Recombinant human FGFR2(IIIc) protein (C-6*HIS)
种属
Human
纯度
>90 %, SDS-PAGE
标签
C-6*HIS
生物活性
EC50: 4-17 ng/mL
验证数据展示
产品信息
纯度 | >90 %, SDS-PAGE |
内毒素 | <0.1 EU/μg protein, LAL method |
生物活性 | Immobilized Human FGFR2 (His tag) at 2 μg/mL (100 μL/well) can bind Human FGF1 (rFc tag) with a linear range of 4-17 ng/mL. |
来源 | HEK293-derived Human CD28 protein Arg22-Glu377 (Accession# P21802-1) with a human IgG1 Fc tag at the C-terminus. |
基因ID | 2263 |
蛋白编号 | P21802-1 |
预测分子量 | 40.3 kDa |
SDS-PAGE | |
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.
|
运输条件 | The product is shipped at ambient temperature. Upon receipt, store it immediately at the recommended temperature. |
背景信息
FGFR2 (Fibroblast growth factor receptor 2) is a tyrosine-protein kinase that acts as cell-surface receptor for fibroblast growth factors and plays an essential role in the regulation of cell proliferation, differentiation, migration and apoptosis. Ligand binding leads to the activation of several signaling pathway, such as RAS, MAPK1/ERK2, MAPK3/ERK1 and the MAP Kinase signaling pathway, as well as the AKT1 signaling pathway. Mutations in the gene of FGFR2 are associated with Crouzon syndrome, Pfeiffer syndrome, Craniosynostosis, Apert syndrome, Jackson-Weiss syndrome, Beare-Stevenson cutis gyrata syndrome, Saethre-Chotzen syndrome, and syndromic craniosynostosis.
参考文献:
1.Eswarakumar VP, et al. (2005). Cytokine Growth Factor Rev. 16(2):139-149. 2.Pike, KG. (2017). Topics in Medicinal Chemistry. 8. 3.Azoury SC, et al. (2017). Int J Biol Sci. 13(12):1479-1488.