logo
AAT Bioquest

ATTO 488 azide

Product Image
Product Image
Gallery Image 1
Ordering information
Price
Catalog Number
Unit Size
Quantity
Add to cart
Additional ordering information
Telephone1-800-990-8053
Fax1-800-609-2943
Emailsales@aatbio.com
InternationalSee distributors
Bulk requestInquire
Custom sizeInquire
ShippingStandard overnight for United States, inquire for international
Request quotation
Physical properties
Molecular weight657.67
SolventDMSO
Spectral properties
Correction Factor (260 nm)0.25
Correction Factor (280 nm)0.10
Extinction coefficient (cm -1 M -1)90000
Excitation (nm)499
Emission (nm)520
Quantum yield0.80
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
UNSPSC12171501

OverviewpdfSDSpdfProtocol


Molecular weight
657.67
Correction Factor (260 nm)
0.25
Correction Factor (280 nm)
0.10
Extinction coefficient (cm -1 M -1)
90000
Excitation (nm)
499
Emission (nm)
520
Quantum yield
0.80
ATTO 488 is a rhodamine-based fluorescent probe characterized by its excellent aqueous solubility and excellent spectral charactistics. It exhibits strong absorption, high fluorescence quantum yield, and outstanding photostability, making it particularly suitable for fluorescence imaging applications. ATTO 488 is highly effective for single-molecule detection and advanced high-resolution microscopy techniques such as PALM, dSTORM, and STED. Moreover, it is applicable in flow cytometry (FACS), fluorescence in-situ hybridization (FISH), and various other biological assays. The azide derivative of ATTO 488 can undergo a copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) with terminal alkynes to form 1,2,3-triazoles. It can also participate in Staudinger ligation with phosphine-containing molecules. Additionally, the azide group is reactive towards cyclooctynes and BCN moieties via strain-promoted azide-alkyne cycloaddition (SPAAC), facilitating copper-free bioorthogonal labeling reactions. These versatile reactivity profiles enhance the utility of ATTO 488 in various biochemical and molecular biology applications.

Calculators


Common stock solution preparation

Table 1. Volume of DMSO needed to reconstitute specific mass of ATTO 488 azide 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 mM152.052 µL760.26 µL1.521 mL7.603 mL15.205 mL
5 mM30.41 µL152.052 µL304.104 µL1.521 mL3.041 mL
10 mM15.205 µL76.026 µL152.052 µL760.26 µL1.521 mL

Molarity calculator

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

Mass (Calculate)Molecular weightVolume (Calculate)Concentration (Calculate)Moles
/=x=

Spectrum


Open in Advanced Spectrum Viewer
spectrum

Spectral properties

Correction Factor (260 nm)0.25
Correction Factor (280 nm)0.10
Extinction coefficient (cm -1 M -1)90000
Excitation (nm)499
Emission (nm)520
Quantum yield0.80

Product Family


NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)Quantum yieldCorrection Factor (260 nm)Correction Factor (280 nm)
iFluor® 488 azide4915167500010.910.210.11
ATTO 488 DBCO499520900000.800.250.10

Images


References


View all 32 references: Citation Explorer
Time-resolved fluorescence anisotropy with Atto 488-labeled phytochrome Agp1 from Agrobacterium fabrum.
Authors: Elkurdi, Afaf and Guigas, Gernot and Hourani-Alsharafat, Latifa and Scheerer, Patrick and Nienhaus, Gerd Ulrich and Krauß, Norbert and Lamparter, Tilman
Journal: Photochemistry and photobiology (2024): 561-572
Analysis of photon trajectories from diffusing single molecules.
Authors: Gopich, Irina V and Kim, Jae-Yeol and Chung, Hoi Sung
Journal: The Journal of chemical physics (2023)
Curvature preference of cubic CsPbBr3 quantum dots embedded onto phospholipid bilayer membranes.
Authors: Chairil, Ricki and Malmstadt, Noah
Journal: Soft matter (2023): 3966-3974
Interactions of the Kv1.1 Channel with Peptide Pore Blockers: A Fluorescent Analysis on Mammalian Cells.
Authors: Orlov, Nikita A and Kryukova, Elena V and Efremenko, Anastasia V and Yakimov, Sergey A and Toporova, Victoria A and Kirpichnikov, Mikhail P and Nekrasova, Oksana V and Feofanov, Alexey V
Journal: Membranes (2023)
Spatial distribution of single guest molecules along thickness of thin films of poly(2-hydroxyethyl acrylate).
Authors: Ito, Syoji and Hiratsuka, Kengo and Takei, Satoshi and Nishi, Hiroyasu and Kitagawa, Daichi and Kobatake, Seiya and Miyasaka, Hiroshi
Journal: Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society (2022): 175-184
Atto488-Agitoxin 2-A Fluorescent Ligand with Increased Selectivity for Kv1.3 Channel Binding Site.
Authors: Denisova, Kristina R and Orlov, Nikita A and Yakimov, Sergey A and Kirpichnikov, Mikhail P and Feofanov, Alexey V and Nekrasova, Oksana V
Journal: Bioengineering (Basel, Switzerland) (2022)
Lipophilic probe behavior in microemulsions evaluated by fluorescence correlation spectroscopy.
Authors: Yamamoto, Johtaro and Suzuki, Yoshio and Ogawa, Yoshikatsu and Kamata, Tomoyuki and Hashimoto, Hinako and Kunitake, Masashi and Kato, Dai
Journal: Analytical sciences : the international journal of the Japan Society for Analytical Chemistry (2022): 401-408
A Model of F-actin Organization in Granuloreticulopodia in Foraminifera: Morphogenetic and Evolutionary Implications from Novel Fluorescent and Polarised Light Observations.
Authors: Goleń, Jan and Tyszka, Jarosław and Godos, Karolina and Janse, Max
Journal: Protist (2022): 125886
Evaluation of [Cys(ATTO 488)8]Dermorphin-NH2 as a novel tool for the study of μ-opioid peptide receptors.
Authors: Giakomidi, Despina and Bird, Mark F and McDonald, John and Marzola, Erika and Guerrini, Remo and Chanoch, Serena and Sabu, Nidhuna and Horley, Barbara and Calo, Girolamo and Lambert, David G
Journal: PloS one (2021): e0250011
Multimodal fluorescently labeled polymer-coated GdF3 nanoparticles inhibit degranulation in mast cells.
Authors: Shapoval, Oleksandr and Sulimenko, Vadym and Klebanovych, Anastasiya and Rabyk, Mariia and Shapoval, Pavlo and Kaman, Ondřej and Rydvalová, Eliška and Filipová, Marcela and Dráberová, Eduarda and Dráber, Pavel and Horák, Daniel
Journal: Nanoscale (2021): 19023-19037