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Invitrogen™

Alexa Fluor™ 647-aha-dCTP

™ ヌクレオチドの標識に使用™™される Alexa Fluor 647 色素は、一般的に使用されるマイクロアレイスキャナーと互換性があり、標準的に類似した Cy 3詳細を見る
製品番号(カタログ番号)数量
A3277150 μL
製品番号(カタログ番号) A32771
価格(JPY)
95,300
온라인 행사
Ends: 26-Jun-2026
158,900
割引額 63,600 (40%)
Each
数量:
50 μL
™ ヌクレオチドの標識に使用™™される Alexa Fluor 647 色素は、一般的に使用されるマイクロアレイスキャナーと互換性があり、標準的に類似した Cy 3 および Cy 5 色素ペアよりも優れたシグナル相関( R2)値を提供し、2 色マイクロアレイ遺伝子発現アッセイの分解能を 1.3 倍の発現変化に向上させます。非常に明るく光安定性の高い Alexa Fluor™ 色素も、本質的には TOB pH に影響を受けず、水溶性が高くなります。
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
アッセイマイクロアレイ遺伝子発現アッセイ
濃度1 mM
標識法直接標識
標識または色素Alexa Fluor色素
修飾AHA( 5- アミノヘキシルアクリルアミド)
製品ラインAlexa Fluor
製品タイプ標識ヌクレオチド
数量50 μL
出荷条件湿氷
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
The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies.
Authors:Korbel JO, Tirosh-Wagner T, Urban AE, Chen XN, Kasowski M, Dai L, Grubert F, Erdman C, Gao MC, Lange K, Sobel EM, Barlow GM, Aylsworth AS, Carpenter NJ, Clark RD, Cohen MY, Doran E, Falik-Zaccai T, Lewin SO, Lott IT, McGillivray BC, Moeschler JB, Pettenati MJ, Pueschel SM, Rao KW, Shaffer LG, Shohat M, Van Riper AJ, Warburton D, Weissman S, Gerstein MB, Snyder M, Korenberg JR,
Journal:Proc Natl Acad Sci U S A
PubMed ID:19597142
'Down syndrome (DS), or trisomy 21, is a common disorder associated with several complex clinical phenotypes. Although several hypotheses have been put forward, it is unclear as to whether particular gene loci on chromosome 21 (HSA21) are sufficient to cause DS and its associated features. Here we present a high-resolution ... More
A single-molecule barcoding system using nanoslits for DNA analysis.
Authors:Jo K, Dhingra DM, Odijk T, de Pablo JJ, Graham MD, Runnheim R, Forrest D, Schwartz DC
Journal:Proc Natl Acad Sci U S A
PubMed ID:17296933
'Molecular confinement offers new routes for arraying large DNA molecules, enabling single-molecule schemes aimed at the acquisition of sequence information. Such schemes can rapidly advance to become platforms capable of genome analysis if elements of a nascent system can be integrated at an early stage of development. Integrated strategies are ... More
Lineage-specific DNA methylation in T cells correlates with histone methylation and enhancer activity.
Authors:Schmidl C, Klug M, Boeld TJ, Andreesen R, Hoffmann P, Edinger M, Rehli M,
Journal:Genome Res
PubMed ID:19494038
DNA methylation participates in establishing and maintaining chromatin structures and regulates gene transcription during mammalian development and cellular differentiation. With few exceptions, research thus far has focused on gene promoters, and little is known about the extent, functional relevance, and regulation of cell type-specific DNA methylation at promoter-distal sites. Here, ... More
A single-molecule barcoding system using nanoslits for DNA analysis : nanocoding.
Authors:Jo K, Schramm TM, Schwartz DC,
Journal:Methods Mol Biol
PubMed ID:19488691
Single DNA molecule approaches are playing an increasingly central role in the analytical genomic sciences because single molecule techniques intrinsically provide individualized measurements of selected molecules, free from the constraints of bulk techniques, which blindly average noise and mask the presence of minor analyte components. Accordingly, a principal challenge that ... More
Measuring, in solution, multiple-fluorophore labeling by combining fluorescence correlation spectroscopy and photobleaching.
Authors:Delon A, Wang I, Lambert E, Mache S, Mache R, Derouard J, Motto-Ros V, Galland R,
Journal:J Phys Chem B
PubMed ID:20143802
Determining the number of fluorescent entities that are coupled to a given molecule (DNA, protein, etc.) is a key point of numerous biological studies, especially those based on a single molecule approach. Reliable methods are important, in this context, not only to characterize the labeling process but also to quantify ... More