Skip to main content
Smaller Larger Print

MENU

A  |  B  |  C  |  D  |  E  |  F  |  G  |  H  |  I  |  J  |  K  |  L  |  M  |  N  |  O  |  P  |  Q  |  R  |  S  |  T  |  U  |  V  |  W  |  X  |  Y  |  Z

Tests: C

Test codes, sample requirements and turnaround times for our most requested tests.

Please use the search box below to filter this list

Test name
C-KIT D816V variant by PCR for Mastocytosis
C-MYC IHC
C-Reactive protein (CRP)
C-reactive Protein (CRP) IHC
C1 Esterase gene
C1 Esterase Inhibitor (Antigenic)
C1 Esterase Inhibitor (Functional)
C1 Inhibitor Antibodies
C1q Binding Immune Complex
C2 Gene
C2
C3/C4 Complement
C3 Complement
C3 Nephritic Factor
C3d
C4 Complement
C7 Gene
C8 Gene
CA 125
CA 15-3
CA 19-9
CADASIL – NOTCH3 gene sequencing
Caeruloplasmin
CAKUT (Congenital Anomalies of Kidney & Urinary Tract) NGS Panel – full gene sequencing
Calcitonin
Calcitonin IHC
Calcium
Calculus Analysis
Calponin IHC
Calretinin IHC
Campylobacter serology
Cancer, Comprehensive NGS Panel – full gene sequencing + deletions/duplications
Cancer Antigen 125 (CA125) IHC
Candida Stimulation
CAPD fluid
Carbamazepine
Carbapenemase-producing organism (CPO) screen
Carboxyhaemoglobin
Carbohydrate Antigen 19.9 (CA19.9) IHC
Carbonic Anhydrase IX (CA-IX) IHC
Cardio-Facio-Cutaneous/Noonan/LEOPARD/Costello Syndromes NGS Panel – full gene sequencing
Cardiolipin Antibodies (IgG+IgM)
Cardiomyopathy, Dilated NGS Panel – full gene sequencing + deletions/duplications
Cardiomyopathy, Hypertrophic NGS Panel – full gene sequencing + deletions/duplications
Cardiovascular, Comprehensive NGS Panel – full gene sequencing + deletions/duplications
Carrier Screen (Ashkenazi Jewish) – Partnered Report
Carrier Screen (Ashkenazi Jewish)
Carrier Screen (Pan-Ethnic) – Partnered Report
Carrier Screen (Pan-Ethnic)
Cartilage Antibodies
CASPR2 Antibodies
CCND1 t(11q13) – Lymphoma FISH probe (Breakapart)
CCP Antibodies ([RF])
CD1a IHC
CD2 IHC
CD3 IHC
CD4 IHC
CDK4/CEP12 – Oncology FISH probe (Amplification)
CD5 IHC
CD7 IHC
CD8 IHC
CD10 IHC
CD11c IHC
CD13 IHC
CD14 IHC
CD15 IHC
CD16 IHC
CD19 IHC
CD20/CD21
CD20 IHC
CD21 IHC
CD22 IHC
CD23 IHC
CD25 IHC
CD27 IHC
CD28 IHC
CD30 IHC
CD31 IHC
CD33 IHC
CD34 IHC
CD35 IHC
CD38 IHC
CD40
CD40 IHC
CD40 Ligand (CD154)
CD40L Gene Mutation Analysis
CD43 IHC
CD44 IHC
CD45 IHC
CD45RO IHC
CD52 IHC
CD54 IHC
CD56 (N-CAM) IHC
CD57
CD57 (HNK-1, LEU7) IHC
CD61 IHC
CD68 (KP1) IHC
CD68 (PGM1) IHC
CD71 IHC
CD79a IHC
CD99 IHC
CD103 IHC
CD105 IHC
CD117 (c-KIT) IHC
CD123 IHC
CD138 IHC
CD163 IHC
CD235a (Glycophorin A) IHC
CDX2 IHC
CEA
CEA monoclonal IHC
CEA polyclonal IHC
CENP A Antibodies
CENP B Antibodies
Centromere Autoantibodies
Cerebral Spinal Fluid Morphology (CSF), Pleural Fluid morphology and Ascites Fluid morphology
CGD Proteins p22, gp47, 67, gp91
CH100 (Classical pathway)
Chagas Disease Serology (S.American Trypanosomiasis) T. Cruzi
Charcot-Marie-Tooth Syndrome NGS Panel – full gene sequencing
Charcot-Marie-Tooth Type 1A – PMP22 duplications
CHARGE Syndrome – CHD7 gene sequencing
Chikungunya Virus Abs
Chlamydia (PCR swab)
Chlamydia (Thin Prep)
Chlamydia (Urine)
Chlamydia/Gonorrhoea (PCR Swab)
Chlamydia/Gonorrhoea (Rectal)
Chlamydia/Gonorrhoea (Thin Prep)
Chlamydia/Gonorrhoea (Throat)
Chlamydia/Gonorrhoea (Urine)
Chlamydia/Gonorrhoea/Trichomonas by PCR
Chlamydia Species Specific Antibodies Screen
Chloride
Cholestasis, Intrahepatic NGS Panel – full gene sequencing
Cholesterol
Chromium
Chromogranin A
Chromogranin A IHC
Chromosome Analysis (Amniocentesis) – culture only
Chromosome Analysis (Amniocentesis)– rapid BOBs aneuploidy diagnosis for all chromosomes (5 days) + culture (10-15 days)
Chromosome Analysis (Amniocentesis)– rapid PCR diagnosis for common aneuploidies (2 days) + culture (10-15 days)
