Name: Crotonaldehyde BSA Conjugate
Brand: AAT Bioquest
SKU: 16070
Price: 332 USD
Availability: InStock

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.

General packaging for Cat. No. 16070. Your actual packaging may differ.

Protocol

SDS

COA

Catalog	Size	Price	Quantity
16070	100 ug	Price

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

Physical properties

Solvent

Water

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
UNSPSC	12171501

Documents

Protocol
Safety Data Sheet
Certificate of Analysis

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Page updated on October 19, 2025