fPSA Fast Test Kit

fPSA Fast Test Kit

Getein fPSA Fast Test Kit offers fast and quantitative detection of free PSA levels in serum or plasma, aiding the clinical evaluation of prostate disease progression in just 10 minutes.

Description

fPSA Fast Test Kit (Immunofluorescence Assay)

The fPSA Fast Test Kit is a quantitative immunofluorescence assay designed for the detection of free prostate-specific antigen (fPSA) in human serum and plasma. It is primarily used to monitor disease progression or treatment response in patients with prostate conditions and must be used in conjunction with total PSA (tPSA) testing for improved clinical accuracy.

Key Advantages

  • Rapid Results: Quantitative results in just 10 minutes
  • Diagnostic Support: Used alongside tPSA to help distinguish prostate cancer from benign conditions
  • Sample Compatibility: Suitable for serum and plasma testing
  • Enhanced Specificity: fPSA/tPSA ratio improves accuracy in the 4–10 ng/mL “gray zone”
  • Stable Storage: 4–30°C with 24-month shelf life

About fPSA

Free prostate-specific antigen (fPSA) is one form of PSA circulating in the blood. Lower fPSA levels are typically associated with prostate cancer, whereas higher levels are more often seen in benign prostatic hyperplasia (BPH). The fPSA/tPSA ratio is a critical tool in evaluating prostate health in men aged 50+ with borderline PSA levels. This test should not be used alone for cancer screening or early detection.

Specifications

Parameter Details
Test Item fPSA (Free PSA)
Sample Type Serum, Plasma
Detection Method Immunofluorescence Assay
Detection Range 0.05–30.00 ng/mL
Cut-off Value 1.00 ng/mL
Test Time 10 Minutes
Storage Conditions 4–30°C
Shelf Life 24 Months

Compatible Devices

  • Getein 1100 Immunofluorescence Quantitative Analyzer
  • Getein 1600 Immunofluorescence Quantitative Analyzer

Clinical Applications

  • Monitoring of disease progression in patients with known prostate malignancies
  • Evaluation of treatment response in conjunction with total PSA
  • Not intended for general population screening or early diagnosis