TBS with 5% Nonfat Soy Milk

Product#: DCP-DMB05
$27.50
DCP-DMB05
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ISO 13485 Certified Manufacturing

TBS with 5% Nonfat Soy Milk

A research-grade, Tris-buffered saline blocking and dilution buffer formulated with 5% nonfat soy milk for Western blotting and immunoassay workflows. Buffered at pH 7.4 with 20 mM Tris-Base and 150 mM Sodium Chloride. 0.1 µm filtration removes large particulates and aggregates, helping protect downstream applications.

  • 0.1 µm membrane filtration (single step)
  • Tris-buffered saline base: 20 mM Tris-Base, 150 mM Sodium Chloride, pH 7.4
  • 5% Nonfat Soy Milk blocking agent — casein-free, biotin-free, animal-protein-free
  • Prepared with Ultrapure Type 1 water (18.2 MΩ·cm)
  • DNase- and RNase-tested: none detected after 18 hr incubation at room temperature
  • Manufactured under ISO 13485-certified facilities
  • Customizable concentration, pH, and additive content available on request
SKU: DCP-DMB05 · 12161705 Basic Buffers Tris-based Buffers
TBS with 5% Nonfat Soy Milk — Western Blot Blocking Buffer
  • pH7.4
  • Tris-Base20 mM
  • Sodium Chloride150 mM
  • Nonfat Soy Milk5%
  • ProClin 300 (Preservative)0.05%
  • Filtration0.1 µm membrane filtration (single step)
  • AppearanceClear, Colorless Liquid
  • Storage4°C
  • Shelf Life1 year
  • SterilityNonsterile
ISO 13485:2016 USP <785> <788> RUO
Why This Blocking Buffer

Engineered where standard blocking buffers fall short

Conventional blocking buffers can carry residual particulates, batch-to-batch pH drift, and animal-derived proteins that interfere with sensitive detection chemistries. TBS with 5% Nonfat Soy Milk is designed to address each of these issues.

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0.1 µm filtered

0.1 µm filtration removes large particulates and aggregates, helping protect downstream applications.

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Precise, stable pH

Formulated at pH 7.4 with 20 mM Tris-Base and 150 mM Sodium Chloride to support optimal antibody-antigen interactions and reproducible blot-to-blot performance.

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Ultrapure-grade water

Prepared with Ultrapure Type 1 water (18.2 MΩ·cm) as the aqueous base for a low-background, reproducible buffer system.

visibility

Low-background blocking

Soymilk-based blocking has been reported to achieve a higher signal-to-noise ratio than nonfat dry milk, with effective blocking possible in as little as 10 seconds in some cases.[1]

science

Defined, traceable composition

Nonfat Soy Milk, ProClin 300, Tris-Base, and Sodium Chloride are each present at a controlled, stated concentration for consistent performance lot to lot.

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Customization on demand

Alternate concentrations, additional chemicals, compounds, proteins, supplements, different pH, or other modifications can be produced on request.

Purity Architecture

0.1 µm membrane filtration

DCP-DMB05 is filtered through a 0.1 µm membrane before final fill.

  1. 1

    0.1 µm Membrane Filtration

    Removes large particulates and aggregates, helping protect downstream applications.

Filtration

0.1 µm filtration removes large particulates and aggregates, helping protect downstream applications.

0.1 µm
Filtration membrane
1
Filtration step
DCP-DMB05 TBS with 5% Nonfat Soy Milk single-step 0.1 micron membrane filtration diagram, Diagnocine
Figure 1. DCP-DMB05, TBS with 5% Nonfat Soy Milk: 0.1 µm filtration removes large particulates and aggregates, helping protect downstream applications.
© Diagnocine® — DCP-DMB05
Applications

Where DCP-DMB05 is used

A Tris-buffered, soy-milk-based blocking and dilution buffer for Western blotting, immunoblotting, and related detection workflows.

Membrane Assays

Dot Blot & Protein Arrays

Blocks unoccupied binding sites on nitrocellulose or PVDF membranes before antibody probing in dot blot and protein array formats.

Dot blotSlot blotProtein arrays
Sample Preparation

Wash, Dilution & Reconstitution

Serves as a medium for diluting primary and secondary antibodies used in immunoblotting procedures.

DilutionReconstitutionRinse
Stem Cell Biology

iPSC-Derived Model Handling

Tris-buffered saline base compatible with wash and dilution steps used alongside iPSC-derived model workflows.

iPSC-NeuronsiPSC-CMiPSC-Hep
Vascular Biology

Endothelial & Primary Cell Models

Low-particulate buffer suitable for wash and dilution steps with primary and endothelial cell models.

HUVECsHAECsPrimary hepatocytes
Immunoassays

ELISA, Blotting & Blocking

Blocks non-specific binding sites on the membrane, reducing background noise and improving the signal-to-noise ratio in Western blots; TBS is recommended when using alkaline phosphatase (AP) conjugates since phosphate in PBS can interfere with AP activity.

ELISAWestern blotIHCIF
Live-Cell Imaging

Microscopy & Optical Sensing

Low-particulate, 0.1 µm-filtered formulation suited to imaging and optical sensing workflows.

