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  Physician's Guide

Technical Bulletins

Written by ARUP's medical directors and added to this list on a bimonthly basis, technical bulletins provide interpretive data regarding newly available tests, including methodologies and clinical significance.

Available Technical Bulletins by Topic:

• 1p and 19q by FISH
• 17-Hydroxyprogesterone Analysis in Serum by LC-MS/MS
• 16S rDNA Organism Identification
• 21-Hydroxylase Antibody
• Achondroplasia Genotyping
• Adiponectin
• Adrenal Steroids Panel
• AFP-L3% in Serum (Includes Total Alpha-Fetoprotein)
• Alpha-1-Antitrypsin Deficiency, Genotyping
• Alpha Thalassemia Detection by PCR
• Alport Syndrome, Adult Type (COL4A5) 3 Mutations
• Angelman Syndrome Methylation
• Anti-MAG and Anti-SGPG, IgM
• Anti-sp 100 and Anti-gp210, IgG
• Antiphospholipid Syndrome (APS) Testing
• Apolipoprotein B Mutation Analysis
• Apolipoprotein E Mutation Analysis for Cardiovascular Risk
• Arsenic Fractionation
• Bartonella DNA Detection by PCR
• BCL-2 JH mbr Translocation
• BCR/ABL1 Kinase Domain Mutation Analysis
• BCR/ABL, t(9;22) Translocastion Assays
• Beta-2-Adrenergic Receptor Gene (ADRB2) Haplotyping
• Beta Globin Sequencing
• Biotinidase (BTD) 5 Mutations
• BK Virus by Real-Time PCR (Quantitative and Qualitative)
• Bordetella pertussis Toxin Antibodies, IgG and IgA by ELISA
• BRAF V600E Mutation Detection
• BRAF V600E Mutation in Thyroid by PCR, Paraffin
• Carbohydrate-Deficient Transferrin (CDT)
• CHOP Gene Rearrangement by FISH
• Chronic Lymphocytic Leukemia
• Chronic Lymphocytic Leukemia Follow Up Phenotyping by Flow Cytometry
• Connexin 26 Sequencing
• Cross-Linked C-Telopeptides in Serum
• Cystic Fibrosis 3199del6
• Cystic Fibrosis Cis-Trans
• Cystic Fibrosis Deletion and Duplication
• Cystic Fibrosis Full-Gene Sequencing
• Cystic Fibrosis Full-Gene Sequencing and Deletion/Duplication
• Cystic Fibrosis Mutation Panel
• Cystic Fibrosis Mutation Panel, Atypical
• Cytochrome P450 2C9 (CYP2C9)
• Cytochrome P450 2C19 (CYP2C19)
• Cytochrome P450 2D6 (CYP2D6) Mutation Analysis
• Cytomegalovirus (CMV) DNA Quantitation by PCR
• Des-γ-Carboxy Prothrombin (DCP) in Serum
• Drugs of Abuse, Identification and Quantification in Meconium
• Drugs of Abuse - Opiates and Related Drugs
• Drugs of Abuse Testing Expanded Publication: Drug Testing Guide for Chronic Pain Management Services
• E2A-PBX1 t(1 19) Translocation by RT-PCR and Fluorescence Monitoring
• Ewing Sarcoma Family of Tumors
• Estradiol and Estrone in Serum by LC-MS-MS
• F-Actin (Smooth Muscle) IgG by Enzyme Immunoassay
• Factor V Leiden (FVL) Mutation Detection
• Febrile Antibodies Panel
• FLT3 Mutation Detection by PCR
• Fragile X DNA Test
• Free Copper (Direct) in Serum Ultrafiltrate
• Free Cortisol and Cortisone in Urine
• Galactosemia, Full Gene Analysis
• Galactosemia Panel
• Gliadin Peptide Antibodies, IgA & IgG
• Genomic (CGH) Microarray Analysis
• Glaucoma (Primary Congenital)- CYP1B1 Sequencing
• Glucose-6-Phosphate Dehydrogenase (G6PD) DNA Mutation
• Hemoglobin S, C and E Genotyping
• HER2 Gene Amplification in Breast Cancer by Monoplex PCR
• Her2 by FISH
• Hereditary Hemorrhagic Telangiectasia (HHT) - Full Gene Analysis
• Hypochondroplasia
• HLA-B27 Genotype
• Human Leptin
• Human Metapneumovirus (hMPV) Detection by DFA
