Search
Citations & References (5)
Invitrogen™
Alexa Fluor™ 647 Decapack Set
Alexa Fluor™ 647 Reactive Dye Decapack は、アミノアリル標識法での使用のために最適化されています。反応性色素のシングルユースパッケージは、バルク色素を分注する必要がなく詳細を見る
| 製品番号（カタログ番号） | 数量 |
|---|---|
| A32757 | 1セット |
製品番号（カタログ番号） A32757
価格（JPY）お問い合わせください ›
71,300
Each
数量:
1セット
Alexa Fluor™ 647 Reactive Dye Decapack は、アミノアリル標識法での使用のために最適化されています。反応性色素のシングルユースパッケージは、バルク色素を分注する必要がなく、利便性を提供し、色素の活性を最大限に高めます。特別にパッケージさ™ れた Alexa Fluor 647 色素は、アミノアリル dUTP およびアミノアリル UTP 修飾ヌクレオチドの両方に対応しているほか、市販されているほとんどのアミノアリルベースのラベリングキットにも対応しています。
研究用にのみ使用できます。診断用には使用いただけません。
仕様
標識法間接ラベリング
標識または色素Alexa Fluor色素
製品ラインAlexa Fluor
製品タイプ反応色素
数量1セット
出荷条件室温
Unit SizeEach
組成および保存条件
フリーザー（-5～-30度）に保存し、遮光してください。
引用および参考文献 (5)
引用および参考文献
Abstract
Possible sources of dye-related signal correlation bias in two-color DNA microarray assays.
Journal:Anal Biochem
PubMed ID:15265729
'DNA microarray analyses commonly use two spectrally distinct fluorescent labels to simultaneously compare different mRNA pools. Signal correlation bias currently limits accepted resolution to twofold changes in gene expression. This bias was investigated by (i) examining fluorescence and absorption spectra and changes in relative fluorescence of DNAs labeled with the
Design of recombinant antibody microarrays for complex proteome analysis: choice of sample labeling-tag and solid support.
Journal:Proteomics
PubMed ID:17787036
Antibody-based microarray is a novel technology with great potential within high-throughput proteomics. The process of designing high-performing antibody (protein) microarrays has, however, turned out to be a challenging process. In this study, we have developed further our human recombinant single-chain variable-fragment (scFv) antibody microarray methodology by addressing two crucial technological
Effects of atmospheric ozone on microarray data quality.
Journal:Anal Chem
PubMed ID:14632079
A data anomaly was observed that affected the uniformity and reproducibility of fluorescent signal across DNA microarrays. Results from experimental sets designed to identify potential causes (from microarray production to array scanning) indicated that the anomaly was linked to a batch process; further work allowed us to localize the effect
CpG Island microarray probe sequences derived from a physical library are representative of CpG Islands annotated on the human genome.
Journal:Nucleic Acids Res
PubMed ID:15911630
An effective tool for the global analysis of both DNA methylation status and protein-chromatin interactions is a microarray constructed with sequences containing regulatory elements. One type of array suited for this purpose takes advantage of the strong association between CpG Islands (CGIs) and gene regulatory regions. We have obtained 20,736
Whole-genome DNA microarray analysis of a hyperthermophile and an archaeon: Pyrococcus furiosus grown on carbohydrates or peptides.
Journal:J Bacteriol
PubMed ID:12813088
The first complete-genome DNA microarray was constructed for a hyperthermophile or a nonhalophilic archaeon by using the 2,065 open reading frames (ORFs) that have been annotated in the genome of Pyrococcus furiosus (optimal growth temperature, 100 degrees C). This was used to determine relative transcript levels in cells grown at