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Conductive Pipette Tips Compatible with Bio-Rad EVOLIS, 300 µL & 1100 µL

Conductive Pipette Tips Compatible with Bio-Rad EVOLIS in 300 µL and 1100 µL system-designated formats.

  • Black conductive polypropylene for capacitive liquid-level detection
  • 96 tips per automation rack
  • 300 µL and 1100 µL variants on one clearly structured product page
  • Samples, technical documents and international supply support

Request a compatibility sample or quotation

PRODUCT DETAILS

Conductive Pipette Tips Compatible with Bio-Rad EVOLIS

Puretest EVOLIS-compatible conductive pipette tips are designed for automated sample and reagent transfers on Bio-Rad EVOLIS microplate immunoassay systems. The family includes 300 µL and 1100 µL system-designated formats in 96-position automation racks, allowing laboratories, distributors and service providers to qualify one dependable second-source family for routine EVOLIS workflows.

Black conductive polypropylene supports the capacitive liquid-level and clot-detection functions used by the EVOLIS pipetting system. Consistent tip-cone geometry, rack registration and molded orifice quality are essential to dependable pickup, sealing, aspiration, dispense and ejection across the full 96-position rack.

Compatibility must be confirmed with the exact EVOLIS model, installed pipetting configuration, software method, rack carrier and liquid-handling protocol. Puretest recommends evaluation samples and method-specific qualification before routine, regulated or validated use.

Product Highlights

  • Two-volume family: 300 µL and 1100 µL system-designated conductive tips for low-to-large-volume EVOLIS transfers.
  • EVOLIS-compatible interface: engineered for compatible Bio-Rad EVOLIS and EVOLIS Twin Plus automation contexts, subject to exact-system qualification.
  • Conductive polypropylene: black conductive material supports capacitive liquid-level and clot-detection workflows.
  • 96-position automation rack: consistent rack registration for automated pickup and walkaway processing.
  • Low-retention fluid path: smooth internal surfaces and controlled orifice geometry help reduce residual liquid and transfer variability.
  • Qualification support: samples, drawings, material declarations and current quality documents can be supplied for confirmed configurations.
  • International supply: support for laboratories, diagnostic distributors, OEM/private-label projects and recurring bulk procurement.

Tip Structure and Functional Design

An EVOLIS-compatible tip is part of a complete mechanical and sensing system. The upper cone must create a repeatable seal on the pipetting adapter; the conductive polymer must provide stable capacitive response; the shaft must maintain sufficient rigidity and labware clearance; and the distal orifice must support predictable aspiration and dispense behavior. The rack must also locate all 96 tips consistently so pickup force and tip height remain uniform across the instrument deck.

The 300 µL and 1100 µL variants use different shaft lengths and working-volume envelopes. They must not be interchanged only because both tips appear similar in a rack. Select the variant required by the EVOLIS method and confirm liquid class, immersion depth, transfer volume and destination-labware clearance during qualification.

Technical Specifications

Specification 300 µL Variant 1100 µL Variant
System designation 300 µL conductive tip 1100 µL conductive tip; some compatible-tip catalogs describe this family as 1000 µL nominal
Primary use Sample, predilution and reagent transfers within the validated method range Large-volume transfers; EVOLIS literature describes usable system transfers up to 1000 µL
Material Black conductive polypropylene Black conductive polypropylene
Detection support Capacitive liquid-level and clot-detection workflows Capacitive liquid-level and clot-detection workflows
Rack format 96 tips per automation rack 96 tips per automation rack
Filter / sterility Confirmed by exact quoted SKU Confirmed by exact quoted SKU
Case quantity Confirmed in quotation according to rack and packaging configuration Confirmed in quotation according to rack and packaging configuration

The values above describe the compatible product family and system context. Exact performance, purity, sterility, filter construction, case quantity and documents are controlled by the quoted Puretest SKU and should be confirmed before purchase.

Platform and Method Compatibility

Bio-Rad literature describes the EVOLIS platform as an automated pipettor, incubator, washer, reader and data-management system for EIA microplate assays. Its pipette-tip station accommodates five racks of 96 disposable tips and uses 300 µL or 1100 µL tip formats. Conductive tips support capacitive liquid-level and clot detection during automated sample and reagent processing.

