此抗体是通过合成与人ISG15蛋白氨基末端氨基酸序列一致的肽段,免疫动物获得,抗体经Protein A和肽亲和层析纯化。 Western blot analysis of lysates from HeLa, A549, RAW and COS cells, treated with or without IFN (1000 U/mL) for 24 hours, using ISG15 antibody. 使用ISG15抗体在经(+)或未经(-)α-干扰素(1000 U / ml)24小时处理的HeLa、A549、RAW和COS等细胞裂解物中检测该蛋白表达的Western blot结果。 Western blot analysis of NEDD8, Ubiquitin, ISG15 and SUMO-2/3 recombinant proteins (5 ng each), using NEDD8 (#2745) , Ubiquitin (#3936), ISG15 (#2743) and SUMO-2/3 (#4974) Antibodies. 分别使用NEDD8 (#2745)、Ubiquitin (#3936)、ISG15 (#2743)和SUMO-2/3 (#4974)抗体对各5ng的NEDD8、泛素、ISG15和SUMO-2/3重组蛋白进行Western blot检测的结果。 Flow cytometric analysis of Hela cells, untreated (blue) or IFNa treated (green), using ISG15 antibody compared to a nonspecific negative control antibody (red). 使用ISG15抗体对未经IFNa处理(蓝色)或经IFNa处理(绿色)的Hela细胞进行流式细胞分析的结果,非特异性阴性抗体检测结果作为对照(红色)。 The relationship between recombinant ISG15 protein concentration and assay optical density readings. Recombinant NEDD8 protein was used as a negative control. 重组ISG15蛋白的浓度和测定的光密度读数之间的关系,重组NEDD8蛋白被用来作为阴性对照。
此抗体是通过合成与人ISG15蛋白氨基末端氨基酸序列一致的肽段,免疫动物获得,抗体经Protein A和肽亲和层析纯化。 Western blot analysis of lysates from HeLa, A549, RAW and COS cells, treated with or without IFN (1000 U/mL) for 24 hours, using ISG15 antibody. 使用ISG15抗体在经(+)或未经(-)α-干扰素(1000 U / ml)24小时处理的HeLa、A549、RAW和COS等细胞裂解物中检测该蛋白表达的Western blot结果。 Western blot analysis of NEDD8, Ubiquitin, ISG15 and SUMO-2/3 recombinant proteins (5 ng each), using NEDD8 (#2745) , Ubiquitin (#3936), ISG15 (#2743) and SUMO-2/3 (#4974) Antibodies. 分别使用NEDD8 (#2745)、Ubiquitin (#3936)、ISG15 (#2743)和SUMO-2/3 (#4974)抗体对各5ng的NEDD8、泛素、ISG15和SUMO-2/3重组蛋白进行Western blot检测的结果。 Flow cytometric analysis of Hela cells, untreated (blue) or IFNa treated (green), using ISG15 antibody compared to a nonspecific negative control antibody (red). 使用ISG15抗体对未经IFNa处理(蓝色)或经IFNa处理(绿色)的Hela细胞进行流式细胞分析的结果,非特异性阴性抗体检测结果作为对照(红色)。 The relationship between recombinant ISG15 protein concentration and assay optical density readings. Recombinant NEDD8 protein was used as a negative control. 重组ISG15蛋白的浓度和测定的光密度读数之间的关系,重组NEDD8蛋白被用来作为阴性对照。