重组大鼠 IL1R2 / IL1RB / CD121b 蛋白| 参数|技术资料

EDAR蛋白产品信息

别名: RGD1561714
表达方式: A DNA sequence encoding the rat EDAR (NP_001178828.1) extracellular domain (Met 1-Ala 187) was fused with the Fc region of human IgG1 at the C-terminus.
种属: Rat
表达宿主: Human Cells

EDAR Protein QC Testing

纯度: > 95 % as determined by SDS-PAGE SDS-PAGE
内**: < 1.0 EU per μg of the protein as determined by the LAL method
稳定性: Samples are stable for up to twelve months from date of receipt at -70℃
预测N端: Glu 27
分子量: The secreted recombinant rat EDAR/Fc is a disulfide-linked homodimer. The reduced monomer comprises 402 amino acids and predicts a molecular mass of 44.4 kDa. The apparent molecular mass of the ratEDAR/Fc monomer is approximately 60-70 kDa in SDS-PAGE under reducing conditions due to glycosylation.
缓冲液: Lyophilized from sterile PBS, pH7.4.
Normally 5 % - 8 % trehalose and mannitol are added as protectants before lyophilization. Specific concentrations are included in the hardcopy of COA.
Please contact us for any concerns or special requirements.

EDAR Protein Usage Guide

储存方法: Store it under sterile conditions at -70℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
Reconstitution: A hardcopy of COA with reconstitution instruction is sent along with the products. Please refer to it for detailed information.

EDAR蛋白背景综述

Tumor necrosis factor receptor superfamily member EDAR, also known as Anhidrotic ectodysplasin receptor 1, Ectodysplasin-A receptor, Ectodermal dysplasia receptor, Downless homolog, EDAR and DL, is a single-pass type I membrane protein which contains one death domain and three TNFR-Cys repeats. EDAR / DL is a receptor for EDA isoform A1, but not for EDA isoform A2. It mediates the activation of NF-kappa-B and JNK and may promote caspase-independent cell death. EDAR / DL is detected in fetal kidney, lung, skin and cultured neonatal epidermal keratinocytes. It is not detected in lymphoblast and fibroblast cell lines. Defects in EDAR are a cause of ectodermal dysplasia anhidrotic which is characterized by sparse hair (atrichosis or hypotrichosis), abnormal or missing teeth and the inability to sweat due to the absence of sweat glands. Defects in EDAR are also the cause of ectodermal dysplasia type 3 (ED3) which is an autosomal dominant condition characterized by hypotrichosis, abnormal or missing teeth, and hypohidrosis due to the absence of sweat glands.

参考文献

Koppinen P. et al., 2001, Exp Cell Res. 269 (2): 180-92.
Fessing MY. et al., 2006, Am J Pathol. 169 (6): 2075-84.
Drew CF. et al., 2007, Dev Biol. 305 (1): 232-45.
Fujimoto A.et al., 2008, Hum Mol Genet. 17: 835-43.
Kimura R. et al., 2009, Am J Hum Genet. 85 (4): 528-35.

规格：50ug

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