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XFD568 amine

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Physical properties
Molecular weight850.83
SolventDMSO
Spectral properties
Correction Factor (260 nm)0.45
Correction Factor (280 nm)0.46
Extinction coefficient (cm -1 M -1)88000
Excitation (nm)579
Emission (nm)603
Quantum yield0.691
Storage, safety and handling
H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22
StorageFreeze (< -15 °C); Minimize light exposure
Related products
XFD488 azide *Same Structure to Alexa Fluor™ 488 azide*
XFD488 alkyne *Same Structure to Alexa Fluor™ 488 alkyne*
XFD488 NHS Ester *Same Structure to Alexa Fluor™ 488 NHS Ester*
XFD488 C5 Maleimide *Same Structure to Alexa Fluor™ 488 C5 Maleimide*
XFD350 NHS Ester *Same Structure to Alexa Fluor™ 350 NHS Ester*
XFD532 NHS Ester *Same Structure to Alexa Fluor™ 532 NHS Ester*
XFD594 NHS Ester *Same Structure to Alexa Fluor™ 594 NHS Ester*
XFD350 C5 Maleimide *Same Structure to Alexa Fluor™ 350 C5 Maleimide*
XFD532 C5 Maleimide *Same Structure to Alexa Fluor™ 532 C5 Maleimide*
XFD594 C5 Maleimide *Same Structure to Alexa Fluor™ 594 C5 Maleimide*
XFD488 Hydroxylamine *Same Structure to Alexa Fluor™ 488 Hydroxylamine*
XFD350 goat anti-mouse IgG (H+L) *Cross Adsorbed, XFD350 Same Structure to Alexa Fluor™ 350*
XFD488 goat anti-mouse IgG (H+L) *Cross Adsorbed, XFD488 Same Structure to Alexa Fluor™ 488*
XFD594 goat anti-mouse IgG (H+L) *Cross Adsorbed, XFD594 Same Structure to Alexa Fluor™ 594*
XFD350 goat anti-rabbit IgG (H+L) *Cross Adsorbed, XFD350 Same Structure to Alexa Fluor™ 350*
XFD488 goat anti-rabbit IgG (H+L) *Cross Adsorbed, XFD488 Same Structure to Alexa Fluor™ 488*
XFD594 goat anti-rabbit IgG (H+L) *Cross Adsorbed, XFD594 Same Structure to Alexa Fluor™ 594*
XFD350-streptavidin conjugate *XFD350 Same Structure to Alexa Fluor™ 350*
XFD488-streptavidin conjugate *XFD488 Same Structure to Alexa Fluor™ 488*
XFD594-streptavidin conjugate *XFD594 Same Structure to Alexa Fluor™ 594*
XFD350 Phalloidin *XFD350 Same Structure to Alexa Fluor™ 350*
XFD488 Phalloidin *XFD488 Same Structure to Alexa Fluor™ 488*
XFD594 Phalloidin *XFD594 Same Structure to Alexa Fluor™ 594*
XFD532 acid *Same Structure to Alexa Fluor™ 532 acid*
XFD488 acid *Same Structure to Alexa Fluor™ 488 acid*
XFD488 tyramide reagent *Same Structure to Alexa Fluor™ 488 tyramide*
XFD546 tyramide reagent *Same Structure to Alexa Fluor™ 546 tyramide*
XFD594 tyramide reagent *Same Structure to Alexa Fluor™ 594 tyramide*
XFD488 NHS Ester-UltraPure Grade *XFD488 Same Structure to Alexa Fluor™ 488*
XFD555 NHS Ester *Same Structure to Alexa Fluor™ 555 NHS Ester*
XFD647 NHS Ester *Same Structure to Alexa Fluor™ 647 NHS Ester*
XFD680 NHS Ester *Same Structure to Alexa Fluor™ 680 NHS Ester*
XFD700 NHS Ester *Same Structure to Alexa Fluor™ 700 NHS Ester*
XFD750 NHS Ester *Same Structure to Alexa Fluor™ 750 NHS Ester*
XFD647 C2 Maleimide *Same Structure to Alexa Fluor™ 647 C2 Maleimide*
XFD546 NHS Ester *Same Structure to Alexa Fluor™ 546 NHS Ester*
XFD568 NHS Ester *Same Structure to Alexa Fluor™ 568 NHS Ester*
XFD350 tyramide reagent *Same Structure to Alexa Fluor™ 350 tyramide*
XFD568 tyramide reagent *Same Structure to Alexa Fluor™ 568 tyramide*
XFD350 acid *Same Structure to Alexa Fluor™ 350 acid*
XFD546 acid *Same Structure to Alexa Fluor™ 546 acid*
XFD488 tetrazine *Same Structure to Alexa Fluor™ 488 tetrazine*
XFD488 aldehyde *Same Structure to Alexa Fluor™ 488 aldehyde*
XFD™488-dUTP *1 mM in TE Buffer (pH 7.5)*
XFD514 acid
XFD514 NHS Ester *Same Structure to Alexa Fluor™ 514 NHS Ester*
XFD514 tyramide
XFD532 tyramide
XFD647 Azide
XFD647 Alkyne
XFD488 TCO
XFD555 acid
XFD647 acid
XFD750 acid
XFD700 acid
XFD647 Phalloidin *equivalent to Alexa Fluor® 647 phalloidin*
XFD405 NHS Ester [equivalent to Alexa Fluor™ 405 NHS Ester]
Show More (47)

OverviewpdfSDSpdfProtocol


Molecular weight
850.83
Correction Factor (260 nm)
0.45
Correction Factor (280 nm)
0.46
Extinction coefficient (cm -1 M -1)
88000
Excitation (nm)
579
Emission (nm)
603
Quantum yield
0.691
XFD568 amine is the same molecule to the Alexa Fluor® 568 amine (Alexa Fluor® is the trademark of ThermoFisher). It is a rhodamine dye with bright red-fluorescence optimal for labeling antibodies. XFD568 dye is water soluble and pH-insensitive from pH 4 to 10. The amine of XFD568 is a versatile carbonyl-reactive form for conjugating this fluorophore to peptides and other biological molecules.

