功能： disease:Defects in PROP1 are a cause of combined pituitary hormone deficiency (CPHD) [MIM:601538, 262600]. It is characterized by impaired production of growth hormone (GH) and one or more of the other five anterior pituitary hormones.,function:Possibly involved in the ontogenesis of pituitary gonadotropes, as well as somatotropes, lactotropes and caudomedial thyrotropes.,similarity:Belongs to the paired homeobox family.,similarity:Contains 1 homeobox DNA-binding domain.,tissue specificity:Expressed specifically in embryonic pituitary.,
相关产品： RS0001,RS0002,YM3028,YM3029
细胞定位： Nucleus .
组织表达： Expressed specifically in embryonic pituitary.
科研货号： PLA007675
PROP1 Polyclonal Antibody
Catalog NoPLA007675
Product information
基因名称： PROP1
蛋白名称： Homeobox protein prophet of Pit-1 (PROP-1) (Pituitary-specific homeodomain factor)
功能： disease:Defects in PROP1 are a cause of combined pituitary hormone deficiency (CPHD) [MIM:601538, 262600]. It is characterized by impaired production of growth hormone (GH) and one or more of the other five anterior pituitary hormones.,function:Possibly involved in the ontogenesis of pituitary gonadotropes, as well as somatotropes, lactotropes and caudomedial thyrotropes.,similarity:Belongs to the paired homeobox family.,similarity:Contains 1 homeobox DNA-binding domain.,tissue specificity:Expressed specifically in embryonic pituitary.,
相关产品： RS0001,RS0002,YM3028,YM3029
细胞定位： Nucleus .
组织表达： Expressed specifically in embryonic pituitary.
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