Flamma® 648 Dichlorotriazine
Size of product (mg)
-
1 mg
-
5 mg
-
25 mg
Flamma® 648 Dichlorotriazine
Cat. No. List below
Description
Key features:
1. Excitation/Emission maxima: 648/667 nm
2. High extinction coefficient: ≥ 250,000 cm?¹M?¹
3. Low CF280: 0.02
4. Dichlorotriazine reactive group for specific hydroxyl labeling
5. Blue solid appearance
6. Molecular weight: 874.90 g/mol
7. Soluble in DMF and DMSO
Applications:
1. Polysaccharide labeling
2. Alcohol-containing biomolecule tagging
3. Advanced cellular labeling and detection
4. Glycoprotein research
5. Carbohydrate imaging studies
6. In vitro and in vivo imaging
Advantages:
1. Unique hydroxyl reactivity in aqueous solutions (pH >9)
2. Forms stable aryl ether linkages through irreversible chlorine displacement
3. Excellent optical properties when excited using 593 or 633 nm laser lines
4. High pH (>9) labeling allows for selective targeting of hydroxyl groups
5. Minimal reactivity with other nucleophiles under proper conditions
6. Bright and stable fluorescence signals for extended imaging sessions
7. Compatibility with common fluorescence instrumentation
- Fluorophore: Flamma® Fluors 648
- Reactive group: Dichlorotriazine
- Excitation/Emission Max.(nm): 648/667
- Spectrally similar dyes: Alexa647, DyLight650, Cy5
- Extinction coefficient: ≥ 250,000 cm-1M-1
- CF280: 0.02
- Appearance: Blue Solid
- Molecular Weight: 874.90 g/mol
- Solubility: DMF, DMSO
- Storage conditions: -20 ℃, protect from light
| Quick link (Cat.#) | Series | EXmax (nm) | EMmax (nm) | Spectrally similar dyes |
| PWR2112 | Flamma® 552 Dichlorotriazine | 550 | 564 | Alexa555, DyLight550, Cy3, ATTO550 |
| KWR2415 | Flamma® 581 Dichlorotriazine | 578 | 593 | Alexa594, DyLight594 |
| PWR2215 | Flamma® 648 Dichlorotriazine | 648 | 667 | Alexa647, DyLight650, Cy5 |
| PWR2515 | Flamma® 675 Dichlorotriazine | 675 | 691 | Alexa680, DyLight680, Cy5.5, IRDye680LT, CF680 |
| PWR2301 | Flamma® 749 Dichlorotriazine | 749 | 774 | Alexa750, DyLight755, Cy7.5, IRDye750 |
| PWR2603 | Flamma® 774 Dichlorotriazine | 774 | 800 | DyLight800, Cy7.5, IRDye800, CF770 |
Background
Flamma® Fluors
BioActs offers a broad range of Flamma® Fluors dyes equipped with variety of reactive and functional groups, which can cover the full spectral range from UV to NIR with their excellent fluorescence performance. Characteristic features of these superior dyes are strong absorption, high fluorescence quantum yield and high photostability. Flamma® dyes maintain good fluorescence activity and stability after conjugation to biomolecules and allow the detection of low-abundance biological structures with great sensitivity. The dyes are compatible with optical conditions of most of fluorescent equipment and are ideal for any applications in biological studies.
- Covering the full spectral range from UV to NIR
- Equipped with a variety of reactive groups: NHS and Sulfo-NHS ester, Vinylsulfone, Maleimide, Click chemistry, isothiocyanate, hydrazide and hydrophobic substances.
- High quantum yields and photostability
- High purity and compatible with most of biomolecules
- Versatile Excitation: Can be efficiently excited using 593 or 633 nm laser lines, compatible with common confocal microscopy setups.
- Excellent Optical Properties: Delivers bright, clear signals for high-quality imaging results.
- Specific Labeling: Ideal for targeted labeling of polysaccharides and alcohol-containing biomolecules.
- Stability: Forms stable aryl ether linkages for reliable, long-term imaging experiments.
Flamma® Fluors Dichlorotrazine
Flamma® Fluors dichlorotriazine is for labeling hydroxyl groups. Hydroxyls irreversibly displace one of chlorine at triazine ring via SNAr reaction pathway to yield an aryl ether linkage. Dichlorotriazines are among the few reactive groups that are reported to react directly with polysaccharides and other alcohols in aqueous solution, provided that the pH is >9 and other nucleophiles are not present.
Figure 1. Absorption (upper) and emission (bottom) spectra overlap of Flamma® Fluors
Figure 2. Immunofluorescence imaging and in situ hybridization imaging
Figure 3. Fluorescence images of Flamma® 749 (upper) and Flamma® 774 (bottom) carboxylic acid injected mouse model
Citation & Reference
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