ULYSIS™ Alexa Fluor™ Nucleic Acid Labeling Kit
ULYSIS™ Alexa Fluor™ Nucleic Acid Labeling Kit
Invitrogen™

ULYSIS™ Alexa Fluor™ Nucleic Acid Labeling Kit

Achieve unparalleled precision and sensitivity in your fluorescence-based applications from FISH to real-time PCR. With a streamlined, non-enzymatic labeling process and a broad selection of vibrant dyes, ULYSIS kits ensure your nucleic acids are ready for any challenge.
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货号标签或染料激发/发射
U21660Alexa Fluor™ 647650/670 nm
U21654Alexa Fluor™ 594588/615 nm
货号 U21660
价格(CNY)
8,795.00
1 kit
添加至购物车
标签或染料:
Alexa Fluor™ 647
激发/发射:
650/670 nm
价格(CNY)
8,795.00
1 kit
添加至购物车

ULYSIS nucleic acid labeling kits provide a unique method for attaching a fluorescent dye to nucleic acids. The labeling reagent in the kit reacts with the N7 of guanine to form a stable coordination complex, and the reaction is simple and fast - just heat denature DNA (5 minutes), add the label (react for 15 minutes), then purify.

Features include:

  • Labeling reaction complete in as little as 15 minutes
  • Available in several Alexa Fluor dye colors
  • Non-enzymatic labeling—avoids the potential biases and limitations associated with enzymatic labeling methods
  • Flexibility—compatible with a wide range of experimental conditions and protocols
  • High sensitivity—provides strong fluorescence signals, enabling detection of low-abundance targets

Reliable labeling with the Universal Linkage System

This series of ULYSIS kits was developed to enable rapid and simple coupling of Alexa Fluor dyes to purine bases in nucleic acid polymers. The method, the Universal Linkage System (ULS), makes use of a platinum dye complex that forms a stable adduct with the N7 position of guanine and, to a lesser extent, adenine bases in DNA, RNA, PNA, and oligonucleotides. The result is a reliable nonenzymatic method for nucleic acid labeling.

Labeling is fast and easy

The labeling reaction typically takes only 15 minutes, and separation of the labeled nucleic acids from the unreacted ULS complex can be accomplished with a simple spin-column procedure. DNA longer than ∼1,000 base pairs require a 10-minute DNase digestion before labeling, which both optimizes labeling and fragments the probe for efficient hybridization.

仅供科研使用。不可用于诊断程序。

规格
颜色Far-red
激发/发射650/670 nm
适用于(应用)Dot blot, Northern blot, Southern blot, RNA in situ hybridization, DNA in situ hybridization, Multicolor fluorescence in situ hybridization (mFISH), Comparative genome hybridization (CGH), Microarray analysis
包括标签或染料
标记方法直接标记
产品线Alexa Fluor、Ulysis
产品类型核酸标记试剂盒
数量1 Kit
运输条件室温
检测方法荧光
最终产品类型探针(标记 RNA)、探针(标记 DNA)、寡核苷酸(标记)
产品规格试剂盒
标记目标DNA(通用)、寡核苷酸、RNA(通用)
标签或染料Alexa Fluor™ 647
样品类型DNA/RNA
Unit Size1 kit
内容与储存
储存在冰箱中(-5至 -30°C)并避光保存。

需要但不包括:基于凝胶过滤的离心柱,用于从过量标记试剂中纯化标记的 DNA

常见问题解答 (FAQ)

ULYSIS标记是否兼容于基因芯片分析?

是的,已经有许多使用ULYSIS标记探针进行基因芯片分析的例子。这里是一些供您参考的文献:

•Babak T, Zhang W, Marros Q et al. (2004) Probing microRNAs with microarrays: tissue specificity and functional inference. RNA 10(11):1813–1819.
•Hiley SL, Jackman J, Babak T et al. (2005) Detection and discovery of RNA modifications using microarrays. Nucleic Acids Res 33(1):e2.
•Torchet C, Badis G, Devaux F et al. (2005) The complete set of H/ACA snoRNAs that guide rRNA pseudouridylations in Saccharomyces cerevisiae. RNA 11(6):928–938.

可以将ULYSIS核酸标记试剂盒标记的探针保存起来以后使用吗?

ULYSIS标记的探针可以在任意缓冲液、TE、福尔马林、杂交缓冲液或乙醇中长期保存。我们建议使用您的常规存储条件保存探针,只需保持避光。ULYSIS偶联物是非常稳定的。避免苯酚。

对于使用ULYSIS核酸标记试剂盒进行RNA标记,你们有什么诀窍吗?

