PTH elevates calcium level by dissolving the salts in bone and preventing their renal excretion. Stimulates [1-14C]-2-deoxy-D-glucose (2DG) transport and glycogen synthesis in osteoblastic cells.
产品应用
应用
已检合格种属
预测种属
推荐稀释比例
WB
Human
1:1000-2000
IHC-P
Human
1:100-200
IHC-F
Human
1:100-200
IF
Human
1:100-200
交叉反应
交叉反应: Human
相关产品
暂无相关产品
靶标
基因名
PTH
蛋白名
Parathyroid hormone
亚基
Interacts with PTH1R (via N-terminal extracellular domain).
亚细胞定位
Secreted.
疾病
Defects in PTH are a cause of familial isolated hypoparathyroidism (FIH) [MIM:146200]; also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism.
相似性
Belongs to the parathyroid hormone family.
功能
PTH elevates calcium level by dissolving the salts in bone and preventing their renal excretion. Stimulates [1-14C]-2-deoxy-D-glucose (2DG) transport and glycogen synthesis in osteoblastic cells.