CytoSPAR


Develops laboratory technologies for diagnostic and therapeutic products, with a focus on rapid, direct-from-sample phenotypic antimicrobial susceptibility testing using bio-labeling chemistry and fluorescence-based readouts to produce actionable results within a single laboratory shift.

Industries

Biotechnology
Health Care
Medical
Medical Equipment Manufacturing

Nr. of Employees

small (1-50)

CytoSPAR

Easton, Pennsylvania, United States, North America


Products

Direct-from-urine phenotypic AST kit (Research Use Only)

A research-use-only assay kit that uses bio-labeling chemistry and fluorescence readout to assess bacterial viability and determine antimicrobial susceptibility/MIC directly from urine samples.

blAST

blAST is a Bio-Labeled Antimicrobial Susceptibility Test (AST) that uses award-winning click chemistry to analyze antimicrobial sensitivity directly from urine samples, providing single-shift results in approximately 6 hours without requiring a growth phase.


Services

Design and execution support for multisite comparative studies of phenotypic AST methods versus reference standards.

Expertise Areas

  • Phenotypic antimicrobial susceptibility testing
  • Rapid diagnostics for urinary infections
  • Assay development and reagent labeling chemistry
  • Fluorescence-based bioassays and MIC calculation
  • Show More (2)

Key Technologies

  • Click chemistry labeling
  • Fluorescence microplate assays
  • Phenotypic MIC determination
  • Direct-from-sample diagnostic workflows
  • Show More (1)

News & Updates

Poster presenting bacterial labeling method and rapid phenotypic analysis for antibiotic susceptibility testing (ASM Microbe 2024).

Poster reporting detection of antimicrobial resistance using direct-from-sample phenotypic assay (MAD-ID 2026).

Multisite study comparing a direct-from-urine phenotypic antimicrobial susceptibility test with reference broth microdilution methods.

Description of a rapid labeling method that enables phenotypic antimicrobial susceptibility testing via labeled protein synthesis.


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