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Catalog Number:
23158
CAS Number:
160158-05-4
α-Fmoc-L-Lys((+)-Biotinyl-ε-aminocaproyl)-OH
Purity:
99%
Documents
$243.87 /250 mg
Taille
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Product Information

The compound a-Fmoc-L-Lys((+)-Biotinyl-e-aminocaproyl)-OH is a versatile building block in peptide synthesis, particularly valued in bioconjugation and drug delivery applications. This compound features a biotinyl group, which enhances its utility in affinity purification and targeted delivery systems, making it an excellent choice for researchers working in the fields of molecular biology and biochemistry. The Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy deprotection during peptide synthesis, facilitating the creation of complex peptide structures with high efficiency.

In practical applications, this compound is often utilized in the development of biotinylated peptides for use in assays, diagnostics, and therapeutic agents. Its unique structure not only provides stability but also improves the solubility of peptides in aqueous solutions, which is crucial for biological assays. Researchers can leverage the biotinylation for enhanced binding to streptavidin-coated surfaces, enabling precise targeting and detection in various experimental setups. Overall, a-Fmoc-L-Lys((+)-Biotinyl-e-aminocaproyl)-OH stands out for its multifunctionality and ease of use, making it an indispensable tool for advancing research in peptide chemistry and related fields.

CAS Number
160158-05-4
Purity
99%
Molecular Formula
C 37 H 49 N 5 OS
Molecular Weight
707.9
MDL Number
MFCD00672325
PubChem ID
20064901
Conditions
Conserver à 0-8°C
General Information
CAS Number
160158-05-4
Purity
99%
Molecular Formula
C 37 H 49 N 5 OS
Molecular Weight
707.9
MDL Number
MFCD00672325
PubChem ID
20064901
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

a-Fmoc-L-Lys((+)-Biotinyl-e-aminocaproyl)-OH is widely utilized in research focused on:

  • Bioconjugation: This compound serves as a versatile linker in bioconjugation processes, allowing researchers to attach biomolecules like proteins or antibodies to surfaces or other molecules, enhancing the specificity of assays and therapeutic agents.
  • Drug Development: In pharmaceutical research, it aids in the design of targeted drug delivery systems, improving the efficacy of treatments by ensuring that drugs reach their intended sites of action more effectively.
  • Protein Labeling: It is commonly used for labeling proteins with biotin, which can then be easily detected or purified using streptavidin-based techniques, streamlining the study of protein interactions and functions.
  • Diagnostics: The compound plays a crucial role in developing diagnostic tools, particularly in immunoassays, where biotinylated antibodies can enhance the sensitivity and specificity of disease detection.
  • Research in Molecular Biology: It is valuable in molecular biology applications, such as studying gene expression and protein interactions, providing researchers with a reliable tool for understanding complex biological processes.

Citations