Date published: 2025-10-16

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Other Crosslinkers

Santa Cruz Biotechnology now offers a broad range of Crosslinkers for use in various applications. Crosslinkers are pivotal in scientific research as they enable the covalent bonding of molecules to study protein interactions, molecular structures, and biochemical pathways. These reagents facilitate the linking of two or more molecules, such as proteins or nucleic acids, which helps in stabilizing complex structures and understanding the spatial arrangement of biological macromolecules. The Other Crosslinkers category encompasses a diverse array of chemical entities designed to create specific and stable covalent bonds between target molecules under various experimental conditions. These compounds are essential in studying protein-protein interactions, mapping binding sites, and elucidating the architecture of macromolecular complexes. By employing these crosslinkers, researchers can capture transient interactions and stabilize delicate structures for analysis using techniques such as mass spectrometry, X-ray crystallography, and nuclear magnetic resonance (NMR) spectroscopy. Furthermore, crosslinkers are instrumental in the development of new materials, as they are used to modify surface properties, create hydrogels, and improve the mechanical strength of polymers. The versatility and specificity of Other Crosslinkers make them invaluable tools for advancing research in structural biology, biochemistry, and materials science. View detailed information on our available Other Crosslinkers by clicking on the product name.

Items 211 to 214 of 214 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

N-[2-[2-[2-[(N-Biotinyl-caproylamino)-ethoxy)ethoxyl]-4-[2-(trifluoromethyl)-3H-diazirin-3-yl]benzoyl]-1,3-bis(mannopyranosyl-4-yloxy)-2-propylamine

207971-25-3sc-224114
250 µg
$440.00
(0)

N-[2-[2-[2-[(N-Biotinyl-caproylamino)-ethoxy)ethoxyl]-4-[2-(trifluoromethyl)-3H-diazirin-3-yl]benzoyl]-1,3-bis(mannopyranosyl-4-yloxy)-2-propylamine exhibits remarkable crosslinking capabilities through its multifunctional structure. The presence of mannopyranosyl moieties enhances its affinity for specific biomolecules, enabling targeted interactions. Its trifluoromethyl diazirin group allows for photochemical activation, facilitating precise spatial control in crosslinking processes, while the ethoxy chains contribute to solubility and compatibility in diverse environments.

1,4-Butanediol diacrylate

1070-70-8sc-223020
sc-223020A
sc-223020B
sc-223020C
sc-223020D
25 ml
100 ml
1 L
20 L
60 L
$36.00
$56.00
$281.00
$1836.00
$4721.00
1
(1)

1,4-Butanediol diacrylate serves as a versatile crosslinker, characterized by its ability to form robust networks through radical polymerization. Its dual acrylate functionality promotes rapid reaction kinetics, enabling efficient crosslinking under UV light or thermal conditions. The compound's flexible aliphatic chain enhances the elasticity of the resulting polymers, while its low viscosity facilitates even distribution in formulations, ensuring uniform curing and improved mechanical properties.

1-Biotinylamino-3,6,9-trioxaundecane-11-yl-methanethiosulfonate

sc-213313
10 mg
$360.00
(0)

1-Biotinylamino-3,6,9-trioxaundecane-11-yl-methanethiosulfonate is a specialized crosslinker known for its unique ability to form stable thioether bonds, facilitating the creation of intricate molecular networks. Its distinctive trioxaundecane backbone provides a balance of hydrophilicity and hydrophobicity, influencing solubility and interaction with biomolecules. The biotinyl group enhances specificity in binding, allowing for targeted crosslinking in complex systems, while its reactive methanethiosulfonate moiety promotes efficient conjugation under mild conditions.

3-[2-N-(Biotinyl)aminoethyldithio]propanoic Acid

104582-29-8sc-206612A
sc-206612B
sc-206612
10 mg
50 mg
100 mg
$148.00
$235.00
$367.00
(0)

3-[2-N-(Biotinyl)aminoethyldithio]propanoic Acid is a versatile crosslinker characterized by its ability to form robust disulfide bonds, enabling the construction of complex polymeric architectures. The biotinyl moiety enhances affinity for streptavidin, facilitating selective interactions in diverse environments. Its dithioether functionality allows for efficient conjugation reactions, while the propanoic acid component contributes to solubility and reactivity, making it suitable for various biochemical applications.