Helixyte™ iFluor® 647 Nucleic
Acid Labeling Dye *Optimized for Labeling 2x100 ug DNA/RNA*- ￥7236
- AAT Bioquest
- 美国
- AAT-17963
- 2025年07月09日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
详询
- 保质期：
详询
- 英文名：
Helixyte™ iFluor® 647 Nucleic Acid Labeling Dye *Optimized for Labeling 2x100 ug DNA/RNA*
- 库存：
99
- 供应商：
北京孚博生物
- CAS号：
详询
- 规格：
2Labelings
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文献和实验DNA Probe Purification Protocol
for 2-3 months, but needs heating to redissolve salts in Buffer DP. Non-radioactive labeling reactions usually use higher dNTP concentrations and yield more product thus obviating the need for carrier. 2. Apply the sample to an HiBind™ DNA spin-column
Combined Flow Cytometric Measurement of Two Cell-Surface Antigens and DNA-RNA Content
start to die). Problem: The detection of cellular subpopulations needs improvement. Solution: This protocol was optimized for detection of surface antigens by using low nucleic acid dye concentrations and exchanging 7-AAD
Increasing Sensitivity in Northern Analysis with RNA Probes
to high-stringency hybridizations (probe degradation was actually due to ribonuclease contamination). The inclusion of nonhomologous nucleic acid blocking agents such as total yeast RNA (total yeast RNA is better that tRNA), also contributes
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