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Recombinant Human PTH1R protein (rFc Tag)

种属

Human

纯度

>90 %, SDS-PAGE

标签

rFc Tag

生物活性

未测试

Cat no : Eg6501

Print datasheet

Synonyms

Parathyroid hormone/parathyroid hormone-related peptide receptor, PFE, PTHR, PTHR1



产品信息

纯度 >90 %, SDS-PAGE
内毒素 <0.1 EU/μg protein, LAL method
生物活性
Not tested
来源 HEK293-derived Human PTH1R protein Asp27-Gly188 (Accession# Q03431) with a rabbit IgG Fc tag at the C-terminus.
基因ID 5745
蛋白编号 Q03431
预测分子量 44.2 kDa
SDS-PAGE 47-65 kDa, reducing (R) conditions
组分 Lyophilized from 0.22 μm filtered solution in PBS, pH 7.4. Normally 5% trehalose and 5% mannitol are added as protectants before lyophilization.
复溶 Briefly centrifuge the tube before opening. Reconstitute at 0.1-0.5 mg/mL in sterile water.
储存条件
It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
  • Until expiry date, -20℃ to -80℃ as lyophilized proteins.
  • 3 months, -20℃ to -80℃ under sterile conditions after reconstitution.
运输条件 The product is shipped at ambient temperature. Upon receipt, store it immediately at the recommended temperature.

背景信息

PTH1R (Parathyroid Hormone 1 Receptor) is a class B1 G protein-coupled receptor (GPCR) that serves as the principal mediator of calcium and phosphate homeostasis by responding to two endogenous peptide ligands—parathyroid hormone (PTH) and parathyroid hormone-related protein (PTHrP). Predominantly expressed in kidney, bone, and breast tissue, PTH1R activation triggers divergent intracellular signaling cascades, including the Gαs-adenylyl cyclase-cAMP-PKA pathway and the Gαq-PLC-PKC axis, thereby regulating renal calcium reabsorption, bone remodeling, and skeletal development. Germline mutations in PTH1R cause contrasting skeletal disorders: constitutively activating mutations lead to Jansen-type metaphyseal chondrodysplasia (hypercalcemia and short stature), while inactivating mutations result in Blomstrand lethal chondrodysplasia. In adult medicine, intermittent PTH1R activation by teriparatide or abaloparatide is exploited pharmacologically to promote bone formation in osteoporosis, underscoring the receptor's dual significance in both physiological mineral ion balance and clinical therapeutics.

参考文献:

1.Alekos, Nathalie S et al. JCI insight vol. 8,6 (2023): e165604. 2.Culhane, Kelly J et al. ACS chemical biology vol. 13,8 (2018): 2347-2358. 3.Shimomura-Kuroki, Junko et al. Odontology vol. 105,2 (2017): 150-154. 4.Kim, Beomchang et al. Experimental and therapeutic medicine vol. 22,6 (2021): 1379. 5.Nampoothiri, Sheela et al. The Journal of clinical endocrinology and metabolism vol. 101,11 (2016): 4283-4289.

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