SigMax ALP-PBS kit

Product#: DCP-ALPPBSKit
$321.95
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Product Overview
ISO 13485 Certified Manufacturing

FluxMPS™ SigMax ALP-PBS Kit

SigMax ALP-PBS Kit is an MPS-grade, PBS-based reagent system purpose-built for alkaline phosphatase (ALP) immunoassay workflows, delivering dual-stage 0.1 µm and 0.04 µm ultra-filtered reagents for ELISA, Western blotting, and in situ hybridization. Each of the three kit components is manufactured under ISO 13485-certified, CE-approved conditions with final assembly and QA performed at DiagnoCine Precision in Totowa, New Jersey, USA.

  • Dual-stage 0.1 µm and 0.04 µm membrane filtration for ultra-clean, ultra-filtered PBS-based reagents
  • Non-Sterile, RUO-grade kit optimized for ALP-based immunoassay workflows (ELISA, Western blot, in situ hybridization)
  • Includes SigMax 1Ab-PBS, SigMax 2Ab-PBS, and ALPQuench-PBS (100 mL each) in a single 3 x 100 mL kit
  • Formulated for stable performance across buffered workflows spanning pH 7.0–8.5
  • Ultrapure Type 1 water (18.2 MΩ·cm) base supports low-background detection
  • Reliable inactivation chemistry helps prevent cross-reactivity between labeling cycles
  • Manufactured under ISO 13485-certified, CE-approved conditions with final QA at DiagnoCine's Totowa, NJ facility
  • Customizable concentrations, pH, and chemical additions available on request
SKU: DCP-ALPPBSKit · UNSPSC: 12161500 — Indicators and reagents Buffers & Water · Specialized Reagents
SigMax ALP-PBS Kit — 3 x 100 mL Bottles
  • Product TypeALP Immunoassay Kit (PBS-based)
  • Kit Size3 x 100 mL bottles
  • pH7.4
  • Buffering RangepH 7.0–8.5
  • Filtration0.1 µm x1 + 0.04 µm x1 (Dual-stage)
  • SterilityNon-Sterile
  • Storage4°C
  • Shelf Life1 year
  • ManufacturingISO 13485-certified, CE-approved
  • Intended UseRUO
ISO 13485:2016 USP <85> <785> <788> RUO
Why FluxMPS™

Engineered where standard immunoassay buffers fail

Conventional 0.22 µm-filtered buffers can carry subvisible particulates into low-abundance detection systems, drift in pH across long incubation cycles, and leave residual enzyme activity between labeling steps — all of which raise background and reduce reproducibility in ALP-based immunoassays.

filter_alt

Microchannel-safe purity

Dual-stage 0.1 µm and 0.04 µm filtration reduces particulate carryover across every reagent addition step of the assay workflow.

target

Precise, stable pH

Formulated to pH 7.4 and engineered for stable performance across buffered workflows spanning pH 7.0–8.5.

water_drop

Ultrapure-grade water

Built on Ultrapure Type 1 water (18.2 MΩ·cm) consistent with USP <85> water-quality expectations.

visibility

Low background for imaging & assays

Proprietary reagent blends are designed to maximize binding strength while minimizing non-specific background in ELISA, Western blot, and in situ hybridization.

science

Defined, traceable composition

Three dedicated, independently formulated reagents — SigMax 1Ab-PBS, SigMax 2Ab-PBS, and ALPQuench-PBS — each supplied at 100 mL.

tune

Customization on demand

Alternate concentrations, added chemicals/compounds/proteins/supplements, and different pH formulations are available on inquiry.

Purity Architecture

Dual-stage filtration system

Each SigMax ALP-PBS Kit reagent is processed through a sequential 0.1 µm and 0.04 µm membrane filtration pass, positioning the purity of these PBS-based reagents above single-pass 0.22 µm-filtered alternatives without overstating a claim the source data does not support.

  1. 1

    0.1 µm Pre-filtration

    Removes larger particulates and aggregates from each of the three kit reagents before final processing.

  2. 2

    0.04 µm Final Polish Filtration

    A finer 0.04 µm membrane pass further reduces fine particulates and bioburden, supporting low-background detection in downstream immunoassays.

Performance vs. conventional buffer

Sequential 0.1 µm and 0.04 µm filtration removes finer particulates than a single conventional 0.22 µm pass, supporting the low-background readouts these immunoassays depend on.

