Bafilomycin A (10ug/mL)

Product#: DCP-BMA10UG
$233.79
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warning For Research Use Only (RUO). Not intended for clinical, diagnostic, or therapeutic use in humans.
Product Overview
ISO 13485 Certified Manufacturing

FluxMPS™ Bafilomycin A (10µg/mL)

Microfluidics Suitable, dual-stage ultra-filtered (0.1 µm ×1 + 0.04 µm ×1) DMSO stock solution of Bafilomycin A1, a potent and selective vacuolar H+-ATPase (V-ATPase) inhibitor. Supplied ready-to-use at 10 µg/mL for direct dilution into autophagy, lysosome, endosome, and membrane-trafficking assays, including microfluidic and organ-on-a-chip (OoC) culture systems.

  • Ready-to-use 10 µg/mL Bafilomycin A1 stock solution in DMSO for direct dilution into experimental systems
  • Potent, selective vacuolar H+-ATPase (V-ATPase) inhibitor that blocks proton translocation into acidic organelles
  • Widely used to distinguish increased autophagosome formation from impaired autophagic degradation in autophagy flux assays
  • Processed through Diagnocine's dual-stage filtration architecture (0.1 µm → 0.04 µm) for microchannel-safe purity
  • Confirmed free of DNase and RNase activity after 18-hour incubation testing with plasmid DNA and ribosomal RNA
  • Manufactured under an ISO 13485:2016 quality management system; final packaging and QC performed at Diagnocine, Totowa, NJ
  • Supplied as 10 mL (10 × 1 mL) single-use aliquots to minimize freeze-thaw cycles and preserve potency
  • Custom concentrations, chemical/compound/protein/supplement additions, and pH modifications available on request
SKU: DCP-BMA10UG Cell Biology Reagent · Autophagy / V-ATPase Inhibitor UNSPSC: 41116155 | Commodity: Molecular biology and cell culture growth media | (UNv260801)
Bafilomycin A (10µg/mL) — DMSO Solution
  • Active CompoundBafilomycin A1
  • Concentration10 µg/mL
  • SolventDMSO (Dimethyl sulfoxide)
  • AppearanceClear, colorless liquid
  • DNase ActivityNone detected
  • RNase ActivityNone detected
  • Filtration0.1 µm ×1 + 0.04 µm ×1 (Dual-stage)
  • Storage-80°C, in the dark
  • Shelf Life12 months from date of manufacture, unopened
  • Pack Size10 mL (10 × 1 mL)
ISO 13485:2016 DNase / RNase Tested RUO
Why FluxMPS™

Engineered where standard reagents fall short

Conventional 0.22 µm filtered research reagents can carry mycoplasma-scale particulates, subvisible aggregates, and inconsistent lot-to-lot purity — all of which can confound sensitive autophagy, lysosomal, and microfluidic assays. FluxMPS™ addresses these failure modes directly.

filter_alt

Microchannel-safe purity

Dual-stage 0.1 µm / 0.04 µm filtration removes particulates that can accumulate in narrow microfluidic channels and valves.

target

Precise mechanistic control

A single, well-characterized V-ATPase inhibitor delivered at a defined 10 µg/mL concentration for reproducible autophagy and lysosomal pH studies.

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Controlled solvent system

Formulated in DMSO for consistent solubility and accurate low-volume dosing across experimental replicates.

visibility

Low background for imaging

Supplied as a clear, colorless liquid to minimize interference with confocal and other optical readouts of lysosomal and autophagosome markers.

science

Confirmed nuclease-free

Each lot is tested for DNase and RNase activity to protect nucleic-acid-based assays run alongside treatment.

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Customization on demand

Alternate concentrations, additional chemicals, compounds, proteins, supplements, and pH adjustments available on request.

Purity Architecture

Dual-stage filtration system

Bafilomycin A (10µg/mL) is processed through Diagnocine's validated dual-stage filtration train, reaching a 0.04 µm final pore size. A dedicated 0.1 µm prefilter protects the 0.04 µm final filter, reducing particulate and mycoplasma-scale contamination risk ahead of final polish.