这里是一个从DNA标记实验方案修改而来的初步实验方案:不要使用核酸酶处理RNA,而是直接在90°C孵育10分钟或在85°C孵育1分钟进行标记。每1μg RNA加入2 μg糖原,然后通过乙醇沉淀进行纯化。请参考以下文献:

•Babak T, Zhang W, Marros Q et al. (2004) Probing microRNAs with microarrays: tissue specificity and functional inference. RNA 10(11):1813–1819.
•Hiley SL, Jackman J, Babak T et al. (2005) Detection and discovery of RNA modifications using microarrays. Nucleic Acids Res 33(1):e2.
•Torchet C, Badis G, Devaux F et al. (2005) The complete set of H/ACA snoRNAs that guide rRNA pseudouridylations in Saccharomyces cerevisiae. RNA 11(6):928–938.

ULYSIS试剂盒可以用来标记长于1000碱基对的探针甚至质粒吗?

用ULYSIS核酸标记试剂盒标记更大的探针是可能的,但是可能需要将染料稀释以避免(或至少减少)聚合现象的发生。请参考这篇文献: Coelho-Castelo AA, Santos Júnior RR, Bonato VL et al. (2003) B-lymphocytes in bone marrow or lymph nodes can take up plasmid DNA after intramuscular delivery. Hum Gene Ther 14(13):1279–1285.

ULYSIS标记的DNA在高温时稳定吗?

使用ULYSIS核酸标记试剂盒标记的寡核苷酸在100°C可以稳定存在5分钟,并且在68°C保存过夜不会引起复合物的解离。

引用和文献 (6)

引用和文献
Abstract
A systematic search for new mammalian noncoding RNAs indicates little conserved intergenic transcription.
Authors:Babak T, Blencowe BJ, Hughes TR
Journal:BMC Genomics
PubMed ID:16083503
'BACKGROUND: Systematic identification and functional characterization of novel types of noncoding (nc)RNA in genomes is more difficult than it is for protein coding mRNAs, since ncRNAs typically do not possess sequence features such as splicing or translation signals, or long open reading frames. Recent "tiling" microarray studies have reported that ... More
A custom microarray platform for analysis of microRNA gene expression.
Authors:Thomson JM, Parker J, Perou CM, Hammond SM
Journal:Nat Methods
PubMed ID:15782152
'MicroRNAs are short, noncoding RNA transcripts that post-transcriptionally regulate gene expression. Several hundred microRNA genes have been identified in Caenorhabditis elegans, Drosophila, plants and mammals. MicroRNAs have been linked to developmental processes in C. elegans, plants and humans and to cell growth and apoptosis in Drosophila. A major impediment in ... More
Expression profile analysis of microRNA (miRNA) in mouse central nervous system using a new miRNA detection system that examines hybridization signals at every step of washing.
Authors:Hohjoh H, Fukushima T
Journal:Gene
PubMed ID:17229533
'MicroRNAs (miRNAs) are small noncoding RNAs, with a length of 19 to 23 nucleotides, which appear to be involved in the regulation of gene expression by inhibiting the translation of messenger RNA. Expression profile analysis of miRNAs is necessary to understand their complex role in the regulation of gene expression ... More
Identification and characterization of bacterial pathogens causing bloodstream infections by DNA microarray.
Authors:Cleven BE, Palka-Santini M, Gielen J, Meembor S, Krönke M, Krut O
Journal:J Clin Microbiol
PubMed ID:16825354
'Bloodstream infections are potentially life-threatening and require rapid identification and antibiotic susceptibility testing of the causative pathogen in order to facilitate specific antimicrobial therapy. We developed a prototype DNA microarray for the identification and characterization of three important bacteremia-causing species: Staphylococcus aureus, Escherichia coli, and Pseudomonas aeruginosa. The array consisted ... More
Probing microRNAs with microarrays: tissue specificity and functional inference.
Authors:Babak T, Zhang W, Morris Q, Blencowe BJ, Hughes TR
Journal:RNA
PubMed ID:15496526
MicroRNAs (miRNAs) are short, stable, noncoding RNAs involved in post-transcriptional gene silencing via hybridization to mRNA. Few have been thoroughly characterized in any species. Here, we describe a method to detect miRNAs using micro-arrays, in which the miRNAs are directly hybridized to the array. We used this method to analyze ... More