Crotonaldehyde BSA Conjugate
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Additional ordering information
Telephone | 1-800-990-8053 |
Fax | 1-800-609-2943 |
sales@aatbio.com | |
International | See distributors |
Bulk request | Inquire |
Custom size | Inquire |
Shipping | Standard overnight for United States, inquire for international |
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 |
Related products
Overview | SDSProtocol |
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
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
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
Authors: Reiter, Maud and Torssell, Staffan and Lee, Sandra and Macmillan, David W C
Journal: Chemical science (2010): 37-42
Nucleophilic carbenes as organocatalysts.
Authors: Glorius, F and Hirano, K
Journal: Ernst Schering Foundation symposium proceedings (2007): 159-81
Authors: Glorius, F and Hirano, K
Journal: Ernst Schering Foundation symposium proceedings (2007): 159-81
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
Authors: Seiner, Derrick R and LaButti, Jason N and Gates, Kent S
Journal: Chemical research in toxicology (2007): 1315-20
Coupling products of nucleosides with the glyoxal adduct of deoxyguanosine.
Authors: Brock, Angela K and Kozekov, Ivan D and Rizzo, Carmelo J and Harris, Thomas M
Journal: Chemical research in toxicology (2004): 1047-56
Authors: Brock, Angela K and Kozekov, Ivan D and Rizzo, Carmelo J and Harris, Thomas M
Journal: Chemical research in toxicology (2004): 1047-56
Structural and kinetic determinants of aldehyde reduction by aldose reductase.
Authors: Srivastava, S and Watowich, S J and Petrash, J M and Srivastava, S K and Bhatnagar, A
Journal: Biochemistry (1999): 42-54
Authors: Srivastava, S and Watowich, S J and Petrash, J M and Srivastava, S K and Bhatnagar, A
Journal: Biochemistry (1999): 42-54
Inhibition of glutathione S-transferase activity in human melanoma cells by alpha,beta-unsaturated carbonyl derivatives. Effects of acrolein, cinnamaldehyde, citral, crotonaldehyde, curcumin, ethacrynic acid, and trans-2-hexenal.
Authors: Iersel, M L and Ploemen, J P and Struik, I and van Amersfoort, C and Keyzer, A E and Schefferlie, J G and van Bladeren, P J
Journal: Chemico-biological interactions (1996): 117-32
Authors: Iersel, M L and Ploemen, J P and Struik, I and van Amersfoort, C and Keyzer, A E and Schefferlie, J G and van Bladeren, P J
Journal: Chemico-biological interactions (1996): 117-32
Application notes
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FAQ
How can I lyse my cells without lysing the nuclear membrane?
What are the differences between calcium ion indicators: Cal 520, Cal 520FF, and Cal 520N?
How do I make an AM ester stock solution?
Can we fix cells with glutaraldehyde and then stain with fluorescent phalloidin?
What is the difference between FluoroQuest Anti-fading Kit I and FluoroQuest Anti-fading Kit II?
What are the differences between calcium ion indicators: Cal 520, Cal 520FF, and Cal 520N?
How do I make an AM ester stock solution?
Can we fix cells with glutaraldehyde and then stain with fluorescent phalloidin?
What is the difference between FluoroQuest Anti-fading Kit I and FluoroQuest Anti-fading Kit II?