ConfocalBiosensorsTEER
Technical Specifications

Product specifications

Measured and declared values for DCP-DMB05, as released by Diagnocine.

Physical & Chemical Parameters
Parameter Specification
Formulation Tris-Buffered Saline with 5% Nonfat Soy Milk
Appearance Clear, Colorless Liquid
pH USP <791> 7.4
Tris-Base 20 mM
Sodium Chloride 150 mM
Nonfat Soy Milk 5%
ProClin 300 0.05%
Sterility & Purity Parameters
Parameter Specification
Sterility / Filtration Nonsterile; 0.1 µm membrane filtration (single step)
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 ISO 13485-Certified Facility
Storage & Handling
Parameter Specification
Storage Temperature 4°C
Shelf Life 1 year
Raw Materials & Regulatory Traceability
Parameter Specification
Manufacturing QMS ISO 13485-Certified
Production Method 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 of DCP-DMB05 with its stated concentration, as released per lot.

Component CAS Number Concentration
Nonfat Soy Milk   5%
ProClin 300   0.05%
Tris-Base 77-86-1 20 mM
Sodium Chloride 7647-14-5 150 mM
Alternate concentrations, additions of chemicals, compounds, proteins, or supplements, different pH, and other modifications are available — please inquire at support@diagnocine.com.
Quality Assurance

Manufacturing & compliance

DCP-DMB05 is produced and released under a controlled quality system with defined testing at each stage.

verified

ISO 13485:2016 QMS

Manufactured under ISO 13485-certified supplier facilities.

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Ultrapure Type 1 Water

Prepared using Ultrapure Type 1 water (18.2 MΩ·cm) as the aqueous base.

biotech

Controlled Fill & Finish

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

assignment

Micro-Batch Precision

Customization requests and assembly are accomplished at Diagnocine Precision in Totowa, New Jersey, USA.

DNase Activity Testing

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

RNase Activity Testing

No RNase activity detected after incubation of ribosomal RNA with this product for 18 hr at room temperature.

Sterility & Filtration

Nonsterile; 0.1 µm membrane filtration (single step).

Documentation / CoA

A Certificate of Analysis is available on request for lot-specific release data.

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

How DCP-DMB05 compares

A side-by-side view of DCP-DMB05 against conventional dairy-milk-based TBS blockers and standard PBS-based blocking buffers.

Parameter DCP-DMB05 Conventional TBS + Dry Milk Blocker Standard PBS-Based Blocking Buffer
Animal-Protein-Free Blocking Agent check_circle cancel cancel
Casein-Free Formulation check_circle cancel cancel
Biotin-Free Formulation check_circle cancel cancel
Compatible with Alkaline Phosphatase (AP) Detection check_circle check_circle cancel
DNase / RNase Tested check_circle cancel cancel
ISO 13485-Certified Manufacturing check_circle cancel cancel
Custom Formulation Available check_circle cancel cancel
FAQ

Frequently asked questions

Common questions about DCP-DMB05, TBS with 5% Nonfat Soy Milk.

DCP-DMB05 undergoes a single 0.1 µm membrane filtration step, which removes large particulates and aggregates, helping protect downstream applications.
DCP-DMB05 is formulated at pH 7.4 with 20 mM Tris-Base and 150 mM Sodium Chloride. Other concentrations, pH values, or additional chemicals, compounds, proteins, or supplements can be produced on request — contact support@diagnocine.com.
The release specification for this lot is pH 7.4; a separate measurement temperature is not designated in the product documentation. The buffer is stored at 4°C with a shelf life of 1 year to help maintain formulation integrity.
Yes. Additions of chemicals, compounds, proteins, or supplements, along with different pH or concentrations, can be accommodated — please inquire at support@diagnocine.com.
See the lot Certificate of Analysis (CoA); contact support@diagnocine.com.
Yes, a lot-specific Certificate of Analysis is available on request from support@diagnocine.com, covering appearance, pH, filtration process, and DNase/RNase test results.
Scientific References

Supporting literature

Citations and curated literature relevant to soymilk-based blocking and Tris-buffered saline chemistry.

Citations

  1. Galva, C., Gatto, C., & Milanick, M. (2012). Soymilk: an effective and inexpensive blocking agent for immunoblotting. Analytical Biochemistry, 426(1), 22-23. doi:10.1016/j.ab.2012.03.028

Supporting Literature

  1. Towbin, H., Staehelin, T., & Gordon, J. (1979). Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proceedings of the National Academy of Sciences, 76(9), 4350-4354. doi:10.1073/pnas.76.9.4350
  2. Mahmood, T., & Yang, P. C. (2012). Western blot: technique, theory, and trouble shooting. North American Journal of Medical Sciences, 4(9), 429-434. doi:10.4103/1947-2714.100998
  3. Good, N. E., Winget, G. D., Winter, W., Connolly, T. N., Izawa, S., & Singh, R. M. (1966). Hydrogen ion buffers for biological research. Biochemistry, 5(2), 467-477. doi:10.1021/bi00866a011

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