Biotin-C4-amide-C5-NH2 - CAS 151294-96-1

Biotin-C4-amide-C5-NH2 - CAS 151294-96-1 Catalog number: BADC-01515

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Biotin-C4-amide-C5-NH2 is a highly regarded compound in the biomedical field and is of vital importance due to its multifaceted role in therapeutic intervention. It facilitates the development of drugs to combat a variety of diseases, including but not limited to cancer, diabetes, and neurological disorders.

Category
ADCs Linker
Product Name
Biotin-C4-amide-C5-NH2
CAS
151294-96-1
Catalog Number
BADC-01515
Molecular Formula
C14H26N4O2S
Molecular Weight
314.45
Biotin-C4-amide-C5-NH2

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BADC-01515 -- $--
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Description
Biotin-C4-amide-C5-NH2 is a highly regarded compound in the biomedical field and is of vital importance due to its multifaceted role in therapeutic intervention. It facilitates the development of drugs to combat a variety of diseases, including but not limited to cancer, diabetes, and neurological disorders.
Synonyms
Biotin-C4-amide-C5-NH2
IUPAC Name
N-(4-aminobutyl)-5-[(3aS,4S)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanamide
Canonical SMILES
C1C2C(C(S1)CCCCC(=O)NCCCCN)NC(=O)N2
InChI
InChI=1S/C14H26N4O2S/c15-7-3-4-8-16-12(19)6-2-1-5-11-13-10(9-21-11)17-14(20)18-13/h10-11,13H,1-9,15H2,(H,16,19)(H2,17,18,20)/t10?,11-,13-/m0/s1
InChIKey
RHLVNHVKSXNHES-KUNJKIHDSA-N

Biotin-C4-amide-C5-NH2, a versatile biotinylation reagent, boasts a wide array of applications in biochemical and biomedical research. Here are four key applications presented with a high degree of perplexity and burstiness:

Protein Purification: By employing Biotin-C4-amide-C5-NH2, scientists biotinylate proteins, facilitating their purification through streptavidin or avidin affinity columns. This innovative method ensures the isolation of target proteins with exceptional purity from complex mixtures, proving indispensable in both preparative and analytical contexts where pristine protein isolation is paramount.

Protein-Protein Interaction Studies: Through the biotinylation of proteins using Biotin-C4-amide-C5-NH2, researchers can delve into and quantify protein-protein interactions via streptavidin-based assays. Widely employed in co-immunoprecipitation and pull-down assays, this method sheds light on intracellular signaling complexes and protein binding affinities. It aids in uncovering novel interaction partners and unraveling intricate protein networks.

Imaging and Localization: Serving as a valuable tool for labeling biomolecules, Biotin-C4-amide-C5-NH2 enables high-resolution visualization of cellular and subcellular structures in techniques like immunofluorescence and electron microscopy. Detecting biotinylated molecules with fluorescence or gold-labeled streptavidin allows for exploring spatial distribution and dynamics of target molecules within cellular environments.

Enzyme-Linked Assays: In the realm of enzyme-linked assays, Biotin-C4-amide-C5-NH2 plays a pivotal role in biotinylating antibodies, antigens, or other assay components. Detecting biotinylated molecules using streptavidin-conjugated enzymes facilitates highly sensitive and specific detection methods such as ELISAs. This advancement enhances the signal-to-noise ratio, enabling precise quantification of low-abundance analytes across diverse samples.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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