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10 µL Robotic Pipette Tips Compatible with Agilent Bravo, 384-Format

10 µL Robotic Pipette Tips Compatible with Agilent Bravo, 384-Format for compatible automated liquid-handling workflows.

  • Platform, head and rack selection guidance
  • Technical specification and configuration tables
  • Full-head qualification workflow
  • Samples, technical documents and international supply support

Request a compatibility sample or quotation

PRODUCT DETAILS

10 µL Robotic Pipette Tips Compatible with Agilent Bravo, 384-Format

Puretest 10 µL robotic pipette tips are intended for assay miniaturization, low-volume reagent dispensing and high-density 384-well plate preparation. This page is structured for automation engineers, laboratory managers, procurement teams, distributors and OEM buyers who need an auditable selection process rather than a generic statement that a tip “fits.”

Agilent platform literature associates the 10 µL tip family with an approximate 0.3–10 µL transfer range and 96ST or 384ST pipetting-head workflows. This is a platform reference, not a blanket performance claim for every Puretest configuration. The installed head, rack carrier, liquid class and sellable Puretest SKU must be confirmed together.

Reliable automated pipetting depends on the complete system: instrument, installed head or channel, tip-cone interface, rack, carrier, software tip definition, liquid class, source and destination labware and liquid properties. Puretest recommends sample qualification with the intended method before routine or validated use.

Product Highlights

  • Application-focused family: 10 µL selection for assay miniaturization, low-volume reagent dispensing and high-density 384-well plate preparation.
  • Automation format: 384-format rack for compatible Agilent Bravo workflows.
  • Transparent option control: filter, sterility, conductivity, special geometry and packaging are confirmed by exact SKU.
  • Full-head qualification: structured checks for rack seating, pickup, seal, liquid class, channel consistency and ejection.
  • Document support: current material, cleanliness, sterility and lot records can be requested for qualified configurations.
  • Commercial support: evaluation samples, international supply, distributor and OEM/private-label programs are available.

Tip Structure and Functional Design

A robotic pipette tip functions as part of a mechanical and fluidic system. Cone-interface consistency influences sealing and pressure behavior; shaft geometry affects labware access; the distal section influences residual liquid and dispense behavior; and rack registration determines multi-channel pickup reliability. Filter placement, orifice geometry and material can each change usable volume or liquid-class performance.

Qualification must therefore use the exact sellable configuration. A change from non-filtered to filtered, standard to extended or wide-bore, clear to conductive, or non-sterile to sterile supply should be documented and the relevant mechanical and liquid-handling checks repeated.

Technical Specifications and Selection Notes

Specification Family / Platform Context Qualification or Ordering Note
Nominal family 10 µL Select for low-volume methods; verify the lowest critical transfer
Platform literature range Approximately 0.3–10 µL Reference context only; customer qualification is required
Rack density 384-format Confirm carrier, pickup coordinates, rack height and lid clearance
Head context Compatible Bravo 96ST / 384ST workflows Provide the exact installed head and method
Material / sensing Clear or conductive configuration by SKU Confirm whether conductive liquid-level detection is required
Filter / sterile / nested Configuration-dependent Confirm each option and current documentation in the RFQ
Tip geometry Standard low-volume geometry; special variants by SKU Do not substitute a visually similar tip without qualification

Platform-literature values describe the compatible automation context; they do not create a universal Puretest performance guarantee. Puretest will confirm the actual quoted configuration, available documents and sample plan.

Platform, Head and Rack Compatibility

Agilent platform literature associates the 10 µL tip family with an approximate 0.3–10 µL transfer range and 96ST or 384ST pipetting-head workflows. This is a platform reference, not a blanket performance claim for every Puretest configuration. The installed head, rack carrier, liquid class and sellable Puretest SKU must be confirmed together.

Qualification Item Why It Matters Recommended Check
Instrument and head One platform family may support multiple heads and tip definitions Provide the exact platform, installed head/pod and software method
Rack and carrier Footprint, height and registration determine reliable pickup Confirm carrier, deck coordinates, lid clearance and rack seating
Pickup, seal and ejection Mechanical consistency affects pressure, retention and error rate Inspect every active channel across representative deck positions
Liquid class Viscosity, volatility, surface tension and foaming change transfer behavior Tune speeds, delays, immersion depth, pre-wetting, air gaps and tip touch
Critical transfer points A nominal family does not guarantee every method volume Test minimum, routine and maximum critical volumes with real liquids
Variant changes Filters, material, geometry and sterility can alter behavior Requalify each materially different sellable configuration

For second-source qualification, send the exact platform, installed head or pod, current tip reference or drawing when available, rack carrier, target volumes, liquids, filter and sterility needs and annual consumption.

Available Material, Filter and Packaging Configurations

Configuration Typical Reason to Select What to Confirm
Clear / non-conductive Visual setup and methods without conductive sensing Material, sterility and filter state
Conductive Compatible liquid-level-detection strategies Instrument hardware, head and method support
Filtered Aerosol-barrier or contamination-sensitive work Filter material and usable volume
Nested / stackable Longer unattended runs and reduced deck interventions Nest count, deck height and gripper access

Not every option is necessarily available in every volume and rack combination. The final quotation should identify material, conductivity, filter state, sterility, rack format, wrapping, case quantity and required technical documents.

