Sulfosuccinimidyl 6-(biotinamido)hexanoate
95%
- Product Code: 64999
CAS:
127062-22-0
| Molecular Weight: | 556.59 g./mol | Molecular Formula: | C₂₀H₂₉N₄NaO₉S₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00078534 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C |
Product Description:
This chemical is widely used in bioconjugation processes, particularly for labeling proteins, peptides, and other biomolecules with biotin. Its primary application lies in facilitating the attachment of biotin to target molecules, enabling their detection or purification through biotin-streptavidin interactions. This is especially useful in techniques like ELISA, Western blotting, and immunohistochemistry, where biotinylated molecules are detected using streptavidin-linked enzymes or fluorescent tags. Additionally, it is employed in affinity chromatography to isolate specific biomolecules by leveraging the strong binding affinity between biotin and streptavidin. The compound’s water-soluble nature and efficient reactivity make it a valuable tool in molecular biology and biochemical research.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Off-White Powder |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | $742.47 |
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Sulfosuccinimidyl 6-(biotinamido)hexanoate
This chemical is widely used in bioconjugation processes, particularly for labeling proteins, peptides, and other biomolecules with biotin. Its primary application lies in facilitating the attachment of biotin to target molecules, enabling their detection or purification through biotin-streptavidin interactions. This is especially useful in techniques like ELISA, Western blotting, and immunohistochemistry, where biotinylated molecules are detected using streptavidin-linked enzymes or fluorescent tags. Additionally, it is employed in affinity chromatography to isolate specific biomolecules by leveraging the strong binding affinity between biotin and streptavidin. The compound’s water-soluble nature and efficient reactivity make it a valuable tool in molecular biology and biochemical research.
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