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Test Guide

Search our comprehensive list of tests. Board-certified specialists and pathologists are always a call or email away for expert consulting. We also offer HealthTracks, a dynamic platform that puts all your laboratory results at your fingertips. With HealthTracks, you can easily access detailed reports, provide pet owner-friendly summaries, and manage all your diagnostic needs, all in one convenient place.

Antech Diagnostics Test Guide

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  • Distemper/Parvovirus Vaccine Titers (Canine)

    Test Code
    T565
    Results:
    1-3 days
    Component
    Distemper Virus IgG, Parvovirus IgG
    Specimen
    0.5 mL serum in red top, white top, or serum separator tube
    Test Description
    This test detects IgG antibodies against canine parvovirus and canine distemper virus using ELISA. Results are reported as positive (protective) or negative (insufficient neutralizing antibody detected).This test is not to be used in patient suspected of having distemper or parvovirus infection.

  • Distemper/Parvovirus Vaccine Titers Add-on (Canine)

    Test Code
    ADD270
    Results:
    1-3 days
    Component
    Distemper Virus IgG, Parvovirus IgG
    Specimen
    0.5 mL serum in red top, white top, or serum separator tube
    Test Description
    This is an add-on test code. This test detects IgG antibodies against canine parvovirus and canine distemper virus using ELISA. Results are reported as positive (protective) or negative (insufficient neutralizing antibody detected).This test is not to be used in patient suspected of having distemper or parvovirus infection.

  • Early Detection Chemistry

    Test Code
    SA1002
    Results:
    24 hours
    Component
    TP, ALP, ALT, BUN, CREA, SDMA, CL, GLU, NA, K, NA/K
    Specimen
    0.5 mL serum in red top, white top, or serum separator tube
    Test Description
    A chemistry which includes Alanine Aminotransferase (ALT), Alkaline Phosphatase (ALP), Blood Urea Nitrogen (BUN), Chloride (CL), Creatinine (CREA), Glucose (GLU), Potassium (K), Sodium (NA), Sodium/Potassium Ratio (NA/K), Symmetric dimethylarginine (SDMA), and Total Protein (TP).

  • Early Detection Chemistry, CBC

    Test Code
    SA1004
    Results:
    24 hours
    Component
    Early Detection Chemistry (TP, ALP, ALT, BUN, CREA, SDMA, CL, GLU, NA, K, NA/K), CBC
    Specimen
    0.5 mL serum in red top, white top, or serum separator tube; 1.0 mL whole blood in lavender top tube
    Test Description
    Early Detection Chemistry (SA1002) with Complete Blood Count (CBC).

  • Early Detection Chemistry, CBC, O&P, HWAg

    Test Code
    SA1010
    Results:
    1-2 days
    Component
    Early Detection Chemistry (TP, ALP, ALT, BUN, CREA, SDMA, CL, GLU, NA, K, NA/K), CBC, HWAg, O&P
    Specimen
    0.5 mL serum in red top, white top, or serum separator tube; 1.0 mL whole blood in lavender top tube; 5.0 grams feces in Antech provided fecal container
    Test Description
    Early Detection Chemistry (SA1002) with Complete Blood Count (CBC), Heartworm Antigen (HWAg) detection, and O&P (fecal Ova & Parasites; zinc sulphate centrifugation/floatation).

  • Ehrlichia canis

    Test Code
    T570
    Results:
    1-2 days
    Component
    Ehrlichia canis Ab
    Specimen
    0.5 mL serum in red top, white top, or serum separator tube
    Test Description
    This test detects antibodies (IgG) directed against Ehrlichia canis.

  • Ehrlichia canis Add-on

    Test Code
    ADD05
    Results:
    1-2 days
    Component
    Ehrlichia canis Ab
    Specimen
    0.5 mL serum in red top, white top, or serum separator tube
    Test Description
    This is an add-on test code. This test detects antibodies (IgG) directed against Ehrlichia canis.

  • Ehrlichia/Anaplasma PCR (Canine)

    Test Code
    T980
    Results:
    2-4 days
    Component
    Anaplasma phagocytophilum, Anaplasma platys, Ehrlichia canis, Ehrlichia chaffeensis, Ehrlichia ewingii
    Specimen
    1.0 mL whole blood in lavender top tube, cerebrospinal fluid in lavender top tube, or synovial fluid in lavender top tube
    Test Description
    A highly sensitive and specific PCR panel used to evaluate for evidence of infection by Anaplasma phagocytophilum, Anaplasma platys, Ehrlichia canis, Ehrlichia chaffeensis, and Ehrlichia ewingii.

    A comprehensive PCR panel used when the clinical signs are suggestive of anaplasmosis or erhlichiosis.

