Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Improved panels for clinical immune phenotyping: Utilization of the violet laser.

Cytometry. Part B, Clinical cytometry - 1 Sept 2018

Ryherd Mark, Plassmeyer Matthew, Alexander Connor, Eugenio Ines, Kleschenko Yuliya, Badger Ariel, Gupta Raavi, Alpan Oral, Sønder Søren Ulrik

Abstract excerpt

BACKGROUND: Clinical diagnostic laboratories are subject to numerous regulations imposed by government agencies. Laboratory developed tests for flow cytometry panels are essentially restricted to the use of analyte-specific reagents (ASR) antibodies. With the advances in clinical flow cytometry systems, there is a trend toward the utilization of blue/red/violet laser flow systems and 8 to 10-color panels....

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Antibodies
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Flow Cytometry

Share to Healthy Volunteers

Share to Immunophenotyping

Share to Lasers

Share to Young Adult

Source

Identifiers

PMID: 28493330
DOI: 10.1002/cyto.b.21532

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Improved panels for clinical immune phenotyping: Utilization of the violet laser.PMID 28493330Read ↗

50-color phenotyping of the human immune system with in-depth assessment of T cells and dendritic cellsSemantic proximity Read ↗

OMIP-102: 50-color phenotyping of the human immune system with in-depth assessment of T cells and dendritic cells.Semantic proximity Read ↗

45-Color Full Spectrum Flow Cytometry Panel for Deep Immunophenotyping of the Major Lineages Present in Human Peripheral Blood Mononuclear Cells with Emphasis on the T cell Memory CompartmentSemantic proximity Read ↗

Standardized high-dimensional spectral cytometry protocol and panels for whole blood immune phenotyping in clinical and translational studies.Semantic proximity Read ↗

OMIP ‐109: 45‐color full spectrum flow cytometry panel for deep immunophenotyping of the major lineages present in human peripheral blood mononuclear cells with emphasis on the T cell memory compartmentSemantic proximity Read ↗

Improved flow cytometric method to enumerate residual cells: minimal linear detection limits for platelets, erythrocytes, and leukocytes.Semantic proximity Read ↗

Fluorochrome-dependent specific changes in spectral profiles using different compensation beads or human cells in full spectrum cytometrySemantic proximity Read ↗

Age Distribution of Multiple Functionally Relevant Subsets of CD4+ T Cells in Human Blood Using a Standardized and Validated 14-Color EuroFlow Immune Monitoring Tube.Semantic proximity Read ↗

High-dimensional spectral cytometry panels for whole blood immune phenotypingSemantic proximity Read ↗

Flow cytometry for hematopoietic cells.Semantic proximity Read ↗

Enumeration of major peripheral blood leukocyte populations for multicenter clinical trials using a whole blood phenotyping assay.Semantic proximity Read ↗

The use of intracellular dyes to create a multiplexed flow cytometry-based red blood cell phenotyping assay.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.