Ordering information regarding a Anti-Mitochondrial Antibody (AMA) test for Clinical Diagnostic Laboratories. Mitochondrial M2 Antibody, IgG (ELISA) Ordering Recommendation May be useful in confirming a diagnosis of primary biliary cholangitis. Mnemonic AMA Performed Mon-Sat Methodology Semi-Quantitative Enzyme-Linked Immunosorbent Assay Reported Within 24 hours New York DOH Approval Status This test is New York DOH approved. Specimen Required Patient Preparation: Collect: Serum separator tube. Specimen Preparation: Separate serum from cells ASAP or within 2 hours of collection. Transfer 0.5 mL to a Standard Transport Tube. (Min: 0.3 mL) Storage/Transport Temperature: Refrigerated. Unacceptable Conditions: Plasma. Contaminated, hemolyzed, grossly icteric, or severely lipemic specimens. Remarks: Stability: After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year (avoid repeated freeze/thaw cycles) Reference Interval 20.0 Units or less Negative 20.1-24.9 Units 25.0 Units or greater Equivocal Positive Interpretive Data Anti-mitochondrial antibodies (AMA) are thought to be present in 90-95% of patients with primary biliary cholangitis (PBC). However, the frequency of detected antibodies may be cohort or assay dependent, as lower sensitivities have been reported. Not all PBC patients are positive for AMA; some patients may be positive for SP100 and/or GP210 antibodies. A negative result does not rule out PBC. Compliance Category: FDA Note CPT Code 86381 Components Component Chart Name Mitochondrial (M2) Antibody, IgG Component Test Code 0050065 LOINC 14251-3 Aliases AMA ANTI-MITOCHONDIRAL ANTIBODY ANTIBODIES TO MICROTUBULE ASSOCIATED PROTEIN 2 ANTIMITOCHONDRIAL ANTIBODIES IMMUNOLOGY PROFILE (AMA) MITOCHONDRIAL ANTIBODIES, SERUM

The product page for the Immunochemical Test at Clinical Diagnostic Laboratories. InSure ONE - One Day Fecal Immunochemical Test *The Fecal Immunochemical kit, as well as a prepaid return envelope, will be shipped to you* A simple, non-invasive test that helps you screen for early signs of colon cancer — from the comfort of home. No doctor’s order, no insurance, no hassle. Colon cancer often develops silently, with no symptoms in the early stages. The InSure® ONE FIT test makes it easy to check for hidden blood in your stool, a key early indicator of colorectal disease, so you can take control of your health before problems become serious. This test is quick, clean, and designed for anyone who wants reliable screening without the stress of appointments, referrals, or long waits. A highly sensitive test that detects tiny, invisible traces of blood in your stool — something you can’t see on your own. Uses advanced antibody technology to identify blood from the lower colon. Does not require diet changes, fasting, or multiple stool samples. Helps identify early warning signs of colon cancer, polyps, or gastrointestinal bleeding. Even if you feel completely fine, FIT testing is one of the easiest and most effective ways to stay ahead of colorectal health issues. Why people choose the InSure® ONE FIT test: Simple at-home collection — no mess and no bathroom handling. Only one sample required — done in minutes. No dietary restrictions before completing the test. Great for routine screening or peace of mind between doctor visits. Fast, accurate processing by our CLIA-certified lab. Ideal for adults who prefer private, accessible screening without insurance barriers. Who is this test for? Perfect for individuals who want: A quick annual colorectal cancer screening A private, self-pay option without waiting for a doctor’s appointment Monitoring between colonoscopies (as advised by a physician) A simple way to stay proactive about their health $35.50 Taxes will be calculated at checkout Buy Now

The product page for the Cholesterol Test Panel for Clinical Diagnostic Laboratories. Cholesterol Test Get a complete picture of your heart health with this detailed cholesterol panel: Total Cholesterol – Measures the overall level of cholesterol in your blood. HDL ("Good") Cholesterol – Helps remove bad cholesterol and supports heart health. LDL ("Bad") Cholesterol – High levels may increase your risk for heart disease. Triglycerides – A type of fat in your blood linked to heart risk when elevated. HDL % of Total Cholesterol – Shows the balance between good and total cholesterol. This test helps you understand your cardiovascular risk and supports proactive decisions about your lifestyle and health. $95.00 Taxes will be calculated at checkout Buy Now

The product page for the Men's Fertility Panel for Clinical Diagnostic Laboratories. Men's Fertility Panel This test includes a semen analysis to evaluate key fertility markers such as sperm count, motility (movement), and morphology (shape). It’s a simple, lab-collected test designed to help individuals and couples better understand their reproductive health—whether you're actively trying to conceive or just planning ahead. No insurance, doctor’s order, or copay required. Results are delivered securely within 2–5 business days. Ideal for : Individuals planning for pregnancy Couples facing conception delays Anyone wanting to proactively assess reproductive health $85.00 Taxes will be calculated at checkout Buy Now