  • Ehrlichiosis Serology Panel (Canine)

    Test Code
    S16900
    Results:
    1-7 days
    Component
    Ehrlichia canis, Anaplasma phagocytophilum Ab, Neorickettsia risticii Ab
    Specimen
    2.0 mL serum in red top or serum separator tube
    Test Description
    Evaluates for the presence of antibodies indicating exposure to Ehrlichia canis, Anaplasma phagocytophilum, and Neorickettsia risticii.

  • Electrolyte Screen

    Test Code
    T140
    Results:
    24 hours
    Component
    CL, NA, K, NA/K, bicarbonate, Anion Gap
    Specimen
    0.5 mL serum in red top, white top, or serum separator tube
    Test Description
    Evaluation of Anion Gap, bicarbonate, Chloride (CL), Sodium (NA), Sodium/Potassium Ratio (NA/K), and Potassium (K).

  • Encephalitis Viral Panel Plus (Equine)

    Test Code
    S17500
    Results:
    10-14 days
    Component
    Equine Encephalitis Viral Panel, West Nile Virus Titer (PRNT), West Nile Virus IgM (ELISA), EHV1 Ab
    Specimen
    3.0 mL serum in red top, white top, or serum separator tube
    Test Description
    Equine Encephalitis Viral Panel, West Nile Titer (PRNT & IgM ELISA), and Equine Herpes Virus 1 (EHV1) Ab.

  • Encephalitozoon cuniculi IgG Ab

    Test Code
    S16877
    Results:
    3-5 days
    Component
    Encephalitozoon cuniculi IgG
    Specimen
    0.1 mL serum in red top or white top tube

  • EPM IFAT Panel, Ratio Sarcofluor IFAT, Neofluor IFAT, EPM IFAT Ratio

    Test Code
    S14534
    Results:
    7-10 days
    Component
    Sarcofluor IFAT, Neofluor IFAT, EPM IFAT Ratio
    Specimen
    2.0 mL serum in red top tube or non-additive tube AND 2.0 mL CSF in red top or non-additive tube. Label samples accordingly.
    Submission of serum in serum separator tube is not recommended. Do not use anticoagulant for submission of CSF.
    Test Description
    This test is used to identify intrathecal production of antibody to S. neurona and Neospora hughesi as an indication of active disease within the CNS. This is more accurate for disease than serum testing alone that is only used for exposure.

  • EPM IFAT Panel, Sarcofluor IFAT, Neofluor IFAT

    Test Code
    S14533
    Results:
    7-10 days
    Component
    Sarcofluor IFAT, Neofluor IFAT
    Specimen
    Submit one of the following sample types:
    2.0 mL serum in red top or non-additive tube (submission in serum separator
    tube is not recommended);
    2.0 mL CSF in red top or non-additive tube (do not use anticoagulant).
    Label sample accordingly.
    Test Description
    This tests for exposure to S. neurona and Neospora hughesi as the causative agents of EPM. This test should be interpreted considering seroprevalence of EPM in the area where the horse resides. This test is more likely to be accurate in areas with lower seroprevalence of the disease.

  • EPM SAG 2,4/3 ELISA

    Test Code
    S14388
    Results:
    3-5 days
    Component
    EPM SAG 2,4/3 ELISA
    Specimen
    1.0 mL serum in red top, white top, or serum separator tube OR 1.0 mL CSF in red top tube. Label sample accordingly.
    Test Description
    Detection of the surface antigen proteins 2,4/3 in the serum or Cerebrospinal Fluid (CSF).

    This test identifies exposure to S. neurona and does not confirm active disease. There is no correlation with the level of the titer and the likelihood of disease. A serum to CSF titer ratio is recommended for more definitive diagnosis (see code S14390).

    A negative test result makes EPM an unlikely cause of disease.

  • EPM SAG 2,4/3 ELISA Serum/CSF Ratio

    Test Code
    S14390
    Results:
    3-5 days
    Component
    EPM SAG 2,4/3 ELISA Serum/CSF Ratio
    Specimen
    1.0 mL serum in red top, white top, or serum separator tube AND 1.0 mL CSF in red top tube. Label samples accordingly.
    Test Description
    This test is used to identify intrathecal production of antibody as an indication of active disease within the CNS. The specific antibody index is performed by utilizing a ratio of serum and Cerebrospinal Fluid (CSF) albumin to eliminate the effect of blood crossing into the CNS vs intrathecal antibody production.

  • EPM SAG 2,4/3 ELISA, N. hughesi ELISA

    Test Code
    S14392
    Results:
    3-5 days
    Component
    EPM SAG 2,4/3 ELISA, N. hughesi ELISA
    Specimen
    1.0 mL serum in red top, white top, or serum separator tube OR 1.0 mL CSF in red top tube. Label sample accordingly.
    Test Description
    This tests for exposure of both S. neurona and Neospora hughesi as causative agents for EPM. This is an antibody test for exposure and not confirmation of active disease.

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Test Request Forms

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