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- 详细信息
- 询价记录
- 文献和实验
- 技术资料
- 保质期:
1年
- 英文名:
Direct-zol RNA Miniprep & Lysis Tubes
- 库存:
大量
- 供应商:
简石生物
- 保存条件:
常温
HIGHLIGHTS
- RNA from TRIzol in 7 minutes.
- Use ZR BashingBead Lysis Tubes for optimal disruption and homogenization of hard-to-lyse samples in TRIzol.
- Unbiased, total RNA including small/miRNAs (>17 nt). DNase I included.
DESCRIPTION
For unbiased lysis of microbes and/or solid tissue in TRIzol, use the ZR BashingBead Lysis Tubes (select option) for efficient homogenization of hard-to-lyse samples prior to RNA purification with the Direct-zol RNA kit. The Direct-zol RNA kit isolates total RNA (including small/miRNAs) from any sample in TRIzol in just 7 minutes.
ZR BashingBead Lysis Tubes (S6003 for animal/plant tissue, S6012 for microbes, S6014 for microbes in tissue/insects) are 2.0 ml screwcap tubes with high density, fracture resistant, chemically inert, ceramic beads and is used upstream for the disruption of hard-to-lyse samples. Simply collect your sample in TRIzol, transfer the lysate into a Lysis Tube and perform mechanical homogenization (high-speed bench homogenizer adapted for 2.0 ml tubes). Then process the TRIzol lysate with the Direct-zol RNA kit by binding directly to the spin-column, wash and elute. DNA-free, RNA is ready to use for any downstream application such as NGS, RT/qPCR and etc.
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文献和实验Preparation of total RNA from whole blood collected in PAXgene tubes
has been incubated in the PAXgene Blood RNA Tube for a minimum of 2 h at room temperature, in order to achieve complete lysis.Preheat a water bath or heat block (for microcentrifuge tubes) to 55℃, during first spin.We spin at 3750 rpm in a standard table
Preparation of total cellular RNA--提取总RNA方法
1) Harvest 1x105 to 108 cells. Wash 1x w/PBS and freeze in liquid N2 and store @ -70℃2) Resuspend each pellet in 1.5ml lysis buffer (300μl 5x Lysis, 75μl 200mM VR, 1.125ml H2 O3) Incubate on ice 5minutes and spin 20min at 8k at 4℃.4) Add equal
1) 用酸性酚 - 硫氰酸胍 - 氯仿提取纯化组织和细胞中的 RNA 1. 选取从组织细胞或细胞中提取 RNA 的适宜方法 组织 a. 分离组织并立即置于液氮中。 b. 将约 100 mg 冰冻组织含液氮的研钵中,用研棒研磨。研磨过程中可加入液氮使组织保持冰冻状态。 c. 将组织碎末移入含 3 ml 溶液 D 的管中。 D












