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- Mirusbio
- 美国
- MIR 6003
- 2025年07月16日
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- 保存条件：
Store at -20°C
- 保质期：
/
- 英文名：
TransIT-X2® Dynamic Delivery System
- 库存：
99
- 供应商：
欣博盛生物
- 规格：
0.3 ml
TransIT-X2® Dynamic Delivery System用于在人诱导多能干细胞（iPSC）中转染Cas9蛋白/gRNA核糖核蛋白（RNP）复合物。T7E1错配方法用于测定转染后48小时的切割效率。
| 供应商 | 产品编号 | 产品名称 | 中文产品名称 | 规格 |
| Mirusbio | MIR 6000 | TransIT-X2® Dynamic Delivery System | TransIT-X2® Dynamic Delivery System/适用于DNA、siRNA/miRNA和CRISPR RNP的非脂质体高效低毒转染试剂 | 1.5ml |
| Mirusbio | MIR 6003 | TransIT-X2® Dynamic Delivery System | TransIT-X2® Dynamic Delivery System/适用于DNA、siRNA/miRNA和CRISPR RNP的非脂质体高效低毒转染试剂 | 0.3ml |
| Mirusbio | MIR 6004 | TransIT-X2® Dynamic Delivery System | TransIT-X2® Dynamic Delivery System/适用于DNA、siRNA/miRNA和CRISPR RNP的非脂质体高效低毒转染试剂 | 0.75ml |
| Mirusbio | MIR 6005 | TransIT-X2® Dynamic Delivery System | TransIT-X2® Dynamic Delivery System/适用于DNA、siRNA/miRNA和CRISPR RNP的非脂质体高效低毒转染试剂 | 5x1.5ml |
| Mirusbio | MIR 6006 | TransIT-X2® Dynamic Delivery System | TransIT-X2® Dynamic Delivery System/适用于DNA、siRNA/miRNA和CRISPR RNP的非脂质体高效低毒转染试剂 | 10x1.5ml |
| Mirusbio | MIR 6010 | TransIT-X2® Dynamic Delivery System | TransIT-X2® Dynamic Delivery System/适用于DNA、siRNA/miRNA和CRISPR RNP的非脂质体高效低毒转染试剂 | 0.1ml |
关于Mirusbio公司：Mirus被公认为是核酸研究试剂开发的领跑者，其许多杰出成就受到世界公认：首先研发出siRNA转染试剂；世界上最早开发高效、低细胞毒性转染试剂的公司之一；首先向市场推出“一步法”核酸标记技术；独特的小分子RNA如microRNA标记技术。
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文献和实验PEGPEI Copolymers for Oligonucleotide Delivery to Cells and Tissues
compounds that markedly improve the in vitro and in vivo delivery of AOs to cells and tissues. By varying the Mw of PEI, as well as the nature of PEG shielding, PEG-PEI-AO nanoparticulates can be prepared with a dynamic range of size, surface charge
Lipid-Based Nanoparticles as Nonviral Gene Delivery Vectors
Efficient delivery of nucleic acids into cells is a promising technique to modulate cellular gene expression for therapeutic and research applications. Cationic lipid-based liposomes represent one of the most intensively studied and employed
as well as dynamic light scattering to the structural analysis of the oligonucleotide component of nonviral gene delivery vectors. We also illustrate this approach for the investigation of the formulation of lipoplex and polyplex-based gene delivery systems
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