Chromosome Analysis (Blood)
Chromosome Analysis (Chorionic Villus) – culture only
Chromosome Analysis (Chorionic Villus)– rapid BOBs aneuploidy diagnosis for all chromosomes (5 days) + culture (10-15 days)
Chromosome Analysis (Chorionic Villus) – rapid PCR diagnosis for common aneuploidies (2 days) + culture (10-15 days)
Chromosome Analysis (Product of Conception) – BOBs rapid aneuploidy diagnosis for all chromosomes (5 days) + culture (25 days)
Chromosome Analysis (Products of Conception)
Chromosome Analysis (Solid Tissue)
Chromosome Analysis (Stem Cells) - Rapid BOBs aneuploidy DNA analysis for all chromosomes (5 days)
Chromosome banding karyotype
Chromosome Y Deletion – AZFa, AZFb, AZFc + SRY
Chronic Leukaemia Screen + MRD
Chymotrypsin IHC
Ciclosporin A
CK-MB
CK5/p63 (Lung) routine double stain IHC
CK5/p63/AMACR (PIN4 - Prostate) routine double stain IHC
CK7/TTF1 (Lung) routine double stain IHC
CLL Genome profile
CLL Prognostification FISH screen
Clostridium difficile Toxin by PCR/EIA (positive)
CMV Chromogenic in situ hybridization (CISH)
CMV DNA by PCR (Guthrie/Dried blood spots)
CMV DNA by PCR (other)
CMV DNA by PCR (Urine)
CMV DNA Quantitation (by PCR)
CMV Resistance
Coagulation Profile 1
Coagulation Profile 2
Cobalt
Coccidioides antibodies
Coeliac Disease – HLA DQ2/DQ8 genotyping
Coeliac/Gluten Profile 2
Coeliac/Gluten Sensitivity Profile
Collagen IV IHC
Colloid Antigen-2 Antibodies
Colorectal Cancer NGS Panel – full gene sequencing + deletions/duplications
Common Gamma Chain
Common Variable Immunodeficiency (CVID) (B-Cells)
Comparative Genomic Hybridisation (Array CGH)
Complement C3
Complement C4
Comprehensive Neuropathy NGS Panel – full gene sequencing
Congenital Absence of Vas Deferens – karyotype + cystic fibrosis screen + polyT(5T) + Y deletions
Congo Red – Special Stain
Conjugated Bilirubin (Direct Bilirubin)
Connective Tissue Disorders/Ehlers-Danlos Syndrome/Aneurysm NGS Panel – full gene sequencing + deletions/duplications
Coombs (Direct Antiglobulin Test)
Copper
Corneal scrapings
Cornelia de Lange Syndrome NGS Panel – full gene sequencing
Coronavirus – COVID-19 IgG Antibody (SARS-CoV-2)
Coronavirus – COVID-19 PCR (SARS-CoV-2)
Cortisol
Costello/Noonan/LEOPARD/Cardio-Facio-Cutaneous Syndromes NGS Panel – full gene sequencing
Coxiella antibodies
Craniosynostosis NGS Panel
Creatine Kinase (Ck)
Creatine Kinase Isoenzymes
Creatinine clearance (Calculated)
Creatinine
Cri du Chat Syndrome – BOBs (5 days) + karyotype (15 days)
Cri du Chat Syndrome – BOBs only
Crithidia Antibodies (dsDNA Abs)
Cryoglobulins
Cryptococcal antigen
CSF for Microscopy and Culture
CSF Glucose
CSF Lactate
CSF PCR
CSF Protein
CSF Screen by PCR (CMV, EBV, HSV, VZV, Enterovirus, Parechovirus)
CSF Xanthochromia
CVS PCR for common aneuploidies (2 days)+ culture (10-15 days)
CVSBOBs only – rapid aneuploidy diagnosis for all chromosomes + common microdeletion syndromes
CVSBOBs – rapid BOBs aneuploidy diagnosis for all chromosomes (3-5 days) + culture (10-15 days)
CXCL-13 IHC
Cyclin A IHC
Cyclin D1 IHC
Cyclin D2 IHC
Cystic Fibrosis (139 common mutations) – reflex to Poly T when CFS required
Cytochrome P450 2C19 (CYP2C19) genotyping
Cytokeratin 5 (CK5) IHC
Cytokeratin 5/p63 (CK5/p63) cocktail IHC
Cytokeratin 7 (CK7) IHC
Cytokeratin 8 (CK8) IHC
Cytokeratin 8/18 (CK18) IHC
Cytokeratin 14 (CK14) IHC
Cytokeratin 17 (CK17) IHC
Cytokeratin 19 (CK19) IHC
Cytokeratin 20 (CK20) IHC
Cytokeratin, High Molecular Weight (34βE12) IHC
Cytokeratin, Low Molecular Weight (CAM 5.2) IHC
Cytokeratin, Pan-cytokeratin (AE1/AE3) IHC
Cytokine Defect Investigations
Cytomegalovirus (CMV-DNA) Amnio
Cytomegalovirus (CMV) IHC
Cytomegalovirus IgG Avidity
Cytomegalovirus (IgG/IgM) Antibodies