Webinars and Sponsored Roundtables — Register Now

Tuesday, April 28, 2026, 12:00 PM–1:00 PM ET
Discover how next-day comprehensive genomic profiling (CGP) is possible with the Oncomine Comprehensive Assay Plus on the Genexus System—delivering both speed and accuracy.

Webinar presenters Jane Bayani, MHSc, PhD, Assistant Professor and Co-Director, Diagnostic Development, Ontario Institute for Cancer Research, Canada, and Nicola Normanno, MD, Scientific Director, IRCCS Romagnolo Institute for the Study of Tumors, Italy, and Morten Grauslund, PhD, Molecular Biologist, Department of Pathology, Rigshospitalet/Copenhagen University Hospital, Copenhagen, Denmark.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

CAP TODAY does not endorse any of the products or services named within. The webinar is made possible by a special educational grant from Thermo Fisher Scientific. For Research Use Only. Not for use in diagnostic applications. 

Thursday, April 30, 2026, 11:00 AM–12:00 PM ET
Hear an expert discuss how Memorial Sloan Kettering Cancer Center (MSKCC) is utilizing
the oncoReveal® Nexus 21-gene panel to redefine turnaround time and actionable insights
in cancer care. Dr. Ewalt shares a perceptive look at the clinical need for rapid, front-line NGS sequencing, and how a unique, purpose built targeted NGS panel (Pillar Biosciences’ oncoReveal Nexus 21 gene Panel) was developed, validated and implemented clinically by Memorial Sloan Kettering Cancer Center (MSK-REACT) to complement their current comprehensive genomic profiling (CGP) approach.

Webinar presenter Mark Ewalt, MD, Associate Medical Director for Laboratory Operations for Diagnostic Molecular Pathology in the Molecular Diagnostics Service, Department of Pathology and Laboratory Medicine, MSKCC.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

CAP TODAY does not endorse any of the products or services named within. The webinar is made possible by a special educational grant from Pillar Biosciences.

Thursday, May 28, 2026, 1:00–2:00 PM ET
This session is designed to improve understanding and application of recent updates to synoptic pathology reporting protocols such as the latest Reporting Template for Reporting Results of Biomarker Testing of Specimens from Patients with Carcinoma of the Breast. These changes reflect evolving clinical guidelines that directly influence diagnostic accuracy and treatment selection in breast cancer care.

Webinar presenters Thaer Khoury, MD, FCAP, Chair, Pathology and Laboratory Medicine, Roswell Park Comprehensive Cancer Cente, and Colin Murphy,  CEO of mTuitive.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

Subspecialties

Interactive Product Guides

Product Spotlight

Beckman Coulter

Access 2

Company

Beckman Coulter

Name of instrument

Access 2

City, State

Brea, CA

Phone

800-526-3821  

Website

https://www.beckmancoulter.com

Type of instrument

immunoassay

Operational type/Model type

continuous random access/benchtop

List price/First year sold in U.S.

—/2001

Targeted hospital bed size/Targeted

—/annual: < 40, 000

Company manufactures instrument

yes (also sold by McKesson, Henry Schein, Medline, Thermo Fisher Scientific)

Other models in this family of analyzers

Unicel DxI 600, Unicel DxI 800

No. of units in clinical use in U.S./Outside U.S. (countries)

Dimensions (H × W × D)/Instrument footprint

19.5 × 39 × 24 in./6.5 sq. ft.

Weight empty/Weight fully loaded

200 lbs./—

No. of different measured assays onboard simultaneously

24 (24 can be run and calibrated at one time)

No. of user-definable (open chemistry) channels

Test throughput per hour/Assay run time

up to 100/13–55 min.

No. of direct ion-selective electrode channels

Detection methods

• Ion-selective electrode

• Basic metabolic panel

• Complete metabolic panel

Typical time delay from ordering stat test until aspiration of sample

Fully automated microplate immunoassay system

no

Methodologies supported

chemiluminescence

Separation methodologies

magnetic particle

Stat time until completion of a ß-hCG test

15 min.

Stat time until completion of a cTn test

17 min.

• Typical time delay from test order to aspiration of sample

36 sec.

Approximate No. of tests per reagent set/Reagent type

50 per pack or 100 per kit/self-contained multiuse

Reagents refrigerated onboard/Reagents ready to use

yes (2ϒ–8ϒC)/yes

Reagent lot tracking/Reagent inventory

yes/yes

Reagent form/Reagents barcoded

liquid chemistry (closed reagent system)/yes

Separate reagent pack for each specimen/for each test run

no/no

Walkaway capability/Walkaway duration

yes/180 min. or 60 specimens

Design of sample-handling system

rack

Uses washable cuvettes/Uses disposable cuvettes

no/yes (can store up to 294 cuvettes)

Min.–max. sample volume that can be aspirated at one time 

5–200 µL

Min. reaction volume/Min. specimen volume/Min. dead volume

varies by assay/varies by assay/80 μL

Dedicated pediatric sample cup

yes (dead volume: 80 μL)

Primary tube sampling

yes

Accommodates most standard tube sizes/Accepts nonstandard tube sizes

yes/no

Pierces caps on primary tubes

no

Protects against probe collision

no

Detects clots/liquid level/short sample

yes/yes/yes

Detection or quantitation for hemolysis, icterus, lipemia, clots

detection for clots; hemolysis, icterus, lipemia not available

Dilutes patient samples onboard/Susceptibility to carryover

yes (can be programmed to perform dilutions prior to analysis)/—

Automatic rerun capability

no

Sample volume can be concentrated to rerun out-of-linear-range low results

no

Analyzer requires dedicated water supply

no

Autocalibration/Multipoint calibration supported

no (calibrants are not stored onboard)/yes (recommended avg. frequency: 28 days)

Typical calibration frequency for ISE/therapeutic drugs/drugs of abuse/general chemistries/immunoassays

—/—/—/—/28 days

Automatic programmable start/Automatic programmable shutdown

no (< 5 min. start-up time)/no

Onboard real-time QC/Onboard software capability to review QC

no/yes

Supports multiple QC lot numbers per analyte

yes

Waste management

automated collection onboard instrument

Sample barcode-reading capability/Autodiscrimination

yes (Interleaved 2 of 5, Codabar, Code 39, Code 128)/no

Lab can control analyzer from remote computer

yes

Instrument can diagnose its own malfunctions

yes (operator intervention required to order parts)

System malfunctions can be diagnosed via remote monitoring

yes

UPS backup power supply

no

Data-management capability/LIS or EHR systems interfaced

onboard/Cerner, Antrim, CCA, Chemware, Dawning Technologies, ADAC, Dynamic Healthcare, Antek, Siemens, McKesson, more

LIS interface provided/Bidirectional interface capability

yes (included in instrument price)/yes (host query)

Modem servicing provided/Service engineer on-site response time

yes/< 24 hrs.

Mean time between failures

1.4 down service calls per year (displays error codes for troubleshooting)

Average scheduled maintenance time by lab personnel

daily: 7 min.; weekly: 12 min.

Maintenance records kept onboard for user/vendor

yes/no

Maintenance training demonstration module onboard

yes

Training included with purchase/Avg. time for basic user training

yes (2 training slots)/2 days (at vendor site)

Advanced operator training/Extra charge for follow-up or advanced training

yes (at vendor site)/—

Warranty provided/Cost of annual service contract (24 h/7 d)

yes (1 year)/—

Distinguishing features (supplied by company)

offers the robustness of a reference laboratory immunoassay analyzer in convenient size of a benchtop system; standardization of results and reagents across all volume segments; reliable benchtop system providing the same high-quality results as the core lab

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