{"product_id":"cst-95132t","title":"CST,  95132T, beta-Hydroxybutyryl Lysine (E6H5Q) Rabbit Monoclonal Antibody","description":"Monoclonal Antibody for studying . Validated for Western Blotting. Available in 2 sizes. Highly specific and rigorously validated in-house, beta-Hydroxybutyryl Lysine (E6H5Q) Rabbit Monoclonal Antibody (CST #95132) is ready to ship.\n\n\u003cb\u003eProduct Usage Information\u003c\/b\u003e\nWestern Blotting: 1:1000\n\u003cb\u003eStorage\u003c\/b\u003e\nSupplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg\/mL BSA, 50% glycerol, and less than 0.02% sodium azide. Store at -20°C. Do not aliquot the antibody.\n\u003cb\u003eProtocol\u003c\/b\u003e\nAvailable protocols: Western Blotting\n\u003cb\u003eSpecificity \/ Sensitivity\u003c\/b\u003e\nbeta-Hydroxybutyryl Lysine (E6H5Q) Rabbit Monoclonal Antibody recognizes a broad range of Î²-hydroxybutyryl lysine (Kbhb) containing proteins and peptides. This antibody does not cross-react with free Î²-hydroxybutyrate, and does not cross-react with peptides or proteins containing Î±-hydroxyisobutyrylated, acetylated, butyrylated, carboxymethylated, carboxyethylated, crotonylated, propionylated, or succinylated lysines.\nSpecies Reactivity: All Species Expected\n\u003cb\u003eSource \/ Purification\u003c\/b\u003e\nMonoclonal antibody is produced by immunizing animals with a synthetic peptide containing lysine Î²-hydroxybutyrylation flanked by degenerate amino acids at positions N- and C-terminal to the modified lysine.\n\u003cb\u003eBackground\u003c\/b\u003e\nLysine Î²-hydroxybutyrylation (Kbhb) is a reversible post-translational modification (PTM) that shares multiple regulatory enzymes with cellular acetylation machinery, including EP300 and HDAC1 (1).Â While acetylation is derived from acetyl-coenzyme-A (CoA), Î²-hydroxybutyrylation is derived from Î²-hydroxybutyryl-CoA, an intermediate generated from the metabolite Î²-hydroxybutyrate that is upregulated during nutrient limiting conditions such as starvation, ketogenic diets, and in diseases such as diabetes (2).Â The elucidation of the enzymes responsible for charging Î²-hydroxybutyrate with CoA to form Î²-hydroxybutyryl-CoA remains an active research area (3). Notable bhb-modified substrates identified through proteomic investigations include histones, as well as non-histone substrates such as FASN and TP53 (4-6). In models where cells are incubated with excess Î²-hydroxybutyrate to induce this PTM, protein sites displaying upregulated bhb levels differ from sites displaying upregulated acetylation levels, suggesting potential differences in Kbhb-induced pathways and crosstalk between distinct modification types.Â Â\n\n\u003cb\u003eSpecification\u003c\/b\u003e\n\nREACTIVITY: All\nSENSITIVITY: Endogenous\nSource\/Isotype: Rabbit IgG","brand":"CST","offers":[{"title":"Default Title","offer_id":46800238837929,"sku":"95132T","price":0.99,"currency_code":"USD","in_stock":true}],"url":"https:\/\/iright.com\/products\/cst-95132t","provider":"Iright","version":"1.0","type":"link"}