ICCS 2026 puts therapy-aware flow reagents in focus: CD38(VHH) JK36 and TRBC2
Summary
Beckman Coulter's ICCS 2026 poster programme highlights RUO reagent strategies for difficult interpretation contexts: CD38(VHH) clone JK36 for CD38 detection in the presence of anti-CD38 therapy and TRBC1/TRBC2 conjugates for T-cell clonality research. These are not new product launches.
Source Date
October 4, 2026
Source checked
October 5, 2026
Event Type
ICCS poster evidence / reagent-watch update
Event Date
October 4, 2026
Geography
Global RUO catalogue; ICCS presentation in Miami, USA
Commercial Regulatory Status
CD38(VHH)-Alexa Fluor 488 clone JK36 and TCR Cβ2 (TRBC2)-APC clone SAM.2 are catalogued as Research Use Only. ICCS poster presence does not change regulatory status.
Related CFCM Topics
Reagent Watch; Panel Design; Therapy Interference; Multiple Myeloma; T-cell Clonality; Troubleshooting; Evidence
Category
Reagent
Primary source
Read the source →Facts supported by cited sources
The ICCS poster list includes work on anti-CD38(VHH) conjugates after CD38-directed therapies and on TRBC1/TRBC2 conjugates for T-cell clonality assessment. Current catalogue records identify JK36/C94642 as CD38(VHH)-Alexa Fluor 488, 50 tests, liquid, RUO; and SAM.2/D06177 as TCR Cβ2 (TRBC2)-APC, 50 tests, liquid, RUO.
CFCM explainer
Therapy or clonality question → conventional phenotype can become ambiguous → targeted epitope/clonality reagent may improve interpretability.
Source/credit: CFCM conceptual explainer based on primary product pages and ICCS poster titles. Alt text: therapy-aware reagent decision path.
Claims Requiring Caution
The event page lists poster titles but not sufficient performance data to assess sensitivity, specificity, interference or clinical utility. Beckman's statement that JK36 recognizes an epitope not masked by daratumumab is a manufacturer product claim; RUO status must remain explicit.
Why It Matters
Post-therapy panel design increasingly depends on reagents that remain interpretable after target-directed treatment. JK36 illustrates a therapy-aware reagent strategy: use an analytical epitope intended to remain accessible when conventional anti-CD38 epitopes are occupied. For T-cell clonality, TRBC1/TRBC2 adds another targeted interpretive strategy. CFCM publishes this as WATCH: the reagents and RUO status are verified, while clinical performance and utility require broader independent evidence.
An announcement is not proof of availability or authorisation. Interpret status within the stated jurisdiction and evidence boundary.
Editor and independence disclosure →