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Catalog Number:
32936
CAS Number:
1926163-67-8
Fluorescéine-6-carbonyl-Leu-Glu(OMe)-His-DL-Asp(OMe)-fluorométhylcétone
Synonym(s):
["["Bis(1, 1-diméthyléthyl)azodicarboxylate, [DBAD »]
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Product Information

Fluorescein-6-carbonyl-Leu-Glu(OMe)-His-DL-Asp(OMe)-fluoromethylketone is a specialized fluorescent probe that combines the properties of fluorescein with a peptide sequence, making it an invaluable tool in biochemical research and diagnostics. This compound is particularly useful in studying protein interactions, cellular processes, and enzyme activities due to its unique fluorescent properties. Researchers can utilize this probe for real-time imaging in live cells, allowing for the observation of dynamic biological processes with high sensitivity and specificity.

The incorporation of amino acids such as Leucine, Glutamic acid, Histidine, and Aspartic acid enhances its binding capabilities and selectivity towards target biomolecules, making it suitable for applications in drug discovery and development. Its fluoromethylketone functionality allows for covalent labeling of proteins, facilitating the study of protein dynamics and interactions in complex biological systems. With its unique combination of fluorescence and peptide characteristics, this compound stands out as a versatile tool for researchers aiming to advance their understanding of cellular mechanisms and therapeutic targets.

Synonyms
["["Bis(1, 1-diméthyléthyl)azodicarboxylate, [DBAD »]
CAS Number
1926163-67-8
Molecular Formula
C 45 H 47 FN 6 O 14
Molecular Weight
914.9
MDL Number
MFCD09037416
Conditions
Conserver à ≤ -10 °C
General Information
Synonyms
["["Bis(1, 1-diméthyléthyl)azodicarboxylate, [DBAD »]
CAS Number
1926163-67-8
Molecular Formula
C 45 H 47 FN 6 O 14
Molecular Weight
914.9
MDL Number
MFCD09037416
Conditions
Conserver à ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fluorescein-6-carbonyl-Leu-Glu(OMe)-His-DL-Asp(OMe)-fluoromethylketone is widely utilized in research focused on:

  • Bioconjugation: This compound serves as a versatile tool for labeling biomolecules, enabling researchers to track and visualize proteins and nucleic acids in various biological systems.
  • Fluorescent Imaging: Its fluorescent properties make it ideal for applications in microscopy, allowing scientists to observe cellular processes in real-time with high sensitivity and resolution.
  • Drug Development: The compound can be used in the design of targeted therapeutics, helping to deliver drugs specifically to cancer cells or other diseased tissues, enhancing treatment efficacy.
  • Peptide Synthesis: This chemical can be incorporated into peptide sequences to study interactions and functions of specific amino acids, aiding in the development of new biomaterials.
  • Diagnostics: It has potential applications in developing diagnostic tools, such as assays for detecting specific biomarkers in diseases, thus facilitating early diagnosis and treatment.

Citations