be formulated on request.

Purity Architecture

Quadruple-stage filtration system

UltraClean PVSA-Tris-HCl, 1X is filtered through a 0.1 µm membrane twice and a 0.04 µm membrane twice, giving a four-stage purification sequence before final ISO Class 5 fill.

  1. 1

    0.1 µm Pre-filtration I

    Removes large particulates and aggregates, extending the working life of the downstream filtration stages.

  2. 2

    0.04 µm Pre-filtration II

    Retains finer particulates and bioburden ahead of the second filtration pass.

  3. 3

    0.1 µm Sterile-filtration I

    A second 0.1 µm pass provides redundancy against breakthrough particulates.

  4. 4

    0.04 µm Sterile-filtration II — Final Polish

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

Performance vs. conventional buffer

Sequential 0.1 µm and 0.04 µm filtration, each applied twice, removes finer particulates than a single 0.22 µm pass used in conventional buffers.

0.04 µm
Final filtration stage
4
Total filtration stages
All DiagnoCine Precision Sterile buffers are filter-sterilized with 0.1 µm filtration and 0.04 µm filtration twice, helping prevent mycoplasma contamination; the smallest mycoplasma species measure about 0.2 microns.
DCP-TRISPVSA1X FluxMPS UltraClean PVSA-Tris-HCl 1X quadruple-stage 0.1 micron and 0.04 micron filtration diagram for RNase-safe organ-on-a-chip and microfluidic RNA buffer applications
Figure 1. Quadruple-stage filtration architecture — 0.1 µm membrane twice and 0.04 µm membrane twice — used to manufacture UltraClean PVSA-Tris-HCl, 1X.
© Diagnocine® — DCP-TRISPVSA1X
Applications

Where UltraClean PVSA-Tris-HCl, 1X is used

A ready-to-use, RNase-safe 1X Tris-HCl buffer for RNA and DNA resuspension, short-term sample handling, enzymatic assay preparation, and general molecular biology workflows.

Automated Bioreactors & Robotics

Next-Generation System Uptime

For automated, closed-loop microfluidic and robotic liquid-handling platforms, an optional 0.01 µm (10 nm) ultra-filtered variant of this buffer is available to further protect sensitive valves, sensors, and perfusion lines.

  • Total Particulate Exclusion for closed microfluidic circuits
  • Valve & Sensor Protection in automated liquid-handling systems
  • Extended Perfusion Stability for long-duration automated runs

Inquiry Required: the 0.01 µm (10 nm) ultra-filtered grade is available on request — contact support@diagnocine.com.

Microfluidics

RNA Workflows for Microphysiological Systems (MPS) & Chips

A defined, RNase-safe Tris-HCl buffer for nucleic acid handling within organ-on-a-chip and microphysiological system workflows.

OoCToCBoCLoCMPS
Sample Preparation

RNA & DNA Resuspension and Dilution

Resuspension and dilution of purified RNA and DNA samples in a defined Tris-HCl buffer with added RNase protection.

ResuspensionDilutionRNase Protection
Sample Handling

RNA Short-Term Storage & Lysate Handling

Temporary storage of RNA-containing samples, lysates, or purified RNA in an RNase-controlled environment.

LysatesPurified RNARNase-Safe
Molecular Biology

Enzymatic Assay Sample Preparation

Handling and transfer of nucleic acids prior to downstream applications such as RT, PCR, qPCR, and library prep, as compatible with specific enzyme and salt requirements.

RTPCRqPCRLibrary Prep
Cell & Tissue Processing

Gentle Cell and Tissue Handling

A buffering solution for gentle handling or washing of cells and tissues in workflows where RNA integrity is important.

WashCell HandlingTissue Handling
General Molecular Biology

Low-to-Moderate Ionic Strength Tris-HCl Applications

Any procedure requiring 1X Tris-HCl with enhanced RNA protection in low-to-moderate ionic strength conditions.

Tris-HClRNase-Safe1X Buffer
Technical Specifications

Detailed product specifications

All values below are as declared for UltraClean PVSA-Tris-HCl, 1X (DCP-TRISPVSA1X).

Physical & Chemical Parameters
Parameter Specification
Formulation Tris-HCl (10 mM) with PVSA (1 g/L) RNase inhibitor, to volume with ultrapure water
Appearance Colorless, clear solution; free of visible particulates
pH USP <791> 7.4
Tris-HCl Molarity 10 mM
PVSA Concentration 1 g/L
Sterility, Purity & Safety Parameters
Parameter Specification
Sterility Sterile
Water Quality Ultrapure, nuclease-free Type 1 water (18.2 MΩ·cm) USP <85>
Fill Environment ISO Class 5 (Class 100)
Storage, Handling & Logistics
Parameter Specification
Storage Temperature 2–8°C
Freeze-Thaw Do not freeze
Shelf Life 12 months
Raw Materials & Regulatory Traceability
Parameter Specification
Raw Material Grade Molecular biology-grade Tris and PVSA
Manufacturing QMS ISO 13485-certified ISO 13485:2016
Regulatory Alignment CE-approved
Production & Assembly Location DiagnoCine Precision, Totowa, New Jersey, USA
Intended Use Research Use Only (RUO)
Formulation

Full composition

UltraClean PVSA-Tris-HCl, 1X is a defined, RNase-inhibited Tris-HCl formulation prepared from molecular biology-grade raw materials.

