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Biomarkers · Chemical

CD19

Understand what CD19 signals

LOINC codes
108137-1, 19099-1, 19139-5, 31208-2, 32760-1, 33194-2, 38196-2, 49493-0, 55752-0, 92185-8
Commercial laboratory assays
4

We have not added a physiological summary for this biomarker yet. Compare the commercial laboratory assays and population reference ranges below.

Compare commercial laboratory assays for CD19

Check orderable catalog codes, specimen types, fasting requirements, and demographic reference ranges across laboratories.

Chronic Lymphocytic Leukemia (CLL)/Lymphoma Diagnostic Panel

Laboratory
Quest Diagnostics
Test code
17817
Specimen
Blood
Fasting
Not stated
LOINC
108137-1, 19099-1, 19139-5, 31208-2, 32760-1, 33194-2, 38196-2, 49493-0, 55752-0, 92185-8

Laboratory assay overview

To aid in the diagnosis of chronic lymphocytic leukemia or lymphoma. Initial markers evaluated: CD2, CD3, CD4, CD5, CD7, CD8, CD10, CD11c, CD19, CD20, CD23, CD38, CD56, CD64, FMC7, sKappa, sLambda. CD45 is used for gating.

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Quest Diagnostics test directory, test code 17817

Chronic Lymphocytic Leukemia (CLL)/Lymphoma Follow-up Panel

Laboratory
Quest Diagnostics
Test code
17818
Specimen
Blood
Fasting
Not stated
LOINC
108137-1, 19099-1, 19139-5, 31208-2, 32760-1, 33194-2, 38196-2, 49493-0, 55752-0, 92185-8

Laboratory assay overview

To aid in the follow-up diagnosis of chronic lymphocytic leukemia or lymphoma. Initial markers evaluated: CD3, CD4, CD5, CD7, CD8, CD10, CD11c, CD19, CD20, CD23, CD38, HLA-Dr, sKappa, sLambda. CD45 is used for gating.

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See Laboratory Report

Quest Diagnostics test directory, test code 17818

Hairy Cell Leukemia (HCL)/Lymphoma Follow-up Panel

Laboratory
Quest Diagnostics
Test code
17819
Specimen
Blood
Fasting
Not stated
LOINC
108137-1, 19099-1, 19139-5, 31208-2, 32760-1, 33194-2, 38196-2, 49493-0, 55752-0, 92185-8

Laboratory assay overview

To aid in the follow up of a known hairy cell leukemia. Initial markers evaluated: CD11C, CD19, CD20, CD22, CD25, CD103, sKappa, sLambda. CD45 is used for gating.

View complete laboratory reference notes

See Laboratory Report

Quest Diagnostics test directory, test code 17819

Leukemia/Lymphoma Evaluation

Laboratory
Quest Diagnostics
Test code
35080
Specimen
Blood
Fasting
Not stated
LOINC
108137-1, 19099-1, 19139-5, 31208-2, 32760-1, 33194-2, 38196-2, 49493-0, 55752-0, 92185-8

Laboratory assay overview

This panel may be used in the initial evaluation of patients with clinical suspicion of hematologic neoplasms. Immunophenotyping by flow cytometry can aid in the diagnosis and classification of leukemia and lymphoma [1]. Subsequent testing of additional cell surface antigens may be needed to help establish a diagnosis. Leukemias and lymphomas are heterogenous morphologically and clinically. Identification of cell surface markers (T cell, B cell, progenitor, and myeloid markers) by flow cytometry can help assign a cell lineage to neoplastic cells. Accurate immunotyping aids in the diagnosis, classification, and prognosis of hematologic neoplasm and may inform treatment decisions [1]. This immunotyping panel is designed to expedite the evaluation of patients without provisional diagnosis of a certain type of hematologic neoplasm. The results of this panel must be interpreted with cytological, histological, genetic, and clinical findings to generate accurate diagnosis. Additional cell surface markers not included in this panel may be needed to evaluate certain hematologic malignancies (eg, hairy cell leukemia). Because non-viable cells lead to non-specific antibody binding, specimens should be processed as early as possible. The results of this test should be interpreted in the context of pertinent clinical and family history and physical examination findings. Reference 1. Bain BJ, et al. Leukaemia Diagnosis. 5th ed. John Wiley & Sons;2017:69-134.

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See Laboratory Report

Quest Diagnostics test directory, test code 35080

Verify these ranges and sources

We compile every detail above directly from named laboratory directories and published clinical studies. Laboratories calculate standard reference intervals from the statistical distribution of tested populations for a specific assay method and demographic group, rather than setting universal optimal targets.

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