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- 详细信息
- 文献和实验
- 技术资料
- 英文名:
Fluorescein-12-dUTP
- 保质期:
见产品外包装
- 供应商:
嵘崴达
- 保存条件:
−20°C
- 库存:
需确认
- 规格:
25 μL
荧光素-12-dUTP
Fluorescein-12-dUTP
Application
Fluorescein-12-dUTP is used as a substrate for:
• terminal transferase
• DNA polymerase I (holoenzyme and Klenow fragment),
• Taq DNA polymerase
• reverse transcriptase (e.g., from AMV and M-MuLV).
Fluorescein-12-dUTP has been used to label nuclear extracts during PCR. It has also been used to replace dTTP in the random-primed DNA labeling reaction or in nick translation reactions, as well as in PCR. The nucleotide also serves as a substrate for terminal transferase in 3′-end labeling and TUNEL. Fluorescein-labeled probes can be used for in in situ hybridization with direct fluorescence detection or detection by enzyme linked immunoimmunsorbent assay (ELISA) using Anti-Fluorescein-AP, Fab fragments. Repeated fluorescence labeling using Tetramethyl-Rhodamine-6-dUTP (red) and AMCA-6-dUTP (bright blue) is possible.
Quality
典型分析:至少85%荧光素-12-dUTP(HPLC,峰面积%)。
Physical form
荧光素-12-dUTP,四锂盐。
Storage and Stability
The unopened reagent is stable at 15 to 25°C until the expiration date printed on the label. Decomposition of approx. 5% may occur within 6 months.
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文献和实验Random Prime Labeling of DNA Probes with Fluorescein-11-dUTP
The selection of an appropriate labeling reagent for a particular experiment, for the most part, depends on the sensitivity and resolution required. For maximum sensitivity in filter hybridizations radioactive labels, such as phosphorous 32
3′-End Labeling of Oligonucleotides with Fluorescein-11-dUTP and Enhanced Chemiluminescent Detection
In this reaction, the enzyme terminal transferase is used to introduce a short tail of fluorescein nucleotides to the 3′-end of an oligonucleotide (1 ) followed by horseradish peroxidase-catalyzed enhanced chemiluminescent detection
phosphatase indoxyl-nitroblue tetrazolium reaction 172 Detection of neuropeptide mRNAs in tissue sections using oligonucleotides tailed with fluorescein-12-dUTP or DIG-dUTP 178 RNA in situ hybridization using DIG-labeled cRNA probes 181 Detection of mRNAs
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