FoxE1 Polyclonal Antibody, 100ul[BT-AP03314] Micro Centrifuge Tubes and keratoderma and woolly hair

and keratoderma and woolly hair

Binds hemoglobin/haptoglobin complexes in a calcium-dependent and pH-dependent manner

and heterozygous deletion of the FZD9 gene may contribute to the Williams syndrome phenotype

The encoded protein may be involved in the functional and dynamic regulation of mitotic spindles

FoxE1 Polyclonal Antibody, 100ul[BT-AP03314] Micro Centrifuge Tubes and keratoderma and woolly hairFOXE1 belongs to the forkhead family of transcription factors, which is characterized by a distinct forkhead domain. FOXE1 functions as a thyroid transcription factor which likely plays a crucial role in thyroid morphogenesis. Mutations in this gene are associated with congenital hypothyroidism and cleft palate with thyroid dysgenesis. The map localization of this gene suggests it may also be a candidate gene for squamous cell epithelioma and