Typical Applications

  • PCR and qPCR setup
  • assay miniaturization
  • low-volume normalization
  • compound transfer
  • 384-well reagent dispensing

At sub-10 µL volumes, evaporation, pre-wetting, aspiration depth, liquid surface behavior and dispense position can dominate performance. Qualification should include the lowest critical transfer rather than testing only a convenient midpoint.

Method Development and Qualification Workflow

  1. Verify mechanical fit: inspect rack seating, pickup, vertical alignment, seal, retention and ejection across all active channels.
  2. Verify deck integration: confirm carrier, rack height, lid clearance, pickup coordinates and access from required positions.
  3. Configure sensing: confirm whether conductive liquid-level detection or another detection strategy is required.
  4. Optimize the liquid class: evaluate aspiration and dispense speeds, delays, immersion depth, pre-wetting, air gaps, mixing and tip touch.
  5. Challenge real liquids: include aqueous, viscous, volatile, foaming, particulate or low-surface-tension liquids used by the process.
  6. Measure performance: verify accuracy, precision, residual volume, channel consistency, carryover risk and error recovery.
  7. Record the approved setup: document tip SKU, lot, rack, instrument/head and liquid-class version for change control.

Quality, Sterility and Technical Documentation

Automation consumables may require material information, product specifications, irradiation or sterility records, lot traceability, certificate of analysis and RNase/DNase or pyrogen/endotoxin declarations. Availability and limits depend on the exact SKU and current production configuration.

Do not transfer a claim from another capacity, material or package format. State required documents in the RFQ so Puretest can confirm what applies before order placement. Customers remain responsible for final qualification in regulated or validated workflows.

Packaging, Logistics and Supply Continuity

Racked robotic tips can be supplied in configurations appropriate to the selected platform and market. Confirm rack footprint, lid, wrapping, sterile state, label, barcode or lot-data needs, case quantity and pallet/carton requirements. Supply planning may include evaluation lots, production batches, annual forecasts and safety stock.

For international orders, provide delivery country, annual or monthly demand and required import or technical documents. Configuration, minimum order quantity and lead time are confirmed during quotation.

Selecting the Correct Tip within the Agilent Bravo Family

Bravo-compatible selection commonly spans 10, 30, 70 and 250 µL families. The 10/30/70 µL groups are commonly associated with high-density workflows, while the 250 µL family is commonly associated with a 96-format rack. Match the family to the installed head rather than capacity alone.

Choose the smallest capacity that comfortably covers the validated transfer range, while matching the installed head and rack format. A protocol spanning substantially different volumes may benefit from more than one tip family.

RFQ Information Checklist

Information to Send Example Why It Helps
Platform and installed head Agilent Bravo Prevents selection by brand name alone
Target transfer range 10 µL Supports capacity and filter-state selection
Rack / carrier 384-format rack Confirms footprint, density and pickup geometry
Liquid characteristics Aqueous, viscous, volatile, foaming, cells or beads Guides geometry and qualification planning
Required options Filter, sterile, conductive, nested or special geometry Defines the exact quotation variant
Commercial details Annual quantity, delivery country and required documents Supports MOQ, lead time and logistics review

A complete RFQ enables Puretest to recommend a specific sellable configuration and reduces sample cycles, especially when multiple rack or filter variants exist under the same nominal capacity.

International, Distributor and OEM Support

Puretest supports laboratories, automation integrators, distributors and private-label buyers serving Europe, North America and other international markets. Programs can cover evaluation samples, annual demand, safety stock, carton configuration, labels, artwork, lot information and shipping documents.

OEM/private-label availability is subject to configuration, minimum order quantity, forecast, artwork and lead-time review. Private labeling does not remove the need for customer-side compatibility and method qualification.

Frequently Asked Questions

Are these original Agilent Bravo tips?

No. They are Puretest-manufactured robotic pipette tips designed for compatibility with specified Agilent Bravo workflows. Puretest is not affiliated with or endorsed by the instrument manufacturer.

Does the 10 µL family name guarantee every transfer point?

No. Usable performance depends on platform, head or channel, filter, internal geometry, liquid class and application. Use the family as a selection starting point and validate critical transfers.

How do I confirm platform compatibility?

Provide the exact instrument, installed head or pod, rack/carrier and current tip reference when available. Test a sample for pickup, sealing, ejection and liquid-handling performance.

Are filtered and sterile versions available?

Availability is configuration-dependent. State filter, sterility, wrapping and required documents in the RFQ so the exact sellable configuration can be confirmed.

Can a filtered tip use the same liquid class as a non-filtered tip?

Do not assume so. A filter changes usable internal space and can affect fluid behavior. Qualify the filtered configuration separately.

Are conductive tips required?

Only when the validated method uses a compatible conductive liquid-level-detection strategy or another requirement specifies conductive material. Confirm hardware and method settings.

Can we receive samples before a production order?

Yes. Sample evaluation is recommended before routine use, particularly for a new method or second-source qualification.

What information speeds up a quotation?

Send platform, installed head or pod, target volumes, liquids, filter, sterility, conductivity, rack, documents, annual quantity and delivery country.

Request a Compatibility Sample, Technical Document or Quotation

Send your Agilent Bravo platform and head configuration, 10 µL requirement, rack format, filter, sterility, conductivity or special-geometry needs, required documents, expected annual quantity and delivery country. Puretest will confirm the closest sellable configuration and sample plan.

Contact Puretest for a sample, technical document or quotation

Trademark notice: Agilent and Bravo are trademarks or registered trademarks of their respective owner. Puretest is not affiliated with or endorsed by the instrument manufacturer. Compatibility references identify intended instrument use only.

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