Calculators


Common stock solution preparation

Table 1. Volume of DMSO needed to reconstitute specific mass of XFD568 amine to given concentration. Note that volume is only for preparing stock solution. Refer to sample experimental protocol for appropriate experimental/physiological buffers.

0.1 mg0.5 mg1 mg5 mg10 mg
1 mM117.532 µL587.661 µL1.175 mL5.877 mL11.753 mL
5 mM23.506 µL117.532 µL235.065 µL1.175 mL2.351 mL
10 mM11.753 µL58.766 µL117.532 µL587.661 µL1.175 mL

Molarity calculator

Enter any two values (mass, volume, concentration) to calculate the third.

Mass (Calculate)Molecular weightVolume (Calculate)Concentration (Calculate)Moles
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Spectrum


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spectrum

Spectral properties

Correction Factor (260 nm)0.45
Correction Factor (280 nm)0.46
Extinction coefficient (cm -1 M -1)88000
Excitation (nm)579
Emission (nm)603
Quantum yield0.691

Product Family


NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)Quantum yieldCorrection Factor (280 nm)
XFD488 amine *Same Structure to Alexa Fluor™ 488 amine*499520710000.9210.11
XFD594 amine *Same Structure to Alexa Fluor™ 594 amine*590618900000.6610.56
XFD568 acid *Same Structure to Alexa Fluor™ 568 acid*579603913000.6910.46
XFD532 amine534553810000.6110.09
XFD555 amine5535681550000.110.08
XFD647 amine6506712700000.3310.03
XFD750 amine7527762900000.1210.04
ICG amine789813230000-0.076

Images


References


View all 50 references: Citation Explorer
Enhancing interaction of actin and actin-binding domain 1 of dystrophin with modulators: Toward improved gene therapy for Duchenne muscular dystrophy.
Authors: Guhathakurta, Piyali and Carter, Anna L and Thompson, Andrew R and Kurila, Dillon and LaFrence, Jeffrey and Zhang, Li and Trask, Jake R and Vanderheyden, Bri and Muretta, Joseph M and Ervasti, James M and Thomas, David D
Journal: The Journal of biological chemistry (2022): 102675
Detection and quantification of the vacuolar H+ATPase using the Legionella effector protein SidK.
Authors: Maxson, Michelle E and Abbas, Yazan M and Wu, Jing Ze and Plumb, Jonathan D and Grinstein, Sergio and Rubinstein, John L
Journal: The Journal of cell biology (2022)
A naked antisense oligonucleotide with phosphorothioate linkages is taken up intracellularly more efficiently but functions less effectively.
Authors: Takahashi, Masayuki and Seki, Mineaki and Nashimoto, Masayuki
Journal: Biochemical and biophysical research communications (2021): 140-144
Dual-Labeled Graphene Quantum Dot-Based Förster Resonance Energy Transfer Nanoprobes for Single-Molecule Localization Microscopy.
Authors: Lu, Ju and Zong, Shenfei and Wang, Zhuyuan and Chen, Chen and Zhang, Yizhi and Wang, Hong and Cui, Yiping
Journal: ACS omega (2021): 8808-8815
Cardiac myosin-binding protein C interaction with actin is inhibited by compounds identified in a high-throughput fluorescence lifetime screen.
Authors: Bunch, Thomas A and Guhathakurta, Piyali and Lepak, Victoria C and Thompson, Andrew R and Kanassatega, Rhye-Samuel and Wilson, Anna and Thomas, David D and Colson, Brett A
Journal: The Journal of biological chemistry (2021): 100840
Switching behaviour of dSTORM dyes in glycerol-containing buffer.
Authors: Goossen-Schmidt, Nora C and Schnieder, Marco and Hüve, Jana and Klingauf, Jürgen
Journal: Scientific reports (2020): 13746
Effect of amisulpride, olanzapine, quetiapine, and aripiprazole single administration on c-Fos expression in vasopressinergic and oxytocinergic neurons of the rat hypothalamic supraoptic nucleus.
Authors: Kiss, Alexander and Osacka, Jana
Journal: Endocrine regulations (2020): 77-84
Hot-Band Anti-Stokes Fluorescence Properties of Alexa Fluor 568.
Authors: Gajdos, Tamás and Hopp, Béla and Erdélyi, Miklós
Journal: Journal of fluorescence (2020): 437-443
Suppression of Connexin 43 Leads to Strial Vascular Hyper-Permeability, Decrease in Endocochlear Potential, and Mild Hearing Loss.
Authors: Zhang, Jinhui and Wang, Xiaohan and Hou, Zhiqiang and Neng, Lingling and Cai, Jing and Zhang, Yunpei and Shi, Xiaorui
Journal: Frontiers in physiology (2020): 974
Phosphatidylserine Asymmetry Promotes the Membrane Insertion of a Transmembrane Helix.
Authors: Scott, Haden L and Heberle, Frederick A and Katsaras, John and Barrera, Francisco N
Journal: Biophysical journal (2019): 1495-1506