BeyoChIP™ ChIP Assay Kit (Protein A/G磁珠)即BeyoChIP™ Chromatin Immunoprecipitation (ChIP) Assay Kit with Protein A/G Magnetic Beads,也称染色质免疫沉淀检测试剂盒或ChIP检测试剂盒(蛋白A/G磁珠),用于通过免疫沉淀来沉淀和目标蛋白结合的染色质片段,最后通过PCR或Southern等方法来检测沉淀的染色质片段的...
BeyoChIP™ ChIP Assay Kit (Protein A/G磁珠)即BeyoChIP™ Chromatin Immunoprecipitation (ChIP) Assay Kit with Protein A/G Magnetic Beads,也称染色质免疫沉淀检测试剂盒或ChIP检测试剂盒(蛋白A/G磁珠),用于通过免疫沉淀来沉淀和目标蛋白结合的染色质片段,最后通过PCR或Southern等方法来检测沉淀的染色质片段的...
上海玉博生物科技有限公司 主要致力于“ChIP-Grade Protein G Agarose Beads CST 9007S”的生产销售。多年的“ChIP-Grade Protein G Agarose Beads CST 9007S”生产与销售的经验,与各行业新老用户建立了稳定的合作关系,我公司经营的产品名称深受广大用户信赖。欢迎来电咨
Protein lactylation is derived from lactate. It was first discovered on lysine residues of human histone proteins and was defined as an epigenetic mark that regulates gene expression in diverse biological contexts1. Recently, it was posited as a widespread post-translational modification (PTM) that...
Protein-A-Agarose/Lachssperma-DNA, 2,5 mL Recombinant protein A covalently bound to agarose beads for use in chromatin immunoprecipitations (ChIP assays). Sonicated salmon sperm DNA is included to block non-specific DNA binding sites on agarose beads. Ev
Protein-Protein Interaction Assay—1 μg of S-tagged ctYB-1 immobilized on 10 μl of S-protein-agarose beads was used for each binding reaction. After pre-equilibration in a binding and washing (BW) buffer (20 mm Tris, pH 7.5, 150 mm NaCl, and 0.1% Triton), the ctYB-1 beads were...
Vitronectin is readily adsorbed on to a variety of surfaces and can be extracted most conveniently on a column of glass beads or by affinity chromatography with anti-vitronectin antibody or heparin-agarose. Major difficulties encountered relate to its sensitivity towards proteases and denaturation, and...
碧云天生产的免疫沉淀试剂盒(Protein A+G磁珠法) (Immunoprecipitation Kit with Protein A+G Magnetic Beads)是一种通过高质量的重组Protein A+G磁珠,配合用户自备的特异性抗体,进行目的蛋白免疫沉淀或免疫共沉淀的试剂盒。本产品的免疫沉淀产物,可以用于目的蛋白或其蛋白复合物组分的检测。
protein A/G-agarose beads were washed with serum-free medium. Once we discarded supernatants again, CM was added to beads for 1 h, in rotation at 4 °C. After, the CM were centrifuged at 10,000 × g for 10 min, beads were discarded and CM were filtered through a 0.22 μm fil...
Pre-rinsed protein A/G plus agarose beads (50 μl) was added to each ChIP reaction and incubated for 1 h at 4 °C. The beads were then incubated in 200 μl elution buffer at 65 °C for 20 min to elute immunoprecipitated materials. Real-time PCR was performed using ...