跳转至内容
Merck
CN
搜索范围
语言
主题
内容物类型
集合
主题范围
产品分类
应用

255-622-7

应用筛选条件
关键词:'255-622-7'
显示 11-20 #N/A 1286 条结果 关于 "255-622-7" 范围 网站内容
Contact Us
Please contact your local representative for additional help with your order, our products, and product selection.
Scepter™ 3.0 Cell Counter – How it Works
Scepter™ counting is 7 to 10 times faster than hemocytometry-and also faster than other automated counters. Learn more about how this amazing technology works
Enzymatic Assay of Cathepsin B
Cathepsin B is a lysosomal cysteine proteinase with broad specificity. This protocol uses Nα–CBZ–Arg–Arg–7–amido–4–methylcoumarin as the substrate for fluorometric detection of Cathepsin B activity.
In Vitro Differentiation of Human PBMC and CD34+ Derived Monocytes into Mature CD83+/CD14- Dendritic Cells
Generate mature human dendritic immune cells from PBMCs or CD34+ stem cell derived monocytes in 7 days in defined and serum-free dendritic cell culture media. Explore over 350 PromoCell products.
3D Mammosphere Culture Media
3D mammosphere culture protocol used to expand human MCF-7 and MDA-MB-231 breast cancer cells in serum-free/xeno-free stem cell culture media. Explore over 350 PromoCell products on Sigma.com.
基因组DNA样品纯化和质量评估
简单的DNA和RNA纯法方法大幅推动了基因组和基因表达的分析和鉴定。人们需要快速、方便地从多种细胞来源分离DNA和RNA,包括哺乳动物、植物和细菌培养物来源的细胞和组织。
裂解酶
裂解酶提供了一种非机械式细胞裂解和原生质体准备方法。这看上去是个非常简单的过程:只需加入酶,将试管放入水浴然即可。但这过程中到底发生了什么?
植物CRISPR/Cas9基因组编辑
锌指核酸酶(ZFN)是由Sigma-Aldrich在不到8年前推出的,但是从那时起靶向基因组编辑技术已迅速发展。最近,CRISPR/Cas9 通路的发现加快了对该领域的兴趣,为研发开辟了新的可能性。
逆转录
分析基因表达的方法之一是测量基因的mRNA浓度。此类分析面临着若干挑战,例如不同转录本之间的半衰期不同、转录时间模式以及mRNA和蛋白质之间缺乏相关性。
定量PCR基础知识
实时聚合酶链式反应可用于计算样本的起始材料量。它相比常规PCR具有更大的检测动态范围。
2/129