Involvement in diseaseNote=An alternative splicing in the thyroperoxidase mRNA can cause Graves' disease. Defects in TPO are the cause of congenital hypothyroidism due to dyshormonogenesis type 2A (CHDH2A) [MIM:274500]; also called genetic defect in thyroid hormonogenesis 2A or thyroid hormone organification defect II. CHDH2A is due to defective conversion of accumulated iodide to organically bound iodine. The iodide organification defect can be partial or complete.
Sequence similaritiesBelongs to the peroxidase family. XPO subfamily. Contains 1 EGF-like domain. Contains 1 Sushi (CCP/SCR) domain.
Post-translational modificationsGlycosylated. Heme is covalently bound through a H(2)O(2)-dependent autocatalytic process. Heme insertion is important for the delivery of protein at the cell surface. Cleaved in its N-terminal part.
ab123805 (5µg/ml) staining of paraffin embedded Human Thyroid Gland following steamed antigen retrieval with citrate buffer pH 6 and AP-staining shows textured staining in the cytoplasm of epithelial cells.
Western blot - Anti-Thyroid Peroxidase antibody (ab123805)
Anti-Thyroid Peroxidase antibody (ab123805) at 0.1 µg/ml + Thyroid Gland lysate (in RIPA buffer) at 35 µg developed using the ECL technique
Predicted band size : 103 kDa
References for Anti-Thyroid Peroxidase antibody (ab123805)
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