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ESTRADIOL, ULTRASENSITIVE LC/MS/MS
0.5 ML SERUM COLLECTED IN A RED-TOP TUBE (NO GEL)
SPECIFY AGE AND SEX ON TEST REQUEST FORM
PLASTIC SCREW-CAP VIAL
ROOM TEMPERATURE: 48 HOURS
REFRIGERATED: 7 DAYS
FROZEN -20 C: 2 YEARS
FROZEN -70 C: 3 YEARS
RECEIVED ROOM TEMPERATURE
SERUM SEPARATOR TUBE (SST)
LIQUID CHROMATOGRAPHY TANDEM MASS SPECTROMETRY (LC/MS/MS)
LABORATORY DEVELOPED TEST (LDT)
THIS TEST WAS DEVELOPED AND ITS ANALYTICAL PERFORMANCE
CHARACTERISTICS HAVE BEEN DETERMINED BY QUEST DIAGNOSTICS
NICHOLS INSTITUTE, SAN JUAN CAPISTRANO, CA. IT HAS NOT BEEN
CLEARED OR APPROVED BY THE FDA. THIS ASSAY HAS BEEN
VALIDATED PURSUANT TO THE CLIA REGULATIONS AND IS USED FOR
QUEST DIAGNOSTICS/NICHOLS SJC
33608 ORTEGA HWY
SAN JUAN CAPISTRANO CA 92675-2042
DIAGNOSTIC APPLICATIONS OF ESTRADIOL ASSAYS INCLUDE
ASSESSMENT OF OVARIAN FUNCTION IN A WIDE VARIETY OF
SITUATIONS (MENSTRUAL DISORDERS, PRECOCIOUS OR DELAYED
PUBERTY, ASSISTED REPRODUCTION PROTOCOLS). FOR MEN,
ESTRADIOL MEASUREMENT MAY BE USEFUL IN THE EVALUATION OF
Reference ranges are provided as general guidance only. To interpret test results use the reference range in the laboratory report.
The CPT codes provided are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.
LOINC assignment is based on a combination of test attributes, including the method used by the performing laboratory. For tests not performed by Quest Diagnostics, codes are assigned by the performing laboratory.
* The tests listed by specialist are a select group of tests offered. For a complete list of Quest Diagnostics tests, please refer to our Directory of Services.