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Tests: P

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

Please use the search box below to filter this list

Test name
P. jirovecii PCR (BAL, Sputum)
p16 IHC
p16 IHC (Reported)
p27 IHC
p40 IHC
p53 (DO7) IHC
p57 IHC
p53-related cancer predisposition (Li-Fraumeni Syndrome) – TP53 sequencing + MLPA
p63 IHC
PAI1 4G/5G Polymorphism
Pan-TRK IHC (reported)
Pancreatic Cancer NGS Panel – full gene sequencing + deletions/duplications
Pancreatic Islet Cell Antibodies
Pancreatic polypeptide (PPP) IHC
Parathyroid Hormone (PTH) IHC
Paracetamol (Acetaminophen)
Paraganglioma/Pheochromocytoma NGS Panel – full gene sequencing + deletions/duplications
Parathyroid Antibodies
Parathyroid Hormone (PTH)
Parvovirus Antibodies (IgM)
Parvovirus B19 IHC
Parvovirus IgG Antibodies
Parvovirus Quantitative DNA by PCR
Paternity Testing (postnatal and prenatal) – sample required from each person being tested (3 people)
Paul Bunnell (Monospot)
Pax-2 IHC
Pax-5 IHC
Pax-8 IHC
PD-L1 (22C3) IHC
PD-L1 (28-8) IHC
PD-L1 (SP142) IHC
PD-L1 (SP263) IHC
PD1 IHC
PDGFB Breakapart – Oncology FISH probe (Translocation/Rearrangement)
PDGRF Antibodies
Pelizaeus-Merzbacher Disease – PLP1 sequencing + deletions/duplications
Pemphigus/Pemphigoid Autoantibodies
Pendred Syndrome – SLC26A4 gene sequencing
Perforin
Perforin IHC
Periodic Acid Schiff (PAS) – Special Stain
Periodic Acid Schiff, Diastase (DPAS) – Special Stain
Periodic Fever/Autoinflammation NGS Panel – full gene sequencing
Perl’s Prussian Blue – Special Stain
Peutz-Jegher Syndrome – STK11 sequencing + deletions/duplications
PGP9.5 IHC
Phagocytosis Assay
Phelan-McDermid Syndrome – karyotype + FISH
Phenytoin
Pheochromocytoma/Paraganglioma NGS Panel – full gene sequencing + deletions/duplications
Phosphate
Phosphatidylserine Antibodies
Phospholipase A2 Receptor
Phosphotungstic Acid Haematoxylin – Special Stain
Pigmentation/Oculocutaneous Albinism/Hermansky-Pudlak Syndrome NGS Panel – full gene sequencing
Pituitary Antibodies
PL-12 Antibodies
PL-7 Antibodies
PLAP IHC
Plasma Viscosity
Platelet Aggregation Studies
Platelet Antibodies
Platelet function assay (PFA-100 assay)
PM-Scl100 Antibodies
PM-Scl75 Antibodies
PML Antibodies
Pneumococcal Antibodies – Serotype Specific
Pneumococcal Antibody (PCP)
Pneumococcal Urinary Antigen
PNH
PNP (Nucleotide Metabolism)
Podoplanin (D2-40) IHC
POLG-Related Disorders – full POLG sequencing + copy number variant
Polio Virus 1, 2, 3 Antibodies
Polycystic Kidney/NGS Panel – full gene sequencing
Pontocerebellar Hypoplasia NGS Panel – full gene sequencing
Postnatal array CGH
Potassium
Prader-Willi Syndrome (Primary Screen) – methylation PCR
PRAME IHC
Pre-Travel Screen (DVT)
Pregnancy associated plasma protein-A (PAPPA)
Prenatal array CGH
Prenatal Diagnosis (BOBs + Culture)
Prenatal Diagnosis for haemoglobinopathies
PRF1 (perforin) gene and MUNC 13-4 mutation analysis
Primary Ciliary Dyskinesia (PCD) NGS Panel – full gene sequencing
Primary Hyperoxaluria metabolites (glycolate, glycerate, dihydroxyglutarate)
Primary Hyperoxaluria Panel – full gene sequencing + CNV
Procalcitonin
Product of Conception BOBs only – rapid aneuploidy diagnosis for all chromosomes
Product of Conception – rapid BOBs aneuploidy diagnosis for all chromosomes (5 days) + culture (25 days)
Progesterone
Progesterone receptor (16) IHC
Progesterone receptor (16) IHC (Reported)
Prolactin
Prolactin IHC
Proliferation Assay
Prosigna Breast Cancer Assay
Prostate Cancer NGS Panel – full gene sequencing + deletions/duplications
Prostate Specific Acid Phosphatase (PSAP) IHC
Prostate Specific Antigen (PSA)
Prostate Specific Antigen (PSA) IHC
Prostate Specific Membrane Antigen (PSMA) IHC
Prostatitis Screening Panel
Protein C
Prostein (P501S) IHC
Protein Electrophoresis
Protein S Free Ag
Proteinase 3 Antibodies
Prothrombin Time + Dose
Prothrombin Time
PTEN-related disorders (including Bannayan-Riley-Ruvalcaba, Cowden & Proteus Syndromes) – sequencing + deletions/duplications
PTEN IHC
Purkinje Cell Antibodies (Hu and Yo)
PVL toxin gene PCR
Pyruvate Kinase