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- Ab04118-23.0 Anti-1,3-diketone hapten [33F12]
- Species independent
- Rabbit IgG
- Purified
- Ships in 5-6 weeks
- Ab04118-2.0 Anti-1,3-diketone hapten [33F12]
- Species independent
- Mouse IgG2a
- Purified
- Ships in 5-6 weeks
Recombinant monoclonal antibody to 1,3-diketone hapten. Manufactured using AbAb’s Recombinant Platform with variable regions (i.e. specificity) from the hybridoma 33F12.
Alternative Name(s) of Target: Hapten 1,3-diketone; β-keto acids; beta keto acids
Immunogen: The original antibody was generated by immunizing GIX+ mice with a keyhole limpet hemocyanin (KLH)-coupled diketone hapten.
Specificity: This antibody was raised against 1,3-diketone hapten, but it is capable of catalyzing the decarboxylation of structurally related β-keto acids.
Application Notes: This antibody efficiently catalyzes aldol and retro-aldol reactions and covalently binds 1,3-diketone hapten. The (kcat/KM)/kuncat is approximately 109 at pH 7.5 as measured by the consumption of substrates and production of aldol products (monitored using reversed-phase high-performance liquid chromatography (HPLC) and enzymatic assays) (Wagner et al., 1995; PMID: 8525368). This antibody efficiently catalyzed the decarboxylation of two hapten-related β-keto acids (marked 4 and 5 in scheme 1 in the publication) with significant rate enhancements (kcat/kuncat) of 4959 and 11,261, respectively (Björnestedt et al., 1996). The crystallization of the Fab version of this antibody revealed a binding pocket characterized by a narrow, elongated cleft, where the catalytic lysine residue is prominently located (Barbas III et al., 1997; PMID: 9405338).
Antibody first published in:
Wagner et al. Efficient aldolase catalytic antibodies that use the enamine mechanism of natural enzymes Science. 1995 Dec 15;270(5243):1797-800. doi: 10.1126/science.270.5243.1797 PMID:8525368
Note on publication:
The original publication describes the generation of efficient aldolase catalytic antibodies that utilize the enamine mechanism of natural enzymes, mimicking their catalytic process and exhibiting diastereofacial selectivity in the aldol reaction.