Labeling-detection

AnaTag™ HiLyte™ Fluor 488 Protein Labeling Kit - 1 kit

454.00
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  • Cat.Number : AS-72047
  • Availability :
    In stock
  • Shipping conditions : Ice delivery fees must be applied

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HiLyte™ Fluor 488, SE is an excellent amine-reactive fluorescent labeling dye for generating protein conjugates. The spectrum of HiLyte™ Fluor 488 is similar to fluorescein (FITC), resulting in an optimal match to filters designed for fluorescein. HiLyte™ Fluor 488 is more photostable than FITC, providing researchers with additional time for capturing image. Its fluorescence can be detected at the emission wavelength of 523±10 nm when excited at 499±10 nm. The HiLyte™ Fluor 488-protein conjugates are very stable and suitable for immunofluorescent staining, in situ hybridization, flow cytometry and other biological applications. The kit has all essential components for performing the conjugation reaction and for purifying the HiLyte™ Fluor 488-protein conjugate. The entire process takes only half an hour. The kit is able to perform three conjugation reactions with each reaction labeling up to 5 mg IgG.
Note: AnaTag kits are not intended for peptide labeling.

Specifications

Packaging
Kits components
  • Component A: HiLyte™ Fluor 488 SE Amino-reactive dye: 3 vials Component B: Reaction buffer for pH adjustment of the conjugation reaction: 0.5 mL Component C: Spin column to purify dye-protein conjugate: 3 pre-packed columns Component D: DMSO solvent for preparing dye stock solution: 1 mL Component E: 10x Elution buffer for eluting dye-protein conjugate: 30 mL
Properties
Absorbance (nm)
  • 499
Emission (nm)
  • 523
Storage & stability
Storage Conditions
  • Store component A at -20°C. Store all other components at 4°C. Protect component A from light and moisture.
Activity
Application
Detection Method
Research Area
Sub-category Research Area
Usage
  • Research use
Codes
Code Nacres
  • NA.32

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Citations

Live Cell Imaging Reveals Actin-Cytoskeleton-Induced Self-Association of the Actin-Bundling Protein WLIM1.

J Cell Sci . 2013 Nov 27 ; 127(Pt3) 583 | DOI : 10.1242/​jcs.134536

  • C. Hoffmann
  • et al