WebCYP17A1 也称细胞色素 P450C17,它是一种属于 P450 细胞色素单氧酶超家族的类固醇激素合成酶 (1, 2)。. 在人体中,CYP17A1 在肾上腺皮质中高表达,并在雄激素合成通路中起到关键作用 (2)。. CYP17A1 是阿比特 … Web胆固醇7α-羟化酶(Cholesterol 7-alpha hydroxylase, CYP7A1)是胆汁酸合成经典途径的限速酶[], 催化胆固醇在肝脏分解为胆汁酸, 属肝脏特异性微粒体细胞色素P450酶系.人体内近50%的胆固醇通过CYP7A1的催化转化为胆汁酸 …
CYP17A1 gene: MedlinePlus Genetics
Web(A) Knockdown of Cyp17a1 specifically in the liver. (B and C) Fasting liver DHEA, blood-glucose, and b-hydroxybutyrate levels in mice fasted for 24 h with and without hepatic knockdown of Cyp17a1. WebCYP11A1 (D8F4F) Rabbit mAb. #14217. 使用 CYP11A1 (D8F4F) Rabbit mAb(绿色)对 NCI-H295R(左,阳性)和 SW-13(右,阴性)细胞进行共聚焦免疫荧光分析。. 肌动蛋白丝用 DyLight ® 554 Phalloidin #13054(红色)标记。. 蓝色伪彩 = DRAQ5 ® #4084(DNA 荧光染料)。. 使用 CYP11A1 (D8F4F) Rabbit mAb ... phone no of state medicaid
CYP11A1 (D8F4F) Rabbit mAb Cell Signaling Technology
WebMar 21, 2024 · CYP17A1 (Cytochrome P450 Family 17 Subfamily A Member 1) is a Protein Coding gene. Diseases associated with CYP17A1 include Adrenal Hyperplasia, Congenital, Due To 17-Alpha-Hydroxylase … WebJul 30, 2024 · Background 17α-Hydroxylase deficiency is a recessively inherited autosomal disease caused by mutations in the CYP17A1 gene. It is a rare disease and accounts for approximately 1% of congenital adrenal cortex hyperplasias. Inhibition of 17α-hydroxylase causes low levels of cortisol and high levels of adrenocorticotropic hormone in the blood … WebBackground: CYP17A1 is involved in the steroidogenesis of dehydroepiandrosterone and androstenedione. CYP17A is a target for the hormonal treatment of prostate cancer (PCa). Objectives: To investigate the role of CYP17A1 as a driver of PCa growth. Materials and methods: We examined the expression of CYP17A1 and of androgen receptors (AR) in … phone no pick n pay in malvern