Alpha-1-Antitrypsin Phenotype

Test information: Phenotyping is recommended when A1AT <1.2g/L. A1AT deficiency is an inherited autosomal co-dominant disorder with a incidence of 1 in 2000-5000 individuals. The Z and S alleles are the most frequent deficiency alleles. DO NOT FREEZE PRIOR TO TESTING.

Specimen Type(s)

• Blood;

Other Acceptable Specimen Type(s)

N/A

Specimen Container - Adult

• Gold Top SST BD;

Specimen Container - Paediatric

• Clear - Plain;

Analytes

• N/A;

Part of a test profile?

No

Volume (min) of sample to be sent to laboratory

1ml

Patient Preparation, Sample Handling and Transport

Neonates, if transfused please wait 3-4 weeks. CMV virus can cause false positive results.

Maximum add on time

N/A

Units and Reference Ranges / Interpretation

Phenotype (e.g. PI Z) with an interpretative comment

UKAS number

8494

UKAS accredited test?

Yes

Comments

N/A

If you have any queries about a test or results interpretation please contact us.