Name: Medetomidine BSA conjugate
Brand: AAT Bioquest
SKU: 50655
Price: 989 USD
Availability: InStock

Medetomidine BSA conjugate

Medetomidine BSA conjugate is an immunogenic hapten-carrier complex linking medetomidine to bovine serum albumin, designed for generating specific antibodies for therapeutic drug monitoring and immunoassay development.

Preserved Epitope Integrity: Conjugation strategy maintains the structural and functional integrity of the medetomidine moiety
High-Purity Immunogen: Medetomidine is covalently linked to BSA via defined linker chemistry for consistent and stable conjugation
Optimized for Immunoassays: Suitable for use in ELISA, competitive binding assays, and lateral flow applications targeting medetomidine
Reliable Antibody Generation: Engineered for robust immune response and high-affinity antibody production

The chemical structure of Medetomidine BSA conjugate.

Datasheet

SDS

COA

Catalog	Size	Price	Quantity
50655	1 mg	Price

Overview

The Medetomidine-BSA conjugate is a synthetic immunogen designed for the generation of antibodies against medetomidine, a selective α2-adrenergic receptor agonist commonly used in veterinary anesthesia and research. Due to its low molecular weight and limited immunogenicity, medetomidine must be conjugated to a carrier protein to elicit a robust immune response. In this construct, medetomidine is covalently linked to bovine serum albumin (BSA) via a chemically defined linker, ensuring stable attachment while preserving the pharmacologically relevant epitope. This conjugate is suitable for applications in antibody production and the development of immunoassays such as ELISA, competitive binding assays, and lateral flow devices for the qualitative or quantitative detection of medetomidine or structurally related compounds. This reagent is intended for research use only and is not approved for diagnostic or therapeutic applications.

References

View all 50 references: Citation Explorer

Contribution of UGT Enzymes to Human Drug Metabolism Stereoselectivity: A Case Study of Medetomidine, RO5263397, Propranolol, and Testosterone.

Authors:

Milani, Nicolò and Qiu, NaHong and Fowler, Stephen

Journal:

Drug metabolism and disposition: the biological fate of chemicals (2023): 306-317

Ligand- and Structure-Based Analysis of Deep Learning-Generated Potential α2a Adrenoceptor Agonists.

Authors:

Schultz, Katherine J and Colby, Sean M and Lin, Vivian S and Wright, Aaron T and Renslow, Ryan S

Journal:

Journal of chemical information and modeling (2021): 481-492

Acupuncture improved lipid metabolism by regulating intestinal absorption in mice.

Authors:

Han, Jia and Guo, Xin and Meng, Xiang-Jin and Zhang, Jing and Yamaguchi, Reimon and Motoo, Yoshiharu and Yamada, Sohsuke

Journal:

World journal of gastroenterology (2020): 5118-5129

Development and validation of a chiral LC-MS method for the enantiomeric resolution of (+) and (-)-medetomidine in equine plasma by using polysaccharide-based chiral stationary phases.

Authors:

Karakka Kal, Abdul Khader and Nalakath, Jahfar and Kunhamu Karatt, Tajudheen and Perwad, Zubair and Mathew, Binoy and Subhahar, Michael

Journal:

Chirality (2020): 314-323

Olfactory marker protein directly buffers cAMP to avoid depolarization-induced silencing of olfactory receptor neurons.

Authors:

Nakashima, Noriyuki and Nakashima, Kie and Taura, Akiko and Takaku-Nakashima, Akiko and Ohmori, Harunori and Takano, Makoto

Journal:

Nature communications (2020): 2188

Physical properties

Solvent

DMSO

Storage, safety and handling

H-phrase	H303, H313, H333
Hazard symbol	XN
Intended use	Research Use Only (RUO)
R-phrase	R20, R21, R22
Storage	Freeze (< -15 °C); Minimize light exposure

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Page updated on May 9, 2026