Please call Clinical Labs of Hawaii at 808.677.7998 (Option 1) with questions about this test.
Synonyms
VEGF Plasma
Vascular Endothelial Growth Factor ELISA
VEGF
Collect
Lavender (EDTA) or pink (K2EDTA).
Specimen Preparation
Separate plasma from cells ASAP or within 2 hours of collection. Transfer 1 mL plasma to an ARUP Standard Transport Tube. (Min: 0.3 mL)
Stability (from collection to initiation)
After separation from cells: Ambient: 4 hours; Refrigerated: 6 hours; Frozen: 6 months
Unacceptable Conditions
Hemolyzed specimens.
Storage/Transport Temperature
CRITICAL FROZEN. Additional specimens must be submitted when multiple tests are ordered.
Performed
Tue
Reported
1-8 days
Methodology
Quantitative Chemiluminescent Immunoassay
Test Site
ARUP (92660)
Reference Interval
9-86 pg/mL
Interpretive Data
This assay is performed using the QuantiGlo® Chemiluminescent EIA kit. Values obtained with different assay methods or kits cannot be used interchangeably.
This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.
CPT Codes
83520
LOINC
34694-0
Collect
Lavender (EDTA) or pink (K2EDTA).
Specimen Preparation
Separate plasma from cells ASAP or within 2 hours of collection. Transfer 1 mL plasma to an ARUP Standard Transport Tube. (Min: 0.3 mL)
Storage/Transport Temperature
CRITICAL FROZEN. Additional specimens must be submitted when multiple tests are ordered.
Stability (from collection to initiation)
After separation from cells: Ambient: 4 hours; Refrigerated: 6 hours; Frozen: 6 months
Interpretive Data
This assay is performed using the QuantiGlo® Chemiluminescent EIA kit. Values obtained with different assay methods or kits cannot be used interchangeably.
This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.
Please call Clinical Labs of Hawaii at 808.677.7998 (Option 1) with questions about this test.
Synonyms
VEGF Plasma
Vascular Endothelial Growth Factor ELISA
VEGF
Collect
Lavender (EDTA) or pink (K2EDTA).
Specimen Preparation
Separate plasma from cells ASAP or within 2 hours of collection. Transfer 1 mL plasma to an ARUP Standard Transport Tube. (Min: 0.3 mL)
Stability (from collection to initiation)
After separation from cells: Ambient: 4 hours; Refrigerated: 6 hours; Frozen: 6 months
Unacceptable Conditions
Hemolyzed specimens.
Storage/Transport Temperature
CRITICAL FROZEN. Additional specimens must be submitted when multiple tests are ordered.
Performed
Tue
Reported
1-8 days
Methodology
Quantitative Chemiluminescent Immunoassay
Test Site
ARUP (92660)
Reference Interval
9-86 pg/mL
Interpretive Data
This assay is performed using the QuantiGlo® Chemiluminescent EIA kit. Values obtained with different assay methods or kits cannot be used interchangeably.
This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.
CPT Codes
83520
LOINC
34694-0
Collection
Collect
Lavender (EDTA) or pink (K2EDTA).
Specimen Preparation
Separate plasma from cells ASAP or within 2 hours of collection. Transfer 1 mL plasma to an ARUP Standard Transport Tube. (Min: 0.3 mL)
Storage/Transport Temperature
CRITICAL FROZEN. Additional specimens must be submitted when multiple tests are ordered.
Stability (from collection to initiation)
After separation from cells: Ambient: 4 hours; Refrigerated: 6 hours; Frozen: 6 months
Interpretive Data
This assay is performed using the QuantiGlo® Chemiluminescent EIA kit. Values obtained with different assay methods or kits cannot be used interchangeably.
This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.