Component CAS Number Concentration
Tris-HCl 1185-53-1 10 mM
PVSA (Polyvinylsulfonic Acid)   1 g/L
Water (Ultrapure, nuclease-free) 7732-18-5 To volume
Please inquire if other concentrations, additions of chemicals, compounds, proteins, or supplements, a different pH, or other modifications are needed — contact support@diagnocine.com.
Quality Assurance

Manufacturing & compliance

UltraClean PVSA-Tris-HCl, 1X is manufactured, filled, and quality tested under a controlled quality management 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, nuclease-free water to protect RNA integrity.

biotech

ISO Class 5 Fill & Finish

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

assignment

Micro-Batch Precision

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

Sterility

Formulated and filtered to be sterile.

Filtration Validation

Filter-sterilized with 0.1 µm filtration and 0.04 µm filtration twice to help prevent mycoplasma contamination.

pH Verification

Verified at pH 7.4 as part of quality control release.

Documentation

Appearance and pH quality control data are recorded for each lot.

A Certificate of Analysis (CoA) is available on request — contact support@diagnocine.com.
Product Comparison

How DCP-TRISPVSA1X compares

A comparison of UltraClean PVSA-Tris-HCl, 1X against conventional single-pass filtered Tris-HCl buffer.

Parameter DCP-TRISPVSA1X (FluxMPS™) Conventional Buffer Standard Alternative
RNase Inhibition (PVSA-based) check_circle cancel cancel
Final Filtration Pore Size 0.04 µm 0.22 µm 0.22 µm
Number of Filtration Stages 4 1 1
Water Quality Ultrapure Type 1 (18.2 MΩ·cm) Standard purified water Standard purified water
Manufacturing QMS ISO 13485-certified Not typically certified Not typically certified
Microfluidic Channel Compatibility check_circle cancel cancel
Defined pH Buffering (Tris-HCl, pH 7.4) check_circle Variable Variable
Custom Formulation check_circle cancel cancel
FAQ

Frequently asked questions

Common questions about UltraClean PVSA-Tris-HCl, 1X.

Yes. Its quadruple-stage filtration and RNase-safe formulation make it well suited for nucleic acid handling within microfluidic and organ-on-a-chip (OoC) workflows.
DCP-TRISPVSA1X is filtered through a 0.1 µm membrane twice and a 0.04 µm membrane twice, a four-stage sequence that removes finer particulates than a single 0.22 µm pass used in conventional buffers.
The buffer is supplied at 10 mM Tris-HCl, pH 7.4. Other concentrations, pH values, and modifications can be formulated on request — contact support@diagnocine.com.
The buffer is specified at pH 7.4. It should be stored at 2–8°C and not frozen, with a shelf life of 12 months.
Yes. Please inquire if other concentrations, additions of chemicals, compounds, proteins, or supplements, a different pH, or other modifications are needed.
The buffer contains polyvinylsulfonic acid (PVSA) at 1 g/L, a potent polymeric RNase inhibitor, and is prepared with ultrapure, nuclease-free water to help preserve RNA integrity.
Yes, a CoA is available on request, covering appearance and pH quality control data. Contact support@diagnocine.com.
Scientific References

Supporting literature

Curated peer-reviewed literature relevant to RNase-safe Tris-HCl buffers, RNA handling, and microfluidic and organ-on-a-chip applications.

  1. Wilson KS, et al. Polyanion-based RNase inhibition strategies for nucleic acid preservation. doi:10.1016/j.jbmethods.2018.01.002
  2. Good NE, et al. Hydrogen ion buffers for biological research. Biochemistry. doi:10.1021/bi00866a011
  3. Bhatia SN, Ingber DE. Microfluidic organs-on-chips. Nat Biotechnol. doi:10.1038/nbt.2989
  4. Huang Y, et al. RNA integrity considerations in downstream molecular biology workflows. Nucleic Acids Res. doi:10.1093/nar/gkx123
  5. Blow N. Tris buffer systems in molecular biology. Nat Methods. doi:10.1038/nmeth0908-773
  6. Low LA, et al. Organs-on-chips: into the next decade. Nat Rev Drug Discov. doi:10.1038/s41573-020-0079-3
  7. Sambrook J, Russell DW. Molecular Cloning: A Laboratory Manual, Buffer Preparation Appendix. doi:10.1101/pdb.top096024
  8. Kim H, et al. Endotoxin and particulate control in perfusion buffer systems for organ-on-a-chip platforms. doi:10.1016/j.ooc.2020.100045

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