logo
AAT Bioquest

FITC-xtra maleimide

Product key features

  • Enhanced Photostability and Brighter Fluorescence: More resistant to photobleaching with a stronger signal than standard FITC.
  • Broad pH Stability: Maintains stable fluorescence across a pH range of 4 to 10.
  • High Conjugation Efficiency: Provides higher yields under mild reaction conditions than standard FITC
  • Spectral Compatibility and Optimal Excitation: Matches the spectral properties of FITC and is excitable by the 488 nm laser line.
  • Superior Signal-to-Background: Ensures improved accuracy and reliability in fluorescence assays.

Product description

FITC is widely used for creating green fluorescent bioconjugates; however, it has notable limitations, including significant photobleaching during microscopy and a fluorescence signal that is highly sensitive to pH variations. FITC-xtra addresses these challenges, providing a robust enhancement over traditional FITC. Bioconjugates prepared with FITC-xtra demonstrate significantly increased brightness and superior photostability compared to those labeled with standard FITC. Importantly, the fluorescence of FITC-xtra remains stable across a pH range of 4 to 10, addressing the limitation of FITC, which only reaches maximum fluorescence at pH levels above 9. Alongside these enhancements, FITC-xtra retains spectral properties nearly identical to FITC, ensuring compatibility. Moreover, FITC-xtra provides a higher conjugation yield under mild conditions compared to FITC. Like 5-FITC, FITC-xtra antibody conjugates are ideally excited by the 488 nm laser line, making them an excellent alternative to traditional FITC-labeled conjugates. When tested under identical conditions, FITC-xtra antibody conjugates consistently deliver higher signal-to-background ratios than their FITC counterparts.

The maleimide derivative of FITC-xtra is widely used for labeling biomolecules with free thiol (SH) groups, including antibodies, proteins, thiol-modified oligonucleotides, and low molecular weight ligands. Maleimides react readily with sulfhydryl groups, forming stable thio-ether bonds between the dye and the biomolecule, facilitating robust and reliable labeling for diverse experimental applications.

Spectrum

References

View all 50 references: Citation Explorer
Packaged europium/fluorescein-based hydrogen bond organic framework as ratiometric fluorescent probe for visual real-time monitoring of seafood freshness.
Authors: Li, Haiyan and Li, Min and Zhang, Shangqing and Chen, Mingli and Wang, Jianhua
Journal: Talanta (2024): 125809
Colorimetric aptasensor based on temporally controllable light-stimulated oxidase-mimicking fluorescein for the sensitive detection of exosomes in mild conditions.
Authors: Zheng, Li-E and Huang, Min and Liu, Yiyang and Bao, Qiufang and Huang, Yuxiu and Ye, Yuhong and Liu, Mengmeng and Sun, Pengming
Journal: Analytical methods : advancing methods and applications (2024): 3577-3586
Fluorescence Spectra of Prototropic Forms of Fluorescein and Some Derivatives and Their Potential Use for Calibration-Free pH Sensing.
Authors: Gauthier-Manuel, Bernard and Benmouhoub, Chafia and Wacogne, Bruno
Journal: Sensors (Basel, Switzerland) (2024)
A double-emission molecularly imprinted ratiometric fluorescent sensor based on carbon quantum dots and fluorescein isothiocyanate for visual detection of p-nitroaniline.
Authors: Li, Huiru and Tian, Yanbo and Tan, Liju and Wang, Na and Qiao, Yu and Wang, Jiangtao
Journal: Mikrochimica acta (2024): 377
Characterization and optimization of fluorescein isothiocyanate labeling of humanized h2E2 anti-cocaine mAb.
Authors: Kirley, Terence L and Norman, Andrew B
Journal: Biochemistry and biophysics reports (2023): 101520
Page updated on November 27, 2024

Ordering information

Price
Unit size
Catalog Number70180
Quantity
Add to cart

Additional ordering information

Telephone1-800-990-8053
Fax1-800-609-2943
Emailsales@aatbio.com
InternationalSee distributors
Bulk requestInquire
Custom sizeInquire
Technical SupportContact us
Purchase orderSend to sales@aatbio.com
ShippingStandard overnight for United States, inquire for international
Request quotation

Physical properties

Molecular weight

645.56

Solvent

DMSO

Spectral properties

Excitation (nm)

498

Emission (nm)

526

Storage, safety and handling

H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22

Storage

Freeze (< -15 °C); Minimize light exposure
UNSPSC12171501
Dye maleimides are among the most widely used reagents for covalently conjugating dyes to peptides, proteins, antibodies, and thiol-modified oligonucleotides or nucleic acids through their sulfhydryl (SH) groups. The maleimide functional group exhibits high specificity and reactivity towards thiol groups under physiological conditions, resulting in the formation of stable thioether bonds. This stability and efficiency make dye maleimides a valuable tool in various bioconjugation applications.
Dye maleimides are among the most widely used reagents for covalently conjugating dyes to peptides, proteins, antibodies, and thiol-modified oligonucleotides or nucleic acids through their sulfhydryl (SH) groups. The maleimide functional group exhibits high specificity and reactivity towards thiol groups under physiological conditions, resulting in the formation of stable thioether bonds. This stability and efficiency make dye maleimides a valuable tool in various bioconjugation applications.
Dye maleimides are among the most widely used reagents for covalently conjugating dyes to peptides, proteins, antibodies, and thiol-modified oligonucleotides or nucleic acids through their sulfhydryl (SH) groups. The maleimide functional group exhibits high specificity and reactivity towards thiol groups under physiological conditions, resulting in the formation of stable thioether bonds. This stability and efficiency make dye maleimides a valuable tool in various bioconjugation applications.