TH Polyclonal Antibody, 20ul[BT-AP08991] High Speed Micro-Centrifuges Mutations in this gene are

Mutations in this gene are believed to result in congenital ocular defects

May function in nuclear protein import as nuclear transport receptor

NF-kappa-B moves to the nucleus and activates transcription of specific genes

CLDN11 encodes a member of the claudin family

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TH Polyclonal Antibody, 20ul[BT-AP08991] High Speed Micro-Centrifuges Mutations in this gene areTyrosine 3 monooxygenase encoded by TH is involved in the conversion of tyrosine to dopamine. It is the rate limiting enzyme in the synthesis of catecholamines, hence plays a key role in the physiology of adrenergic neurons. Mutations in this gene have been associated with autosomal recessive Segawa syndrome. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.