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>   home   >   Products   >   Peptides   >   Blocking Peptides   >   CBR4 Antibody (C-term) Blocking Peptide   

CBR4 Antibody (C-term) Blocking Peptide

Synthetic peptide

     
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Product Information
Primary Accession Q8N4T8
Clone Names 110808094
Peptide ID 110808094
Additional Information
Gene ID 84869
Other Names Carbonyl reductase family member 4, 1---, 3-oxoacyl-[acyl-carrier-protein] reductase, 111-, Quinone reductase CBR4, CBR4
Format Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 1 mg/ml.
StorageMaintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C.
PrecautionsThis product is for research use only. Not for use in diagnostic or therapeutic procedures.
Protein Information
Name CBR4
Synonyms SDR45C1
Function The heterotetramer with HSD17B8 has NADH-dependent 3- ketoacyl-acyl carrier protein reductase activity, and thereby plays a role in mitochondrial fatty acid biosynthesis (PubMed:19571038, PubMed:25203508). Within the heterotetramer, HSD17B8 binds NADH; CBR4 binds NADPD (PubMed:25203508). The homotetramer has NADPH-dependent quinone reductase activity (PubMed:19000905). Both homotetramer and the heterotetramer have broad substrate specificity and can reduce 9,10- phenanthrenequinone, 1,4-benzoquinone and various other o-quinones and p-quinones (in vitro) (PubMed:19000905, PubMed:19571038, PubMed:25203508).
Cellular Location Mitochondrion matrix
Tissue Location Detected in liver and kidney (at protein level).
Research Areas
Citations (0)

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Background

The heteroteramer with HSD17B8 has NADH-dependent 3-ketoacyl-acyl carrier protein reductase activity. May play a role in biosynthesis of fatty acids in mitochondria. The homotetramer may act as NADPH-dependent quinone reductase. Has broad substrate specificity and reduces 9,10-phenanthrenequinone, 1,4-benzoquinone and various other o-quinones and p-quinones (in vitro).

References

Chen, Z., et al. FASEB J. 23(11):3682-3691(2009)Persson, B., et al. Chem. Biol. Interact. 178 (1-3), 94-98 (2009) :Endo, S., et al. Biochem. Biophys. Res. Commun. 377(4):1326-1330(2008)Lamesch, P., et al. Genomics 89(3):307-315(2007)

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$ 80.00
Cat# BP17512b
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