Human ACADSB Protein

Product Description

Human ACADSB Protein
Catalog number: B2011473
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 50 µg
Molecular Weight or Concentration: 0.5 mg/mL
Supplied as: Solution
Applications: molecular tool for various biochemical applications
Storage: -20 °C
Keywords: ACADSB protein (His tag), ACAD7 protein, mitochondrial protein, SBCAD protein, 2-MEBCAD protein, Short/branched chain specific acyl-CoA dehydrogenase protein
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

References:
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2: Kamide K, Kokubo Y, Yang J, Matayoshi T, Inamoto N, Takiuchi S, Horio T, Miwa Y, Yoshii M, Tomoike H, Tanaka C, Banno M, Okuda T, Kawano Y, Miyata T. Association of genetic polymorphisms of ACADSB and COMT with human hypertension J Hypertens. 2007 Jan;25(1):103-10.
3: Lu D, Yang Z, Xia Q, Gao S, Sun S, Luo X, Li Z, Zhang X, Li X. ACADSB regulates ferroptosis and affects the migration, invasion, and proliferation of colorectal cancer cells Cell Biol Int. 2020 Nov;44(11):2334-2343.
4: Arden KC, Viars CS, Fu K, Rozen R. Localization of short/branched chain acyl-CoA dehydrogenase (ACADSB) to human chromosome 10 Genomics. 1995 Feb 10;25(3):743-5.
5: Rozen R, Vockley J, Zhou L, Milos R, Willard J, Fu K, Vicanek C, Low-Nang L, Torban E, Fournier B. Isolation and expression of a cDNA encoding the precursor for a novel member (ACADSB) of the acyl-CoA dehydrogenase gene family Genomics. 1994 Nov 15;24(2):280-7.
6: Key J, Torres-Odio S, Bach NC, Gispert S, Koepf G, Reichlmeir M, West AP, Prokisch H, Freisinger P, Newman WG, Shalev S, Sieber SA, Wittig I, Auburger G. Inactivity of Peptidase ClpP Causes Primary Accumulation of Mitochondrial Disaggregase ClpX with Its Interacting Nucleoid Proteins, and of mtDNA Cells. 2021 Nov 29;10(12):3354.
7: Alfardan J, Mohsen AW, Copeland S, Ellison J, Keppen-Davis L, Rohrbach M, Powell BR, Gillis J, Matern D, Kant J, Vockley J. Characterization of new ACADSB gene sequence mutations and clinical implications in patients with 2-methylbutyrylglycinuria identified by newborn screening Mol Genet Metab. 2010 Aug;100(4):333-8.
8: Korman SH. Inborn errors of isoleucine degradation: a review Mol Genet Metab. 2006 Dec;89(4):289-99.
9: Sass JO, Ensenauer R, Röschinger W, Reich H, Steuerwald U, Schirrmacher O, Engel K, Häberle J, Andresen BS, Mégarbané A, Lehnert W, Zschocke J. 2-Methylbutyryl-coenzyme A dehydrogenase deficiency: functional and molecular studies on a defect in isoleucine catabolism Mol Genet Metab. 2008 Jan;93(1):30-5.
10: Liu J, Liu H, Zhao Z, Wang J, Guo D, Liu Y. Regulation of Actg1 and Gsta2 is possible mechanism by which capsaicin alleviates apoptosis in cell model of 6-OHDA-induced Parkinson’s disease Biosci Rep. 2020 Jun 26;40(6):BSR20191796.

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