logo
AAT Bioquest

Tide Fluor™ 3 maleimide [TF3 maleimide] *Superior replacement for Cy3*

Related products
Tide Fluor™ 1 azide [TF1 azide]
Tide Fluor™ 1 alkyne [TF1 alkyne]
Tide Fluor™ 1 acid [TF1 acid] *Superior replacement for EDANS*
Tide Fluor™ 1 amine [TF1 amine] *Superior replacement for EDANS*
Tide Fluor™ 1 CPG [TF1 CPG] *500 Å* *Superior replacement for EDANS*
Tide Fluor™ 1 CPG [TF1 CPG] *1000 Å* *Superior replacement for EDANS*
Tide Fluor™ 1 succinimidyl ester [TF1 SE]*Superior replacement for EDANS*
Tide Fluor™ 2 acid [TF2 acid] *Superior replacement for fluorescein*
Tide Fluor™ 2 amine [TF2 amine] *Superior replacement for fluorescein*
Tide Fluor™ 2, succinimidyl ester [TF2 SE]*Superior replacement for fluorescein*
Tide Fluor™ 2 azide [TF2 azide]
Tide Fluor™ 2 alkyne [TF2 alkyne]
Tide Fluor™ 3 succinimidyl ester [TF3 SE]*Superior replacement for Cy3*
Tide Fluor™ 5WS azide [TF5WS azide]
Tide Fluor™ 5WS alkyne [TF5WS alkyne]
Tide Fluor™ 5WS acid [TF5WS acid] *Superior replacement for Cy5*
Tide Fluor™ 5WS amine [TF5WS amine] *Superior replacement for Cy5*
Tide Fluor™ 5WS succinimidyl ester [TF5WS SE]*Superior replacement for Cy5*
Tide Fluor™ 4 acid [TF4 acid] *Superior replacement for ROX and Texas Red*
Tide Fluor™ 4 amine [TF4 amine] *Superior replacement for ROX and Texas Red*
Tide Fluor™ 4, succinimidyl ester [TF4 SE]*Superior replacement for ROX and Texas Red*
Tide Fluor™ 6WS acid [TF6WS acid] *Superior replacement for Cy5.5*
Tide Fluor™ 6WS amine [TF6WS amine] *Superior replacement for Cy5.5*
Tide Fluor™ 6WS succinimidyl ester [TF6WS SE]*Superior replacement for Cy5.5*
Tide Fluor™ 4 azide [TF4 azide]
Tide Fluor™ 4 alkyne [TF4 alkyne]
Tide Fluor™ 6WS azide [TF6WS azide]
Tide Fluor™ 6WS alkyne [TF6WS alkyne]
Tide Fluor™ 7WS azide [TF7WS azide]
Tide Fluor™ 7WS alkyne [TF7WS alkyne]
Tide Fluor™ 8WS azide [TF8WS azide] *Near Infrared Emission*
Tide Fluor™ 8WS alkyne [TF8WS alkyne] *Near Infrared Emission*
Tide Fluor™ 7WS acid [TF7WS acid] *Superior replacement for Cy7*
Tide Fluor™ 7WS amine [TF7WS amine] *Superior replacement for Cy7*
Tide Fluor™ 7WS, succinimidyl ester [TF7WS SE]*Superior replacement for Cy7*
Tide Fluor™ 8WS acid [TF8WS acid] *Near Infrared Emission*
Tide Fluor™ 8WS amine [TF8WS amine] *Near Infrared Emission*
Tide Fluor™ 8WS, succinimidyl ester [TF8WS SE]*Near Infrared Emission*
Tide Fluor™ 3WS acid [TF3WS acid] *Superior replacement for Cy3*
Tide Fluor™ 3WS succinimidyl ester [TF3WS SE] *Superior replacement for Cy3*
Tide Fluor™ 3WS amine [TF3WS amine] *Superior replacement for Cy3*
Tide Fluor™ 2WS acid [TF2WS acid] *Superior replacement for FITC*
Tide Fluor™ 2WS succinimidyl ester [TF2WS SE] *Superior replacement for FITC*
Tide Fluor™ 2WS Amine [TF2WS amine] *Superior replacement for FITC*
Show More (34)
Tide Fluor™ 3 (TF3) family has the spectral properties essentially identical to those of Cy3. Compared to Cy3 probes TF3 family has much stronger fluorescence and higher photostability. Additionally their fluorescence is pH-independent from pH 3 to 11. These characteristics make this new dye family a superior alternative to Cy3. TF3-labeled peptides and nucleotides exhibit much stronger fluorescence and higher photostability than the ones labeled with Cy3. In pairing with our Tide Quencher™ 3 (TQ3), a variety of FRET peptides and nucleotides can be developed for detecting proteases and molecular beacons with enhanced sensitivity and stability. This TF3 product is used for post-labeling of thiol-modified oligonucleotides and peptides that contain cysteines.
Fluorescent dye maleimides are the most popular tool for conjugating dyes to a peptide, protein, antibody, thiol-modified oligonucleotide or nucleic acid through their SH group. Maleimides react readily with the thiol group of proteins, thiol-modified oligonucleotides, and other thiol-containing molecules under neutral conditions. The resulting dye conjugates are quite stable.
Fluorescent dye maleimides are the most popular tool for conjugating dyes to a peptide, protein, antibody, thiol-modified oligonucleotide or nucleic acid through their SH group. Maleimides react readily with the thiol group of proteins, thiol-modified oligonucleotides, and other thiol-containing molecules under neutral conditions. The resulting dye conjugates are quite stable.
Fluorescent dye maleimides are the most popular tool for conjugating dyes to a peptide, protein, antibody, thiol-modified oligonucleotide or nucleic acid through their SH group. Maleimides react readily with the thiol group of proteins, thiol-modified oligonucleotides, and other thiol-containing molecules under neutral conditions. The resulting dye conjugates are quite stable.
Ordering information
Price
Unit size
Catalog Number2270
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 weight651.71
SolventDMSO
Spectral properties
Correction Factor (280 nm)0.179
Extinction coefficient (cm -1 M -1)750001
Excitation (nm)554
Emission (nm)578
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
Calculators