  1. 1

    0.1 µm Prefiltration

    Removes large particulates and aggregates from the DMSO solution, protecting the downstream 0.04 µm final filter.

  2. 2

    0.04 µm Final filtration — Polish

    Final polishing pass retaining sub-micron particulates and microaggregates that pass a conventional 0.22 µm filter.

Performance vs. conventional media

The dual-stage 0.1 µm / 0.04 µm train provides a finer, more consistent particulate cut-off than the single-stage 0.22 µm filtration typically used for standard research reagents.

0.04 µmFinal filtration cut-off
2Validated filtration passes
Sterility and mycoplasma risk are managed through this filtration process rather than asserted as a per-lot test result; the smallest known mycoplasma species measure approximately 0.2–0.3 µm, above the 0.1 µm pore rating of the prefiltration stage.
Grade: This product is Microfluidics Suitable, filtered to a 0.04 µm final cut-off. It is not an MPS Grade product — that designation is reserved for the 0.01 µm ultra nano-filtered line, which adds 0.02 µm and 0.01 µm stages after the 0.04 µm polish. For applications requiring the 0.01 µm cut-off, contact support@diagnocine.com.
Applications

Research applications

Bafilomycin A1 is a widely used pharmacological tool for probing autophagic flux, lysosomal acidification, and vesicular trafficking across a broad range of cell-based and microphysiological research systems.

Automated Bioreactors & Robotics

Next-Generation System Uptime

For automated dosing systems and long-duration perfusion bioreactors, Diagnocine also offers an optional 0.01 µm (10 nm) ultra nano-filtered MPS Grade variant of this reagent line, engineered to further reduce particulate load in automated fluid-handling systems.

  • Total Particulate Exclusion for long-duration automated dosing lines
  • Valve & Sensor Protection in closed-loop perfusion systems
  • Extended Perfusion Stability for multi-week automated culture protocols

Inquiry Required: The 0.01 µm MPS Grade variant is available by request; contact support@diagnocine.com for specifications and lead time.

Microfluidics

Micro Physiological System (MPS) & Chip

Direct dosing into closed microfluidic channels for autophagy and lysosomal pH studies.

OoCToCBoCLoCMPS
Cancer Biology

Autophagy in Tumor Cell Models

Used to dissect autophagy-dependent survival and drug-resistance mechanisms in tumor cell lines.

MCF-7MDA-MB-231HeLaA549
Stem Cell Biology

Autophagy in iPSC-Derived Models

Applied to study autophagic flux during differentiation and maturation of iPSC-derived lineages.

iPSC-NeuronsiPSC-CMiPSC-Hep
Vascular Biology

Endothelial Autophagy & Trafficking

Used to probe lysosomal and endosomal trafficking in vascular and primary cell models.

HUVECsHAECsPrimary hepatocytes
Metabolomics

Lysosomal Contribution to Metabolic Flux

Used alongside tracer-based methods to study how lysosomal inhibition alters cellular metabolism.

13C tracingNMR metabolomics
Live-Cell Imaging

LC3 Flux & Lysosomal pH Imaging

Widely used in confocal and biosensor-based imaging assays of autophagosome-lysosome fusion.

ConfocalBiosensorsTEER
Technical Specifications

Technical specifications

Physical, quality, storage, and regulatory parameters for Bafilomycin A (10µg/mL), DCP-BMA10UG.

Physical & Chemical Parameters
Parameter Specification
Formulation Bafilomycin A1 in DMSO
Concentration 10 µg/mL
Appearance Clear, colorless liquid
Solvent Dimethyl sulfoxide (DMSO)
Sterility, Purity & Safety Parameters
Parameter Specification
Sterility Filtered 0.1 µm membrane (single pass); designated Sterile per product documentation USP
Mycoplasma 0.1 µm mycoplasma-retentive prefiltration (not tested per lot); smallest known mycoplasma species measure 0.2–0.3 µm
DNase Activity None detected (18 hr incubation with plasmid DNA, room temperature)
RNase Activity None detected (18 hr incubation with ribosomal RNA, room temperature)
Storage, Handling & Logistics
Parameter Specification
Storage Temperature -80°C, in the dark
Shelf Life 12 months from date of manufacture, unopened
Pack Size 10 mL (10 × 1 mL)
Shipping Condition Contact for specification
Raw Materials & Regulatory Traceability
Parameter Specification
Manufacturing QMS ISO 13485-certified suppliers ISO; final packaging, QA, and testing at Diagnocine
UNSPSC 41116155 · Molecular biology and cell culture growth media (UNv260801)
Regulatory Alignment ISO 13485:2016
Production Method Custom assembly and QC at Diagnocine Precision, Totowa, New Jersey, USA
Intended Use For Research Use Only (RUO)
Formulation