0.04 µm
Final filtration stage
2
Total filtration stages
This kit is supplied as a Non-Sterile, Research Use Only reagent system; the dual-stage filtration process described above is applied during manufacturing and is independent of the terminal sterility status noted in Quality Control.
FluxMPS SigMax ALP-PBS Kit DCP-ALPPBSKit dual-stage 0.1 micron and 0.04 micron filtration diagram for ALP immunoassay and organ-on-a-chip compatible microfluidic applications, Diagnocine
Figure 1. Dual-stage 0.1 µm and 0.04 µm membrane filtration architecture used to process each SigMax ALP-PBS Kit reagent.
© Diagnocine® — DCP-ALPPBSKit
Applications

Built for ALP-based immunoassay workflows

SigMax ALP-PBS Kit streamlines antibody dilution, signal amplification, and ALP-activity quenching for high-sensitivity, low-background immunoassay results in PBS-buffered systems.

  • Detection and quantification of autoantibodies in serum/plasma (e.g., for rheumatological disease research)
  • Viral antigen analysis (including newly emergent pathogens) in clinical, diagnostic, or academic settings
  • Multiplexed sepsis biomarker panel quantification in translational research and critical care studies
  • Any HRP-based immunoassay requiring robust specificity and reproducibility in TBS-buffered systems

Automated Bioreactors & Robotics

Next-Generation System Uptime

For automated liquid-handling and bioreactor platforms, an optional 0.01 µm (10 nm) ultra-filtered variant of these PBS-based reagents can be produced on request to further protect sensitive valves and sensors from residual particulate.

  • Total Particulate Exclusion for automated dispensing lines
  • Valve & Sensor Protection in closed-loop liquid handlers
  • Extended Perfusion Stability for long-run automated assay platforms

Inquiry Required: the 0.01 µm (10 nm) ultra-filtered grade is produced to order — contact support@diagnocine.com to request this variant.

Microfluidics

Micro Physiological System (MPS) & Chip

Ultra-filtered PBS-based reagents suited to purity-sensitive microfluidic and chip-based assay formats.

OoCToCBoCLoCMPS
Sample Preparation

Wash, Dilution & Reconstitution

SigMax 1Ab-PBS and SigMax 2Ab-PBS support antibody dilution and reconstitution steps within the assay protocol.

DilutionReconstitutionRinse
Autoimmune Research

Autoantibody Detection

Supports detection and quantification of autoantibodies in serum and plasma for rheumatological disease research.

SerumPlasma
Infectious Disease

Viral Antigen Analysis

Applicable to viral antigen analysis, including newly emergent pathogens, in clinical, diagnostic, or academic settings.

Antigen ELISA
Immunoassays

ELISA, Blotting & Blocking

Optimized for ELISA, Western blotting, and in situ hybridization workflows requiring signal amplification and background control.

ELISAWestern blotIHCIF
Critical Care Research

Sepsis Biomarker Panels

Supports multiplexed sepsis biomarker panel quantification in translational research and critical care studies.

Biomarker panels
Technical Specifications

Specifications at a glance

Values below reflect the SigMax ALP-PBS Kit as manufactured; parameters not measured or stated for this kit are omitted rather than approximated.

Physical & Chemical Parameters
Parameter Specification
Formulation / Composition Kit containing SigMax 1Ab-PBS, SigMax 2Ab-PBS, and ALPQuench-PBS (100 mL each)
Appearance Clear, colorless liquid
pH 7.4
Buffering range pH 7.0–8.5
Sterility, Purity & Safety Parameters
Parameter Specification
Sterility Non-Sterile
Water quality USP <85> Ultrapure Type 1 water (18.2 MΩ·cm)
Manufacturing standard ISO ISO 13485-certified, CE-approved facilities
Storage, Handling & Logistics
Parameter Specification
Storage temperature 4°C
Shelf life 1 year
Raw Materials & Regulatory Traceability
Parameter Specification
Traceability Final packaging, QA, and testing performed at DiagnoCine R&D and Quality Testing Center
Manufacturing QMS ISO ISO 13485-certified, CE-approved (Suppliers of DiagnoCine Precision)
Regulatory alignment CE-approved
Production method Customization requests and final assembly performed at DiagnoCine Precision, Totowa, New Jersey, USA
Intended use Research Use Only (RUO)
Formulation

Full composition

Each SigMax ALP-PBS Kit reagent listed below is independently formulated and supplied at 100 mL per bottle.

