VIM - Overview: Vimentin Immunostain, Technical Component Only

Identification of cells of mesenchymal origin in normal and neoplastic tissues

PAS3 - Overview: Pediatric Allergy Screen <3 Years, Serum

Establishing a diagnosis of an allergy to egg whites, milk, wheat, soybeans, and house dust mites Defining the allergen responsible for eliciting signs and symptoms Identifying allergens: -Responsible for allergic response and/or...

IL5P - Overview: Interleukin 5, Plasma

Evaluation of patients with disorders known to be associated with hypereosinophilia

RALB1 - Overview: Albumin, Random, Urine

Assessing the potential for early onset of nephropathy in diabetic patients using random urine specimens

APHTC - Overview: Amphiphysin Antibody Titer Assay, Spinal Fluid

Evaluating patients with recent onset of a subacute neurological disorder for which a paraneoplastic basis might be suspected, particularly if the patient has a previous history, risk factors, or family history of cancer, especially lung or...

AMMO - Overview: Ammonium, 24 Hour, Urine

Diagnosis of the cause of acidosis Diagnosis and treatment of kidney stones

BARBX - Overview: Barbiturates Confirmation, Chain of Custody, Random, Urine

Detecting drug abuse involving barbiturates such as amobarbital, butalbital, pentobarbital, phenobarbital, and secobarbital Chain of custody is required whenever the results of testing could be used in a court of law. Its purpose is to...

SHRI - Overview: Shrimp, IgE, Serum

Establishing a diagnosis of an allergy to shrimp Defining the allergen responsible for eliciting signs and symptoms Identifying allergens: -Responsible for allergic response and/or anaphylactic episode -To confirm sensitization prior to...

CD273 - Overview: CD273 (PD-L2) Immunostain, Technical Component Only

Differentiation of primary mediastinal large B-cell lymphoma from diffuse large B cell-lymphoma

EM - Overview: Electron Microscopy, Varies

Providing information to aid in the diagnosis of medical disorders such as storage diseases, CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy), and primary ciliary dyskinesia