Hydroxymethylglutaryl-CoA Lyase, Mitochondrial (HMGCL) Antibody

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Catalogue No: abx030051
Price: US$326.25
(Size: 80 µl)

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Datasheet SDS
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. [provided by RefSeq].

Target Hydroxymethylglutaryl-CoA Lyase, Mitochondrial (HMGCL)
Clonality Polyclonal
Reactivity Human
Tested Applications ELISA, WB
Host Rabbit
Recommended dilutions WB: 1/1000. Optimal dilutions/concentrations should be determined by the end user.
Conjugation Unconjugated
Immunogen KLH-conjugated synthetic peptide between 71-99 amino acids from the N-terminal region of human HMGCL.
Isotype IgG
Form Liquid
Purification Purified through a protein A column, followed by peptide affinity purification.
Storage Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
UniProt Primary AC P35914 (UniProt, ExPASy)
UniProt Secondary AC B4DUP4, B7UCC6, D3Y5K7, Q6IBC0, Q96FP8
UniProt Entry Name HMGCL_HUMAN
Gene Symbol HMGCL
KEGG hsa:3155
String 9606.ENSP00000363614
Molecular Weight Calculated MW: 34.4 kDa
Buffer PBS containing 0.09% sodium azide.
Availability Shipped within 5-10 working days.
Note This product is for research use only.
Research Articles on Hydroxymethylglutaryl-CoA Lyase, Mitochondrial (HMGCL)


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