Full composition

Bafilomycin A (10µg/mL) is a two-component formulation: the active pharmacological compound Bafilomycin A1 dissolved in a DMSO vehicle. Lot-release quality control attributes are listed in the third tab.

Component CAS Number Concentration
Bafilomycin A1 88899-55-2 10 µg/mL
Component CAS Number Concentration
Dimethyl sulfoxide (DMSO) 67-68-5 Vehicle, q.s. to volume
Attribute Method Result
Appearance Visual inspection Clear, colorless liquid
DNase activity Plasmid DNA incubation, 18 hr, room temperature None detected
RNase activity Ribosomal RNA incubation, 18 hr, room temperature None detected
Custom concentrations, formulation additions, and pH modifications are available on request — contact support@diagnocine.com.
Quality Assurance

Manufacturing & compliance

Bafilomycin A (10µg/mL) is produced under a controlled quality system with lot-level functional testing and final release performed at Diagnocine.

verified

ISO 13485 QMS

Manufactured under ISO 13485-certified suppliers of Diagnocine Precision.

filter_alt

Dual-stage filtration

Processed through a 0.1 µm prefilter and 0.04 µm final filter for microchannel-safe purity.

science

DNase / RNase Tested

Each lot is confirmed free of detectable DNase and RNase activity after 18-hour incubation testing.

location_on

Finished in Totowa, NJ

Final packaging, quality assurance, testing, and customization are completed at the Diagnocine R&D and Quality Testing Center, Totowa, New Jersey, USA.

Sterility

Filtered through a 0.1 µm membrane (single pass); designated Sterile per product documentation.

Functional Purity Testing

DNase and RNase activity testing performed on each lot using plasmid DNA and ribosomal RNA substrates.

Custom Formulation

Alternate concentrations, additional chemicals, compounds, proteins, supplements, and pH adjustments available on request.

Documentation

Certificate of Analysis available on request, including lot number and expiry.

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

How DCP-BMA10UG compares

A comparison of FluxMPS™ Bafilomycin A (10µg/mL) against representative classical cell-culture-grade reagent suppliers.

Parameter DCP-BMA10UG (FluxMPS™) Other Suppliers
Grade Microfluidics Suitable Varies by supplier; not typically specified
Filtration architecture Dual-stage: 0.1 µm ×1 + 0.04 µm ×1 Typically single-stage 0.22 µm filtration
Mycoplasma risk mitigation check_circle 0.1 µm mycoplasma-retentive prefiltration cancel Not typically stated at 0.22 µm
Endotoxin (release specification) FluxMPS™ — Not specified Corning classical liquid media — < 0.25 EU/mL
Sigma-Aldrich DMEM complete medium — ≤ 2 EU/mL
Gibco classical DMEM — Not specified (recorded per lot)
DNase / RNase testing check_circle Tested, none detected Varies by supplier
Manufacturing QMS ISO 13485:2016 Varies by supplier
Custom formulation check_circle Available on request Limited or not offered

Comparison figures from published supplier specifications, accessed 2026-09-02. Suppliers that publish no numeric endotoxin specification are shown as "Not specified".

FAQ

Frequently asked questions

Common questions about Bafilomycin A (10µg/mL), DCP-BMA10UG.

