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快速内切酶和修饰酶

快速内切酶和修饰酶

DNA 分子量标准

DNA 分子量标准

蛋白提取、纯化及检测

蛋白提取、纯化及检测

ELISA

ELISA

细胞残留检测

细胞残留检测

Blue Plus® Protein Marker (14-100 kDa)

目录号: DM101-02

单 价:¥360

规格:
2×250 µl
250 µl
数量:
-
+
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产品详情介绍

本产品由7种预染蛋白质组成,分子量范围为14 kDa-100 kDa。其中50 kDa为橙色条带,25 kDa、30 kDa、40 kDa、70 kDa、100 kDa为蓝色条带,14 kDa为亮黄色条带,可以动态观察蛋白质电泳状态及清晰地判断蛋白转膜效果。经SDS-PAGE电泳后转移到PVDF或NC膜上可见清晰的彩色条带。橙色条带和亮黄色条带可以方便地判断转膜的方向。    

References

Xia M , Li Z , Chen Y , et al. Protein self-assembly via Zr 4+, ions on spore-based microspheres for immunoassays[J]. Sensors and Actuators B: Chemical, 2018, 254:166-176.

Zhao G , Du L , Xiao W , et al. Induction of protection against divergent H5N1 influenza viruses using a recombinant fusion protein linking influenza M2e to Onchocerca volvulus activation associated protein-1 (ASP-1) adjuvant[J]. Vaccine, 2010, 28(44):0-7240.

Xiankai L , Dongshu W , Huagui W , et al. Curing of Plasmid pXO1 from Bacillus anthracis Using Plasmid Incompatibility[J]. PLoS ONE, 2012, 7(1):e29875.

Xue A , Zhao W W , Liu X , et al. Affinity chromatography of human IgG with octapeptide ligands identified from eleven peptide-ligand candidates[J]. Biochemical Engineering Journal, 2016, 107:18-25. 

Liu Z , Dong X , Song L , et al. Carboxylation of multiwalled carbon nanotube enhanced its biocompatibility with L02 cells through decreased activation of mitochondrial apoptotic pathway[J]. Journal of Biomedical Materials Research Part A, 2014, 102(3):665-673.

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