Common stock solution preparation

Table 1. Volume of DMSO needed to reconstitute specific mass of Tide Fluor™ 3 maleimide [TF3 maleimide] *Superior replacement for Cy3* 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 mM153.442 µL767.212 µL1.534 mL7.672 mL15.344 mL
5 mM30.688 µL153.442 µL306.885 µL1.534 mL3.069 mL
10 mM15.344 µL76.721 µL153.442 µL767.212 µL1.534 mL

Molarity calculator

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

Mass (Calculate)Molecular weightVolume (Calculate)Concentration (Calculate)Moles
/=x=
Spectrum
Citations
View all 11 citations: Citation Explorer
To what extent do fluorophores bias the biological activity of peptides? A practical approach using membrane-active peptides as models
Authors: Cavaco, Marco and P{\'e}rez-Peinado, Clara and Valle, Javier and Silva, R{\'u}ben DM and Correia, Jo{\~a}o DG and Andreu, David and Castanho, Miguel ARB and Neves, Vera
Journal: Frontiers in bioengineering and biotechnology (2020): 552035
RAB33B recruits the ATG16L1 complex to the phagophore via a noncanonical RAB binding protein
Authors: Pantoom, Supansa and Konstantinidis, Georgios and Voss, Stephanie and Han, Hongmei and Hofnagel, Oliver and Li, Zhiyu and Wu, Yao-Wen
Journal: Autophagy (2020): 1--15
A mechanistic model to predict effects of cathepsin B and cystatin C on &beta;-amyloid aggregation and degradation
Authors: Perlenfein, Tyler J and Murphy, Regina M
Journal: Journal of Biological Chemistry (2017): jbc--M117
Using a Specific RNA--Protein Interaction To Quench the Fluorescent RNA Spinach
Authors: Roszyk, Laura and Kollenda, Sebastian and Hennig, Sven
Journal: ACS chemical biology (2017): 2958--2964
Spatiotemporal imaging of small GTPases activity in live cells
Authors: Voss, Stephanie and Kr{\"u}ger, Dennis M and Koch, Oliver and Wu, Yao-Wen
Journal: Proceedings of the National Academy of Sciences (2016): 14348--14353
References
View all 25 references: Citation Explorer
Photodynamic molecular beacon triggered by fibroblast activation protein on cancer-associated fibroblasts for diagnosis and treatment of epithelial cancers
Authors: Lo PC, Chen J, Stefflova K, Warren MS, Navab R, B and archi B, Mullins S, Tsao M, Cheng JD, Zheng G.
Journal: J Med Chem (2009): 358
Time-resolved FRET method for typing polymorphic alleles of the human leukocyte antigen system by using a single DNA probe
Authors: Andreoni A, Bondani M, Nardo L.
Journal: Photochem Photobiol Sci (2009): 1202
Tumor-specific detection of an optically targeted antibody combined with a quencher-conjugated neutravidin "quencher-chaser": a dual "quench and chase" strategy to improve target to nontarget ratios for molecular imaging of cancer
Authors: Ogawa M, Kosaka N, Choyke PL, Kobayashi H.
Journal: Bioconjug Chem (2009): 147
The detection of platelet derived growth factor using decoupling of quencher-oligonucleotide from aptamer/quantum dot bioconjugates
Authors: Kim GI, Kim KW, Oh MK, Sung YM.
Journal: Nanotechnology (2009): 175503
Development of a cell-based hepatitis C virus infection fluorescent resonance energy transfer assay for high-throughput antiviral compound screening
Authors: Yu X, Sainz B, Jr., Uprichard SL.
Journal: Antimicrob Agents Chemother (2009): 4311