Yes. Bafilomycin A (10µg/mL) is compatible with microfluidic and organ-on-a-chip (OoC) culture systems for studying autophagy, lysosomal acidification, and vesicular trafficking. Its dual-stage filtered, ready-to-use DMSO format allows direct, low-volume dosing into closed-channel microfluidic devices.
This reagent is processed through a dedicated 0.1 µm prefilter followed by a 0.04 µm final filter, a finer cut-off than the 0.22 µm filtration commonly used for standard research reagents. The 0.1 µm stage is sized below the 0.2–0.3 µm diameter of the smallest known mycoplasma species, reducing particulate and mycoplasma-scale contamination risk ahead of the final polish.
Bafilomycin A1 has limited aqueous solubility, so it is supplied as a 10 µg/mL DMSO stock solution for accurate dosing and direct dilution into culture medium. Prepare working dilutions immediately before use and keep the final DMSO concentration in the culture system as low as practical for your assay, consistent with standard vehicle-control practice.
Bafilomycin A1 is used as an additive within your existing cell culture system and does not itself change the CO2 or temperature requirements of the base medium. Standard culture conditions for your cell model should be maintained; only the treatment concentration and exposure time need to be optimized for V-ATPase inhibition.
Yes. The DMSO stock is diluted directly into complete culture medium at the time of treatment. If additional serum, growth factors, or other protein-containing supplements are added to your medium separately, filter them through a 0.2 µm low-protein-binding PES or PVDF membrane rather than a smaller pore size, which can strip serum proteins and growth factors.
Store unopened vials at -80°C, in the dark. The 10 mL (10 × 1 mL) single-use aliquot format is designed to minimize freeze-thaw cycling; thaw only the aliquot needed for a given experiment and discard any unused, thawed material rather than refreezing.
Yes. A Certificate of Analysis is available on request and documents lot number, appearance, DNase and RNase activity results, filtration process, and expiry. Contact support@diagnocine.com to request the CoA for your lot.
Scientific References

Supporting literature

Key references on Bafilomycin A1 pharmacology, autophagy assays, and microfluidic/organ-on-a-chip research applications.

  1. Bowman EJ, Siebers A, Altendorf K. Bafilomycins: a class of inhibitors of membrane ATPases from microorganisms, animal cells, and plant cells. Proc Natl Acad Sci USA. 1988;85(21):7972-7976. doi:10.1073/pnas.85.21.7972
  2. Yoshimori T, Yamamoto A, Moriyama Y, Futai M, Tashiro Y. Bafilomycin A1, a specific inhibitor of vacuolar-type H(+)-ATPase, inhibits acidification and protein degradation in lysosomes of cultured cells. J Biol Chem. 1991;266(26):17707-17712. doi:10.1016/S0021-9258(19)47429-2
  3. Yamamoto A, Tagawa Y, Yoshimori T, Moriyama Y, Masaki R, Tashiro Y. Bafilomycin A1 prevents maturation of autophagic vacuoles by inhibiting fusion between autophagosomes and lysosomes in rat hepatoma cell line, H-4-II-E cells. Cell Struct Funct. 1998;23(1):33-42. doi:10.1247/csf.23.33
  4. Mauvezin C, Neufeld TP. Bafilomycin A1 disrupts autophagic flux by inhibiting both V-ATPase-dependent acidification and Ca-P60A/SERCA-dependent autophagosome-lysosome fusion. Autophagy. 2015;11(8):1437-1438. doi:10.1080/15548627.2015.1066957
  5. Klionsky DJ, et al. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition). Autophagy. 2021;17(1):1-382. doi:10.1080/15548627.2020.1797280
  6. Mizushima N, Yoshimori T, Levine B. Methods in mammalian autophagy research. Cell. 2010;140(3):313-326. doi:10.1016/j.cell.2010.01.028
  7. Huh D, Matthews BD, Mammoto A, Montoya-Zavala M, Hsin HY, Ingber DE. Reconstituting organ-level lung functions on a chip. Science. 2010;328(5986):1662-1668. doi:10.1126/science.1188302
  8. Huss M, Ingenhorst G, Konig S, et al. Concanamycin A, the specific inhibitor of V-ATPases, binds to the V(o) subunit c. J Biol Chem. 2002;277(43):40544-40548. doi:10.1074/jbc.M207345200
  9. Klionsky DJ, Elazar Z, Seglen PO, Rubinsztein DC. Does bafilomycin A1 block the fusion of autophagosomes with lysosomes? Autophagy. 2008;4(7):849-950. doi:10.4161/auto.6845

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