Biomarker Lens

Common biomarkers

  • Hemoglobin
  • Glucose
  • ALT
  • Apolipoprotein B
  • C-Reactive Protein, Cardiac
  • Ferritin
  • Alb/Creat Ratio, Urine
  • Alkaline Phosphatase
  • FSH
  • T4,Free(Direct)

Biomarkers · Chemical

Chlamydia trachomatisNeisseria gonorrhoeae

Also listed as
Chlamydia trachomatis/Neisseria gonorrhoeae
LOINC codes
31208-2, 41212-2, 44533-8, 47358-7, 47361-1, 47364-5, 47365-2, 50411-8, 50412-6, 59052-1, 44538-7, 47430-4
Tests that measure Chlamydia trachomatisNeisseria gonorrhoeae
Quest Diagnostics 8

Tests

Check the catalog code, specimen, method and preparation for every test that measures Chlamydia trachomatisNeisseria gonorrhoeae. Select up to five tests to compare them side by side.

Quest Diagnostics 8 tests

Panels that include this biomarker

  • Reproductive Donor Female Panel 93307

    9 analytes · Serum · Fasting not stated

    Method and collection
    Method
    Immunoassay (IA) • Nucleic Acid Amplification • Transcription Mediated-Amplification (TMA)
    Collection
    Label the tubes according to your standard operating procedure, making sure that each tube has at least two unique patient identifiers. If transport temperatures will be frozen, centrifuge the lavender-top tube and transfer the plasma into a plastic screw-cap vial. The plastic screw-cap vial (aliquot tube) containing plasma must be labeled with the specimen type (plasma) and at least two unique patient identifiers. Aliquot tubes must be processed and labeled at the original collection site. If aliquot tubes are submitted, do not send the original lavender-top tube. Room temperature stability for raw urine: 24 hours before transfer into Aptima. Urine in Aptima: 30 days. Please note: This test is to be used for the screening of DONORS of human cells, tissues, and cellular and tissue-based products for infectious diseases. For Shipper collection please see detailed instructions in Test Resources.
    Reference notes
    See Laboratory Report
    Quest Diagnostics catalog page

  • Reproductive Donor Female with Reflex to HIV Differentiation 13989

    9 analytes · Serum · Fasting not stated

    Method and collection
    Method
    Immunoassay (IA) • Nucleic Acid Amplification • Transcription Mediated-Amplification (TMA)
    Collection
    Label the tubes according to your standard operating procedure, making sure that each tube has at least two unique patient identifiers. If transport temperatures will be frozen, centrifuge the lavender-top tube and transfer the plasma into a plastic screw-cap vial. The plastic screw-cap vial (aliquot tube) containing plasma must be labeled with the specimen type (plasma) and at least two unique patient identifiers. Aliquot tubes must be processed and labeled at the original collection site. If aliquot tubes are submitted, do not send the original lavender-top tube. Room temperature stability for raw urine: 24 hours before transfer into Aptima. Urine in Aptima: 30 days. Please note: This test is to be used for the screening of DONORS of human cells, tissues, and cellular and tissue-based products for infectious diseases. For shipper collection please see detailed instructions in Test Resources.
    Reference notes
    See Laboratory Report
    Quest Diagnostics catalog page

  • Reproductive Donor Male with Reflex to HIV Differentiation and CMV IgG/IgM 13994

    9 analytes · Serum · Fasting not stated

    Method and collection
    Method
    Immunoassay (IA) • Hemagglutination • Nucleic Acid Amplification • Transcription Mediated-Amplification (TMA)
    Collection
    Label the tubes according to your standard operating procedure, making sure that each tube has at least two unique patient identifiers. If transport temperatures will be frozen, centrifuge the lavender-top tube and transfer the plasma into a plastic screw-cap vial. The plastic screw-cap vial (aliquot tube) containing plasma must be labeled with the specimen type (plasma) and at least two unique patient identifiers. Aliquot tubes must be processed and labeled at the original collection site. If aliquot tubes are submitted, do not send the original lavender-top tube. Room temperature stability for raw urine: 24 hours before transfer into Aptima®. Urine in Aptima®: 30 days. NOTE: Please include serum, red-top (no gel) for CMV portion of testing. Please note: This test is to be used for the screening of DONORS of human cells, tissues, and cellular and tissue-based products for infectious diseases. For Shipper collection please see detailed instructions in Test Resources.
    Reference notes
    See Laboratory Report
    Quest Diagnostics catalog page

  • Reproductive Donor Male with Reflex to HIV Differentiation and CMV IgM 13993

    9 analytes · Serum · Fasting not stated

    Method and collection
    Method
    Immunoassay (IA) • Hemagglutination • Nucleic Acid Amplification • Transcription Mediated-Amplification (TMA)
    Collection
    Label the tubes according to your standard operating procedure, making sure that each tube has at least two unique patient identifiers. If transport temperatures will be frozen, centrifuge the lavender-top tube and transfer the plasma into a plastic screw-cap vial. The plastic screw-cap vial (aliquot tube) containing plasma must be labeled with the specimen type (plasma) and at least two unique patient identifiers. Aliquot tubes must be processed and labeled at the original collection site. If aliquot tubes are submitted, do not send the original lavender-top tube. Room temperature stability for raw urine: 24 hours before transfer into Aptima®. Urine in Aptima®: 30 days. NOTE: Please include serum, red-top (no gel) for CMV portion of testing. Please note: This test is to be used for the screening of DONORS of human cells, tissues, and cellular and tissue-based products for infectious diseases. For Shipper collection please see detailed instructions in Test Resources.
    Reference notes
    See Laboratory Report
    Quest Diagnostics catalog page

  • Reproductive Donor Male with Reflex to CMV IgG/IgM 13991

    10 analytes · Serum · Fasting not stated

    Method and collection
    Method
    Immunoassay (IA) • Hemagglutination • Nucleic Acid Amplification • Transcription Mediated-Amplification (TMA)
    Collection
    Label the tubes according to your standard operating procedure, making sure that each tube has at least two unique patient identifiers. If transport temperatures will be frozen, centrifuge the lavender-top tube and transfer the plasma into a plastic screw-cap vial. The plastic screw-cap vial (aliquot tube) containing plasma must be labeled with the specimen type (plasma) and at least two unique patient identifiers. Aliquot tubes must be processed and labeled at the original collection site. If aliquot tubes are submitted, do not send the original lavender-top tube. Room temperature stability for raw urine: 24 hours before transfer into Aptima. Urine in Aptima: 30 days. NOTE: Please include serum, red-top (no gel) for CMV portion of testing. Please note: This test is to be used for the screening of DONORS of human cells, tissues, and cellular and tissue-based products for infectious diseases. For shipper collection please see detailed instructions in Test Resources.
    Reference notes
    See Laboratory Report
    Quest Diagnostics catalog page

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We compile this page from named laboratory catalogs, guidelines and studies. Labs calculate reference intervals from the people they test, for one assay method and one population group, so an interval describes that population rather than an optimal target.

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