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- 4694279001
- 2025年09月02日
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- 详细信息
- 文献和实验
- 技术资料
- 保质期：
见产品外包装
- 英文名：
Universal ProbeLibrary Probe #141
- 库存：
需确认
- 供应商：
嵘崴达
- CAS号：
见说明书
- 保存条件：
见说明书
- 规格：
1 probe
| packaging | pkg of Probe #141 (04694279001) |
| pkg of Probe #142 (04694287001) | |
| pkg of Probe #143 (04694295001) | |
| pkg of Probe #144 (04694309001) | |
| pkg of Probe #145 (04694317001) | |
| pkg of Probe #146 (04694325001) | |
| pkg of Probe #147 (04694333001) | |
| pkg of Probe #148 (04694341001) | |
| pkg of Probe #149 (04694350001) | |
| pkg of Probe #150 (04694368001) |
General description
Each Universal ProbeLibrary probe is a single hydrolysis probe that recognizes sequences from one or more of the following organisms: humans, chimpanzees and other primates, mice, rats, C. elegans, Drosophila, Arabidopsis.
Short hydrolysis probes for quantification of gene expression levels by real-time PCR.
Application
Use the Universal ProbeLibrary Probes to obtain rapid, flexible quantification of expression levels for virtually any gene from the human, mouse, rat, chimpanzee, C. elegans, Drosophila, or Arabidopsis transcriptomes in the NCBI Reference Sequence Database. Each probe can be used with standard reagents in real-time PCR assays:
• on the LightCycler® Carousel-Based System (e.g., with the LightCycler® TaqMan® Master), or
• on other commercially available real-time PCR instruments (e.g., with the FastStart TaqMan® Probe Master).
Note: You can easily design gene-specific quantification assays using these probes and the free web-based ProbeFinder software at the Assay Design Center.
Features and Benefits
Each of the Universal ProbeLibrary probes:
• Significantly reduces assay design time and implementation time.
• Includes features that make probe-based assays specific, flexible, and convenient.
• Needs no special hardware or unusual reaction conditions.
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文献和实验analysis of genes or regions of interest. ‘Universal’ overgo hybridization probes can be used for the efficient construction of BAC-based physical maps of orthologous chromosome segments from multiple species in parallel. ‘Universal’ overgo hybridization
(see Fig. 1 A ). Friedmann et al. (1 ) first used PCR to screen λgt11 library with two gene-specific primers. This protocol can be effectively used to isolate a particular DNA fragment between two specific primers or to generate nucleic acid probe
Hybridization-based techniques have been extensively employed for the analysis of specific DNA/RNA sequences. Herein, we describe highly specific inexpensive smart hybridization-based sensor that takes advantage of a universal molecular
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