Anti-Human HMGCS1 Polyclonal Antibody

HMG-CoA Synthase exists as both a mitochondrial (mHMGCS) and cytoplasmic (cHMGCS) enzyme that condenses acetyl-CoA with acetoacetyl-CoA to form HMG-CoA. The HMG-CoA produced by cHMGCS is transformed into mevalonate by HMG-CoA reductase, which starts isoprenoid biosynthesis. End products of the isoprenoid pathway include cholesterol, ubiquinone, dolichol, isopentenyl adenosine and farnesyl groups. mHMGCS, together with HMG-CoA Lyase, is responsible for ketone body biosynthesis. mHMGCS is expressed in liver and kidney. Fasting, cAMP and fatty acids increase the level of transcription of mHMGCS, while feeding and insulin repress it. A regulatory element within the mHMGCS promoter confers transcriptional regulation by PPAR, RXR, COUP-TF and HNF-4.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA10071
Size 100μl
Host Type Rabbit
Immunogen Synthetic peptide of human HMGCS1
Specificity
Isotype IgG
Reacitivity Human
Clone
Uniprot Q01581
Concentration 0.4 mg/mL
Dilution WB 1:500-1:2000, IHC 1:50-1:200
Formulation
Application WB,IHC,ELISA
Other Names 3 hydroxy 3 methylglutaryl Coenzyme A synthase 1 (soluble),3-hydroxy-3-methylglutaryl coenzyme A synthase,cytoplasmic,EC 2.3.3.10,HMCS1,HMG CoA synthase,HMG-CoA synthase,HMGCS,HMGCS1,Hydroxymethylglutaryl CoA synthase,cytoplasmic,Hydroxymethylglutaryl-CoA synthase,MGC90332
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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