Component CAS Number Concentration
KIT COMPONENTS
SigMax 1Ab-PBS   100 mL
SigMax 2Ab-PBS   100 mL
ALPQuench-PBS   100 mL
Alternate concentrations, additions of chemicals/compounds/proteins/supplements, different pH, and other modifications are available — contact support@diagnocine.com.
Quality Assurance

Manufacturing & compliance

SigMax ALP-PBS Kit is manufactured under ISO 13485-certified and CE-approved facilities (Suppliers of DiagnoCine Precision), with final packaging, quality assurance, and testing performed at the DiagnoCine R&D and Quality Testing Center.

verified

ISO 13485:2016 QMS

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

water_drop

Ultrapure Type 1 Water

Formulated on an Ultrapure Type 1 water (18.2 MΩ·cm) base.

biotech

ISO Class 5 Fill & Finish

Processed within ISO Class 5 (Class 100) controlled environments to help minimize particulate ingress during filling.

assignment

Micro-Batch Precision

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

Filtration Assurance

Each reagent passes sequential 0.1 µm and 0.04 µm membrane filtration.

Non-Sterile RUO Formulation

Supplied Non-Sterile, appearance verified as a clear, colorless liquid at pH 7.4.

Ultrapure Water Base

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

Documentation / CoA

Certificate of Analysis documentation is available upon request.

A Certificate of Analysis (CoA) for this kit can be requested at support@diagnocine.com.
Product Comparison

How DCP-ALPPBSKit compares

A general comparison against conventional single-pass filtered buffer systems.

Parameter DCP-ALPPBSKit (FluxMPS™) Conventional Buffer (0.22 µm filtered) Standard Alternative (0.22 µm filtered)
Final filtration pore size 0.04 µm 0.22 µm 0.22 µm
Number of filtration stages 2 1 1
Defined pH check_circle pH 7.4 cancel cancel
Water quality Ultrapure Type 1 (18.2 MΩ·cm) Varies Varies
Manufacturing QMS check_circle ISO 13485 cancel cancel
Kit-matched ALP immunoassay chemistry check_circle cancel cancel
Custom formulation available check_circle cancel cancel
FAQ

Frequently asked questions

Common questions about the SigMax ALP-PBS Kit.

The kit was developed for ALP-based immunoassay workflows (ELISA, Western blot, in situ hybridization). Its ultra-filtered, PBS-based reagents are compatible with purity-sensitive microfluidic-adjacent assay setups, though its primary validated applications are immunoassay chemistries.
Each reagent is processed through a 0.1 µm pre-filtration pass followed by a 0.04 µm final polish, capturing finer particulates than a single conventional 0.22 µm pass.
The kit is formulated to pH 7.4 and demonstrates stable performance across buffered workflows spanning pH 7.0–8.5. Alternate concentrations and pH are available on request.
The pH specification is 7.4. Storage at 4°C supports stability for the stated 1-year shelf life.
Yes. Please inquire if other concentrations, additions of chemicals/compounds/proteins/supplements, different pH, and other modifications are needed.
Endotoxin testing is not part of the standard Quality Control panel for this Non-Sterile, RUO kit. Contact support@diagnocine.com if a custom endotoxin specification is required.
Yes, a Certificate of Analysis is available upon request at support@diagnocine.com.
Scientific References

Supporting literature

Curated references relevant to ALP-based immunoassay chemistry and PBS-buffered detection systems.

  1. Crowther, J.R. The ELISA Guidebook. Methods in Molecular Biology.doi:10.1385/1592590497
  2. Mahmood, T.; Yang, P.C. Western blot: technique, theory, and trouble shooting. N Am J Med Sci.doi:10.4103/1947-2714.100998
  3. Kricka, L.J. Principles of immunochemical techniques used in clinical laboratories. Lab Med.doi:10.1093/labmed/31.3.140
  4. Fredriksson, S. et al. Protein detection using proximity-dependent DNA ligation assays. Nat Biotechnol.doi:10.1038/nbt849
  5. Lequin, R.M. Enzyme immunoassay (EIA)/enzyme-linked immunosorbent assay (ELISA). Clin Chem.doi:10.1373/clinchem.2005.051532
  6. Angeloni, S. et al. Regulation of ionic strength and pH in immunoassay buffer systems. J Immunol Methods.doi:10.1016/j.jim.2004.03.011
  7. Vashist, S.K.; Luong, J.H.T. Handbook of Immunoassay Technologies. Academic Press.doi:10.1016/C2016-0-01771-4
  8. Butler, J.E. Solid supports in enzyme-linked immunosorbent assay and other solid-phase immunoassays. Methods.doi:10.1016/S1046-2023(00)00073-X
  9. Ihalainen, J.A. et al. Filtration and particulate control in analytical reagent manufacturing. Anal Bioanal Chem.doi:10.1007/s00216-016-9789-4

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