Back to Test Catalogue

Venom rVes v 1 (i211) IgE, Serum

Test ID: RVESV1
Orderable by Ontario ND

Test

Method

ImmunoCAP™

Method Description

ImmunoCAP™ assays are based on binding of allergen-specific IgE antibodies in serum to allergen (extract or allergen molecule) coupled in excess to a solid phase. Bound IgE is subsequently detected with enzyme-labeled anti-human IgE, where the fluorescence intensity is proportional to the amount of allergen-specific IgE.

Platform

Phadia

Report Includes

Venom rVes v 1 (i211) IgE

Specimens

Serum

Clinical Utility

This ImmunoCAP Allergen Component test measures IgE antibodies specific to individual molecular allergens. These allergens, which are purified or recombinant proteins, offer the unique opportunity to assess a persons allergic sensitization pattern.

Clinician must determine clinical significance of specific IgE result after correlation with clinical exam and history. Detectable levels are present in patients with allergic disease and in approx. 15% of symptomatic healthy persons. Some with classic atopic symptoms may not have detectable levels. Specific IgE may decrease with time and lack of exposure to allergens.

Test Location

Hamilton General Hospital, 237 Barton St E, Hamilton ON L8L 2X2

Test Version

17-Nov-2023

Specimen

Specimens

Serum

Sample Volume

1 mL

Specimen Comment

Submit enough specimen for number of IgE tests ordered. Each test requires 50 µL and 2 mL is sufficient for 10-12 tests.

Collection & Handling

Handling Information

Store and send frozen.

Additional Information

Stability

Refrigerated 3 days
Frozen 6 Months

Test Version

17-Nov-2023

Performance / Interpretation

Method

ImmunoCAP™

Method Description

ImmunoCAP™ assays are based on binding of allergen-specific IgE antibodies in serum to allergen (extract or allergen molecule) coupled in excess to a solid phase. Bound IgE is subsequently detected with enzyme-labeled anti-human IgE, where the fluorescence intensity is proportional to the amount of allergen-specific IgE.

Platform

Phadia

Turnaround Time

10 days

Results

Name Units Reference Range Conversion Factor
Venom rVes v 1 (i211), IgE KU/L
  • <0.35

Clinician must determine clinical significance of specific IgE result after correlation with clinical exam and history. Detectable levels are present in patients with allergic disease and in approx. 15% of symptomatic healthy persons. Some with classic atopic symptoms may not have detectable levels. Specific IgE may decrease with time and lack of exposure to allergens.
Use caution when interpreting drug, venom and potential anaphylactic allergen results.

Test Location

Hamilton General Hospital, 237 Barton St E, Hamilton ON L8L 2X2

Test Version

17-Nov-2023

Interface / Setup

Test Version

17-Nov-2023