Atto 488 amine

Name: Atto 488 amine
Brand: SIGMA

BioReagent, ≥90% (HPLC), suitable for fluorescence

Select a Size

All Photos(1)

About This Item

NACRES:

NA.32

UNSPSC Code:

12352116

Product Name

Atto 488 amine, BioReagent, ≥90% (HPLC), suitable for fluorescence

product line

BioReagent

assay

≥90% (HPLC)

form

solid

mol wt

M_w 858 g/mol

manufacturer/tradename

ATTO-TEC GmbH

λ

in methanol: water (1:1) (with 0.1% perchloric acid)

UV absorption

λ: 502-508 nm A_max

suitability

suitable for fluorescence

storage temp.

−20°C

Quality Level

100

General description

Atto 488 is a fluorescent label with excellent water solubility. Characteristic features of the label are strong absorption, high fluorescence quantum yield, high photostability, and very little triplet formation. Thus Atto 488 is highly suitable for single-molecule detection applications and high-resolution microscopy such as PALM, dSTORM, STED etc. Additionally the dye highly qualifies to be applied in flow cytometry (FACS), fluorescence in-situ hybridization (FISH) and many more. The fluorescence is excited most efficiently in the range 480 - 515 nm. For instance the 488 nm line of the Argon-Ion laser is very suitable for excitation.

find more information here

Legal Information

This product is for Research use only. In case of intended commercialization, please contact the IP-holder (ATTO-TEC GmbH, Germany) for licensing.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Analysis of fluorescent nanostructures in biological systems by means of spectral position determination microscopy (SPDM).

Muller, P., et al. et al.

Current Microscopy Contributions to Advances in Science and Technology, 1, 3-12 (2012)

Monitoring single membrane protein dynamics in a liposome manipulated in solution by the ABELtrap.

Rendler, T., et al.

arXiv, 1102-1102 (2011)

Subcellular location, phosphorylation and assembly into the motor complex of GAP45 during Plasmodium falciparum schizont development.

Mohd A Mohd Ridzuan et al.

PloS one, 7(3), e33845-e33845 (2012-04-06)

An actomyosin motor complex assembled below the parasite's plasma membrane drives erythrocyte invasion by Plasmodium falciparum merozoites. The complex is comprised of several proteins including myosin (MyoA), myosin tail domain interacting protein (MTIP) and glideosome associated proteins (GAP) 45 and

Kinetics of diffusion-mediated DNA hybridization in lipid monolayer films determined by single-molecule fluorescence spectroscopy.

Jonas K Hannestad et al.

ACS nano, 7(1), 308-315 (2012-12-12)

We use single-molecule fluorescence microscopy to monitor individual hybridization reactions between membrane-anchored DNA strands, occurring in nanofluidic lipid monolayer films deposited on Teflon AF substrates. The DNA molecules are labeled with different fluorescent dyes, which make it possible to simultaneously

Spotiton: a prototype for an integrated inkjet dispense and vitrification system for cryo-TEM.

Tilak Jain et al.

Journal of structural biology, 179(1), 68-75 (2012-05-10)

Over the last three decades, Cryo-TEM has developed into a powerful technique for high-resolution imaging of biological macromolecules in their native vitrified state. However, the method for vitrifying specimens onto EM grids is essentially unchanged - application of ∼3 μL

View All Related Papers