Alexa Fluor™ 647-aha-dCTP
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Invitrogen™

Alexa Fluor™ 647-aha-dCTP

The Alexa Fluor® 647 dyes, used to label nucleotides, are compatible with commonly used microarray scanners, and provide greater signalRead more
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Catalog NumberQuantity
A3277150 μL
Catalog number A32771
Price (CNY)
9,784.94
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Ends: 31-Dec-2025
11,765.00
Save 1,980.06 (17%)
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Quantity:
50 μL
Price (CNY)
9,784.94
飞享价
Ends: 31-Dec-2025
11,765.00
Save 1,980.06 (17%)
Each
Add to cart
The Alexa Fluor® 647 dyes, used to label nucleotides, are compatible with commonly used microarray scanners, and provide greater signal correlation (R2) valuesthan the spectrally similar Cy™3 and Cy™5 dye pair, improving the resolution of two-color microarray gene expression assays to 1.3-fold changes in expression. The exceptionally bright and photostable Alexa Fluor® dyes are also essentially insensitive tob pH and are highly water soluble.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
AssayMicroarray Gene Expression Assay
Concentration1 mM
Labeling MethodDirect Labeling
Label or DyeAlexa Fluor Dye
ModificationAHA (5-aminohexylacrylamido)
Product LineAlexa Fluor
Product TypeLabeled Nucleotide
Quantity50 μL
Shipping ConditionWet Ice
Unit SizeEach
Contents & Storage
Store in freezer (-5 to -30°C) and protect from light.

Citations & References (5)

Citations & References
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