N-(17-Amino-3,6,9,12,15-pentaoxaheptadecyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide
97%
- Product Code: 109003
CAS:
113072-75-6
Molecular Weight: | 506.66 g./mol | Molecular Formula: | C₂₂H₄₂N₄O₇S |
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EC Number: | MDL Number: | MFCD22574819 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | -20°C, sealed, dry, away from light |
Product Description:
This chemical is primarily utilized in the field of biotechnology and molecular biology, where it serves as a crucial component in the modification and functionalization of biomolecules. Its structure, featuring a biotin moiety and a hydrophilic spacer, makes it highly effective for conjugation with proteins, peptides, or other biomolecules. This conjugation enhances the binding affinity to avidin or streptavidin, which is essential in applications such as immunoassays, histochemistry, and biosensors. Additionally, it is employed in the development of targeted drug delivery systems, where it aids in the precise attachment of therapeutic agents to specific cellular targets. Its water-soluble nature ensures compatibility with aqueous biological environments, facilitating its use in various diagnostic and therapeutic platforms.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿93,546.00 |
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N-(17-Amino-3,6,9,12,15-pentaoxaheptadecyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide
This chemical is primarily utilized in the field of biotechnology and molecular biology, where it serves as a crucial component in the modification and functionalization of biomolecules. Its structure, featuring a biotin moiety and a hydrophilic spacer, makes it highly effective for conjugation with proteins, peptides, or other biomolecules. This conjugation enhances the binding affinity to avidin or streptavidin, which is essential in applications such as immunoassays, histochemistry, and biosensors. Additionally, it is employed in the development of targeted drug delivery systems, where it aids in the precise attachment of therapeutic agents to specific cellular targets. Its water-soluble nature ensures compatibility with aqueous biological environments, facilitating its use in various diagnostic and therapeutic platforms.
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