Ordering information regarding a Thyroglobulin Antibody test for Clinical Diagnostic Laboratories. Thyroglobulin Antibody Ordering Recommendation Not recommended in the initial evaluation of autoimmune thyroid disease. Most often used to evaluate potentially unreliable thyroglobulin measurements in thyroid carcinomas. Mnemonic ATHYG Performed Mon-Sat Methodology Quantitative Chemiluminescent Immunoassay Reported Within 24 hours New York DOH Approval Status This test is New York DOH approved. Specimen Required Patient Preparation: Collect: Serum separator tube. Specimen Preparation: Transfer 0.5 mL serum to a Standard Transport Tube. (Min: 0.3 mL) Also acceptable: Heparinized plasma. Storage/Transport Temperature: Refrigerated. Unacceptable Conditions: EDTA plasma. Grossly hemolyzed or lipemic specimens. Remarks: Stability: After separation from cells: Ambient: 8 hours; Refrigerated: 1 week; Frozen: 6 months Reference Interval 0.0 - 4.0 IU/mL Interpretive Data A value of 4.0 IU/mL or less indicates a negative result for thyroglobulin antibodies. The Thyroglobulin Antibody assay is being performed using the Beckman Coulter Access Dxl method. Compliance Category: FDA Note CPT Code 86800 Components Component Chart Name Thyroglobulin Antibody Component Test Code 0050105 LOINC 8098-6 Aliases ANTI-THYROGLOBULIN ANTIBODY THYROGLOBULIN ANTIBODY

Ordering information regarding a Myeloperoxidase (MPO) Antibody test for Clinical Diagnostic Laboratories. Myeloperoxidase (MPO) Antibody Ordering Recommendation When used in conjunction with other autoantibody tests (ANCA, PR3), may aid in evaluating suspected immune-mediated vasculitis, especially microscopic polyangiitis (MPA). May be useful to monitor MPA disease and/or treatment response. Panel tests are available. For the workup of suspected vasculitis, refer to ANCA-Associated Vasculitis Profile (ANCA/MPO/PR3) (3003745 ). For patients with a history of vasculitis, refer to Myeloperoxidase (MPO) Antibody and Serine Proteinase 3 (PR3) Antibody with Reflex to Anti-Neutrophil Cytoplasmic Antibody, IgG by IFA (3003746 ). Mnemonic MPO-AB Performed Mon-Sat Methodology Semi-Quantitative Multiplex Bead Assay Reported 1-3 Days New York DOH Approval Status This test is New York DOH approved. Specimen Required Patient Preparation: Collect: Serum separator tube. Specimen Preparation: Separate serum from cells ASAP or within 2 hours of collection. Transfer 1 mL serum to a Standard Transport Tube. (Min: 0.2 mL) Storage/Transport Temperature: Refrigerated. Unacceptable Conditions: Plasma, urine, or other body fluids. Contaminated, hemolyzed, or severely lipemic specimens., icteric, or lipemic specimens. Remarks: Stability: After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year (avoid repeated freeze/thaw cycles) Reference Interval 19 AU/mL or less Negative 20-25 AU/mL 26 AU/mL or greater Equivocal Positive Interpretive Data Approximately 90% of patients with a P-ANCA pattern by IFA have antibodies specific for MPO. Compliance Category: FDA Note CPT Code 83516 Components Component Chart Name Myeloperoxidase (MPO) Ab, IgG Component Test Code 0050526 LOINC 6969-0 Aliases MPO MPO Ab PR3

Ordering information regarding a Cardiolipin Antibody, IgA test for Clinical Diagnostic Laboratories. Cardiolipin Antibody, IgA Ordering Recommendation Preferred second-line test when seronegative antiphospholipid syndrome (APS) is strongly suspected. Order incrementally or concurrently with other noncriteria antiphospholipid antibody tests. Mnemonic CARDIO IGA Performed Mon-Sat Methodology Semi-Quantitative Enzyme-Linked Immunosorbent Assay Reported 1-2 days New York DOH Approval Status This test is New York DOH approved. Specimen Required Patient Preparation: Collect: Serum separator tube. Specimen Preparation: Separate serum from cells ASAP or within 2 hours of collection. Transfer 1 mL serum to a Standard Transport Tube. (Min: 0.3 mL) Storage/Transport Temperature: Refrigerated. Unacceptable Conditions: Plasma or other body fluids. Contaminated, heat-inactivated, hemolyzed, or lipemic specimens. Remarks: Stability: After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year (avoid repeated freeze/thaw cycles) Reference Interval <=12 MPL Negative 13-19 MPL Indeterminate 20-80 MPL Low to Moderately Positive 81 MPL or above High Positive Interpretive Data The persistent presence of IgG and/or IgM cardiolipin (CL) antibodies in moderate or high levels (greater than 40 GPL and/or greater than 40 MPL units) is a laboratory criterion for the diagnosis of antiphospholipid syndrome (APS). Persistence is defined as moderate or high levels of IgG and/or IgM CL antibodies detected in two or more specimens drawn at least 12 weeks apart (J Throm Haemost. 2006;4:295-306). Lower positive levels of IgG and/or IgM CL antibodies (above cutoff but less than 40 GPL and/or less than 40 MPL units) may occur in patients with the clinical symptoms of APS; therefore, the actual significance of these levels is undefined. Results should not be used alone for diagnosis and must be interpreted in light of APS-specific clinical manifestations and/or other criteria phospholipid antibody tests. Compliance Category: FDA Note MPL = IgM phospholipid units CPT Code 86147 Components Component Chart Name Cardiolipin Antibody IgM Component Test Code 0050902 LOINC 3182-3 Aliases ACA aCL aCL Antibody aCL IgG Anti-Cardiolipin Anticardiolipin Anticardiolipin Antibodies Cardiolip

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