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50 µg
蛋白名称:uPAR/PLAUR蛋白, uPAR/PLAUR protein
蛋白构建:A DNA sequence encoding the extracellular domain of mouse PLAUR (NP_035243.1) precursor (Met 1-Thr 297) was expressed, fused with a polyhistidine tag at the C-terminus.
表达宿主:HEK293 Cells
蛋白纯度:> 97 % as determined by SDS-PAGE
蛋白活性:Measured by its ability to bind with uPA-His (Cat:10815-H08H) in a functional ELISA.
蛋白内毒素:< 1.0 EU per μg of the protein as determined by the LAL method
预测N端:Leu 24
蛋白分子量:The recombinant mouse PLAUR comprises 285 amino acids and has a predicted molecular mass of 31.4 kDa. In SDS-PAGE under reducing conditions, the apparent molecular mass of rmPLAUR is approximately 50-60 kDa due to glycosylation.
蛋白NP号:NP_035243.1
蛋白氨基酸序列:Met1-Thr297
蛋白标签:C-His
蛋白保存条件:Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
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文献和实验人尿激酶型纤溶酶原激活物受体(PLAUR/uPAR) 酶联免疫分析( ELISA ) 试剂盒使用说明书 本试剂仅供研究使用 目的:本试剂盒用于测定人血清,细胞上清及相关液体样本中尿激酶型纤溶酶原激活物受体(PLAUR/uPAR) 的 含量。 实验原理: 本试剂盒应用双抗体夹心法测定标本中 人尿激酶型纤溶酶原激活物受体( PLAUR/uPAR) 水平。用纯化的 人尿激酶型纤溶
Using the scan‐x Web Site to Predict Protein Post‐Translational Modifications
spectrometry data is providing evidence that almost every protein in the cell undergoes some form of post?translational modification. We describe a protocol to use the scan?x Web site to view predicted acetylation sites in the human proteome and predicted
注意的是,两种配体的洗脱和再生buffer稍有差别,使用的时候还需注意! 系统特点 高达 pM 范围的亲和力(KD up to 6.2 x 10-11 M) 纯化树脂材质稳定 小标签 (8-28 aa)无需移除,不影响蛋白折叠和功能 极高的蛋白纯度(纯度>95%) 应用于多种目标蛋白检测系统:Western blot, ELISA, 免疫荧光, FACS等 兼容多种缓冲条件:高盐,洗涤剂,金属离子,螯合剂,还原剂 适用于多种蛋白的纯化 Twin-Strep-tag®标签蛋白固定在界面上时 (SPR
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