Qualification Item Why It Matters Recommended Check
Analyzer and configuration EVOLIS family configurations and local methods may differ Provide the exact analyzer model, serial/configuration and current tip reference
Tip volume 300 µL and 1100 µL variants serve different transfer ranges Match the method-defined tip family; do not substitute only by appearance
Rack seating and pickup Registration and pickup force influence tip retention and walkaway reliability Test every deck position and representative rows/columns
Conductive response Capacitive sensing depends on material consistency and instrument settings Verify liquid-level and clot-detection behavior with routine tubes and reagents
Liquid class Viscosity, surface tension, foam and volatility affect transfer performance Evaluate aspiration/dispense speed, depth, delay, air gap and residual volume
Ejection and waste path Incomplete ejection can interrupt automated processing Confirm clean release across a full rack and representative run

Quality, Purity and Configuration Control

For diagnostic and high-throughput work, order the exact configuration required by the laboratory quality system. Conductive material, filter design, sterility status and packaging method can change pickup behavior, usable capacity and contamination-control performance. Puretest therefore identifies each sellable configuration by SKU and supplies the documents applicable to that configuration.

  • Medical- or laboratory-grade conductive polypropylene configuration as quoted
  • Controlled molding for tip-cone, shaft and orifice consistency
  • 96-position rack inspection for registration and automated pickup
  • Lot identification and traceability options
  • Sterility, nuclease, pyrogen/endotoxin and material documents available only where specified for the selected SKU
  • Evaluation samples for mechanical, sensing and liquid-handling qualification

Typical Applications

  • Automated EIA and ELISA microplate processing
  • Primary-sample handling and predilution
  • Reagent transfer and assay setup
  • Infectious-disease and autoimmune serology workflows
  • High-throughput diagnostic laboratories
  • Routine replacement and second-source consumable qualification

Recommended Evaluation Workflow

  1. Identify the installed system: provide the exact EVOLIS model, current tip reference, method volumes and rack format.
  2. Select the correct variant: choose 300 µL or 1100 µL according to the method and transfer range.
  3. Check mechanical fit: verify rack seating, pickup, tip retention, clearance and ejection across representative positions.
  4. Check sensing: confirm liquid-level and clot-detection behavior with the actual sample tubes and reagents.
  5. Check liquid handling: evaluate minimum, routine and maximum critical transfers using the intended liquid classes.
  6. Document approval: retain the approved SKU, lot documents, instrument configuration and method settings before routine use.

Ordering Information

Information to Provide Example / Purpose
Required volume 300 µL or 1100 µL system-designated format
Analyzer information EVOLIS model/configuration and current consumable reference
Filter and sterility State whether filtered, sterile or specific purity documents are required
Method information Critical volumes, sample/reagent type and detection requirements
Commercial requirement Sample quantity, annual demand, destination, private label or distributor program

Frequently Asked Questions

Are these Eppendorf epMotion tips?

No. This page covers conductive robotic tips intended for compatible Bio-Rad EVOLIS system contexts. Eppendorf epT.I.P.S. Motion products may use similar capacity labels, but platform compatibility must not be inferred from capacity or appearance.

Is the large-volume tip 1000 µL or 1100 µL?

Bio-Rad EVOLIS system literature uses the 1100 µL tip designation, while some compatible-tip suppliers describe the same large-volume family as 1000 µL nominal. Puretest uses 1100 µL system designation on this page and confirms the exact quoted SKU before order.

Do the tips support liquid-level detection?

The black conductive polypropylene configuration is intended to support capacitive liquid-level and clot-detection workflows. Final performance must be verified on the customer’s exact analyzer and method.

Are filtered and sterile versions available?

Filter, sterility and purity requirements must be specified at quotation. Only the properties stated for the exact quoted SKU and its current documents should be used for validation or regulatory records.

Can I request samples before a bulk order?

Yes. Sample qualification is strongly recommended. Send the analyzer model, current tip reference, required volume, filter/sterility needs and target application so Puretest can prepare the correct sample plan.

Request Samples, Technical Documents or a Quotation

For a fast compatibility review, include your EVOLIS model, current consumable reference or photographs, required 300 µL/1100 µL format, filter and sterility requirements, annual consumption and destination country.

Contact Puretest to request EVOLIS-compatible tip samples or a quotation.

Bio-Rad and EVOLIS are trademarks of their respective owner. Puretest is an independent compatible-consumables supplier and is not affiliated with or endorsed by Bio-Rad Laboratories. Compatibility statements are application-specific and require customer qualification.

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