- ￥6552 - 8892
- Biorbyt
- 英国
- orb1837508
- 2026年08月07日
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- 文献和实验
- 技术资料
- 保存条件：
详询
- 保质期：
12 months from date of receipt.
- 英文名：
LACTB2 siRNA (Mouse)
- 库存：
99
- 供应商：
Biorbyt
- 规格：
15 nmol/30 nmol
| 规格： | 15 nmol | 产品价格： | ￥6552.0 |
|---|---|---|---|
| 规格： | 30 nmol | 产品价格： | ￥8892.0 |
描述: siRNA to inhibit LACTB2 expression using RNA interference
别名: Beta-lactamase-like protein 2
形态: Liquid
靶点: LACTB2
适应物种: Mouse
应用: RNA-I
应用说明: Components: We offers pre-designed sets of 3 different target-specific siRNA oligo duplexes of mouse LACTB2 gene. Each vial contains 5 nmol of lyophilized siRNA. The duplexes can be transfected individually or pooled together to achieve knockdown of the target gene, which is most commonly assessed by qPCR or western blot. Directions for Use: We recommends transfection with 10 nM - 100 nM siRNA 48 to 72 hours prior to cell lysis. Before resuspending, briefly centrifuge the tube to ensure the lyophilized siRNA is at the bottom of the tube. Resuspend the siRNA oligos to an appropriate concentration with DEPC water. For example, resuspend one tube of 5 nmol siRNA oligo in 250 μl of DEPC water to get a final concentration of 20 μM
纯度: > 97%
来源: Synthetic
特异性: LACTB2 siRNA (Mouse) is a target-specific 19-23 nt siRNA oligo duplexes designed to knock down gene expression.
UniProt ID: Q99KR3
Entrez 基因 ID: 0, 212442
保存条件: Shipped at 4 °C. Store at -20 °C for one year.
备注: For research use only.
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文献和实验-designed using the Cenix algorithm from Ambion. Designs are currently available for >98% of the human, mouse, and rat genes in the RefSeq database. See the Pre-designed siRNA Catalog Page for more information. In addition, Ambion offers Silencer Validated
of interest. Alternatively, the Whitehead Institute of Biomedical Research at MIT has a publicly available siRNA design tool that incorporates additional selection parameters and integrates BLAST searches of the human and mouse genome databases. See http://jura
Hydrodynamic Delivery of siRNA in a Mouse Model of Sepsis
The use of siRNA in vivo as well as in animal models has become more widespread in recent years, leading to further questions as to the best mode of delivery that will achieve optimal knockdown. While the exact mechanism of siRNA uptake
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