logo
AAT Bioquest

Crotonaldehyde BSA Conjugate

Crotonaldehyde is a common environmental pollutant. Inhalation of tobbacco smoke is a significant source of crotonaldehyde, exposing smokers to 30−170 μg/kg/day. Crotonaldehyde also occurs naturally in certain fruits and vegetables, selected dairy products, and some alcoholic beverages. In addition to these exogenous sources, crotonaldehyde is also formed endogenously during lipid peroxidation (LPO), a factor that may contribute to the aldehydes' presence in the serum of nonsmokers. As with other unsaturated aldehydes, crotonaldehyde exhibits many toxicological properties, including an ability to cause multi-organ toxicity in laboratory animals; DNA damage and mutagenicity in vitro; and carcinogenicity in vivo. Crotonaldehyde BSA conjugate was carefully prepared from the addition of crotonaldehyde to bovine serum albumin (BSA). Our crotonaldehyde BSA conjugate is fully characterized with the defined ratio of crotonaldehyde/protein that is not provided by other vendors. It has been used for preparing anti-crotonaldehyde antibodies and for developing crotonaldehyde-quantifying assays.

References

View all 8 references: Citation Explorer
Mercapturic Acids Derived from the Toxicants Acrolein and Crotonaldehyde in the Urine of Cigarette Smokers from Five Ethnic Groups with Differing Risks for Lung Cancer.
Authors: Park, Sungshim L and Carmella, Steven G and Chen, Menglan and Patel, Yesha and Stram, Daniel O and Haiman, Christopher A and Le Marchand, Loic and Hecht, Stephen S
Journal: PloS one (2015): e0124841
Tandem catalysis in domino olefin cross-metathesis/intramolecular oxa-conjugate cyclization: concise synthesis of 2,6-cis-substituted tetrahydropyran derivatives.
Authors: Fuwa, Haruhiko and Noguchi, Takuma and Noto, Kenkichi and Sasaki, Makoto
Journal: Organic & biomolecular chemistry (2012): 8108-12
The organocatalytic three-step total synthesis of (+)-frondosin B.
Authors: Reiter, Maud and Torssell, Staffan and Lee, Sandra and Macmillan, David W C
Journal: Chemical science (2010): 37-42
Kinetics and mechanism of protein tyrosine phosphatase 1B inactivation by acrolein.
Authors: Seiner, Derrick R and LaButti, Jason N and Gates, Kent S
Journal: Chemical research in toxicology (2007): 1315-20
Nucleophilic carbenes as organocatalysts.
Authors: Glorius, F and Hirano, K
Journal: Ernst Schering Foundation symposium proceedings (2007): 159-81
Page updated on December 17, 2024

Ordering information

Price
Unit size
Catalog Number16070
Quantity
Add to cart

Additional ordering information

Telephone1-800-990-8053
Fax1-800-609-2943
Emailsales@aatbio.com
InternationalSee distributors
Bulk requestInquire
Custom sizeInquire
Technical SupportContact us
Purchase orderSend to sales@aatbio.com
ShippingStandard overnight for United States, inquire for international
Request quotation

Physical properties

Solvent

Water

Storage, safety and handling

H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22

Storage

Freeze (< -15 °C); Minimize light exposure
UNSPSC12171501