Anti-Human/Mouse/Rat HMGCL Polyclonal Antibody

The protein encoded by this gene belongs to the HMG-CoA lyase family. It is a mitochondrial enzyme that catalyzes the final step of leucine degradation and plays a key role in ketone body formation. Mutations in this gene are associated with HMG-CoA lyase deficiency. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. 
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Properties

Data Sheet Click for Datasheet
Catalog Number PA12034
Size 100μl
Host Type Rabbit
Immunogen Recombinant protein of human HMGCL
Specificity Fibroblasts, liver and lymphoblasts.
Isotype IgG
Reacitivity Human,Mouse,Rat
Clone
Uniprot P35914
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 CoA lyase,3 hydroxy 3 methylglutaryl Coenzyme A lyase,3 hydroxymethyl 3 methylglutaryl Coenzyme A lyase (hydroxymethylglutaricaciduria),3 hydroxymethyl 3 methylglutaryl Coenzyme A lyase,3-hydroxy-3-methylglutarate-CoA lyase,HL,HMG CoA lyase,HMG CoA Lyase Deficiency,HMG-CoA lyase,HMGCL,HMGCL,Hydroxymethylglutaricaciduria,Hydroxymethylglutaryl CoA lyase,Hydroxymethylglutaryl CoA lyase mitochondrial,Hydroxymethylglutaryl-CoA lyase,Mitochondrial 3 hydroxy 3 methylglutaryl CoA lyase,mitochondrial,MS725,OTTHUMP00000044830
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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