• Human Platelet Antigen DNA
• Huntington Disease (HD)
• Hyaluronic Acid
• IgH-CCND1 by FISH on Formalin-Fixed, Paraffin-Embedded Tissue
• IgA Pemphigus IgA Epithelial Cell Surface Antibodies
• Immunosuppressants by Tandem Mass Spectrometry
• Inflammatory Bowel Disease
• Inhibin B
• Interleukin-1-Receptor-Associated Kinase-4 (IRAK-4)
• Intraepidermal Nerve Fiber Density Analysis
• inv(16) for AML(CBFB-MYH11) by RT-PCR
• JAK2 (V617F) Mutation by PCR
• JAK2 c.1849G-T (V617F) Mutation Quantification by Real-Time PCR
• Jewish Genetic Disease Panel
• Kaposi Sarcoma-Associated Herpesvirus-Human Herpesvirus 8
• Kell Antigen Genotyping (KEL1-KEL2)
• KIT (D816V) Mutation by PCR
• Lipoprotein-Associated Phospholipase A2 (PLACTM)
• Lyme Disease
• Lynch Syndrome
• Macular Degeneration, Age-Related
• Malaria Antibodies, IgG by ELISA
• Maternal Screening, Sequential
• Maternal Serum Screen, First Trimester
• Maternal Serum Screening, Integrated Test
• Maternal Serum Screening, Quadruple
• Medium Chain Acyl-CoA Dehydrogenase (MCAD)
• Methotrexate Sensitivity by Methylenetetrahydrofolate
• Methylenetetrahydrofolate Reductase (MTHFR) Mutation Detection
• Microsatellite Instability
• Microsatellite Instability by Immunohistochemistry
• Mitochondrial Genome Mutation Scanning
• Multiple Myeloma (MM) by FISH
• Multiple Endocrine Neoplasia
• Mutation Detection in Gastrointestinal Stromal Tumors (GISTS)
• Mycobacterium Tuberculosis Complex Speciation
• Mycobacterium tuberculosis IgG Antibody Detection by ELISA
• Neoplastic Mature T-Cell Evaluation by Flow Cytometry
• Neopterin
• Nicotine and Related Compounds in Urine and SerumPlasma
• NPM1 Mutations in Acute Myelogenous Leukemia
• NMR LipoProfile Test
• Norovirus by RT-PCR
• Novel Screening Assay for Celiac Disease and Dermatitis Herpetiformis
• Outer Membrane Proteins (OMP), IgA
• PAX-FKHR Translocations by RT-PCR
• PML-RARa t(15;17) Translocation by RT-PCR
• Prader-Willi Syndrome
• Primary Carnitine Deficiency (SLC22A5) Full Gene Sequencing
• Procollagen Type 1 N-Terminal Propeptide
• Prolactin Macroadenoma
• RH D Genotyping
• Rh Genotyping: Cc and Ee Antigens, Fetal
• Rabies IgG Antibody Detection by ELISA
• Respiratory Virus Mini Panel by RT-PCR
• Rett Syndrome (MECP2)
• S-100B Serum (for Acquired Brain Injury)
• S-100B Serum (for Melanoma)
• Salivary Cortisol
• SMAD4 (MADH4) Full Gene Sequencing
• Schistosoma IgG Antibody Detection by ELISA
• Soluble Mesothelin-Related Peptides (MESOMARK®)
• Specimen Identity Testing
• Squamous Cell Carcinoma Antigen
• Strongyloides Antibody Detection by ELISA
• SYT-SSX t(X;18) Translocations by RT-PCR
• T-Cell Clonality by Flow Cytometry Analysis of TCR V-Beta
• Testing of Mycobacteria, Nocardia, and Other Aerobic Actinomycetes
• Thanatophoric Dysplasia (Types I and II)
• Thyroid Stimulating Hormone Receptor Antibody (TRAb) 3rd Generation
• Toll-Like Receptor Function (TLR) Assay
• Total Coenzyme Q10 by HPLC, Plasma or Serum
• UGT1A1 (TA) n Polymorphisms and Expression of Uridine
• Urine Supersaturation Profile
• UroVysion(TM) FISH
• Vitamin D, 1,25-Dihydroxy and Vitamin D
• Vitamin B1 in Whole Blood by HPLC
• Warfarin Sensitivity by Genotyping
• Yersinia IgG & IgA by Western blot
• ZAP-70 Analysis by Flow Cytometry

Related Information

• ARUP Consult^®—The Physician's Guide to Laboratory Test Selection and Interpretation