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SEEBRIGHT® Red 580 dUTP (lyophilized)

 
ENZ-42844L-0050 50 nmol 633.00 USD
Do you need bulk/larger quantities?
 
For ready-to-use, aqueous format, see ENZ-42844.
Red 580 [5-ROX] dUTP can replace TTP in reactions in which it serves as a substrate for E. coli DNA polymerase (holoenzyme and Klenow fragment), T4 and Taq DNA polymerases, reverse transcriptase (from AMV and M-MuLV) and terminal transferase. Fluorescently labeled probes can be prepared with this fluorescent nucleotide by a variety of methods including nick translation, random prime labeling, cDNA labeling and 3’-end labeling. Probes generated by these methods are suitable for use for the identification of specific sequences by in situ hybridization procedures on fixed cells and tissues by direct fluorescence detection. Red 580 dUTP can also be used for multicolor fluorescence labeling.

This labeled dUTP can be used with the Nick Translation DNA Labeling System 2.0 (Prod. No. ENZ-GEN111).

Product Details

Alternative Name:5-ROX dUTP
 
Quantity:Sufficient for approximately 98 reactions, following the recommended protocol of Prod. No. ENZ-GEN111.
 
Formulation:Lyophilized.
 
Excitation maximum:580 nm
 
Emission maximum:603 nm
 
Extinction Coefficient:75,000 M-1 cm-1 (580 nm in TE [10 mM TRIS, pH 8.0, 1 mM EDTA])
 
Correction Factor (260 nm):0.44
 
Correction Factor (280 nm):0.40
 
Purity:≥93% (HPLC)
 
Appearance:Purple solid.
 
Applications:FISH
 
Shipping:Dry Ice
 
Long Term Storage:-20°C
 
Handling:Protect from light. Avoid freeze/thaw cycles.
 
Technical Info/Product Notes:Several of Enzo’s products and product applications are covered by US and foreign patents and patents pending.
 
Regulatory Status:RUO - Research Use Only
 
SEEBRIGHT™ Red 580 dUTP (lyophilized) image
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Product Literature References

Structural and spatial chromatin features at developmental gene loci in human pluripotent stem cells: H. Ikeda, et al.; Nat. Commun. 8, 1616 (2017), Application(s): Generation of FISH probes, Abstract; Full Text
Subtyping of renal cortical neoplasms in fine needle aspiration biopsies using a decision tree based on genomic alterations detected by fluorescence in situ hybridization: B. Gowrishankar, et al.; BJU Int. 114, 881 (2014), Abstract; Full Text

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