OXCT1 antibody
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Description
This gene encodes a member of the 3-oxoacid CoA-transferase gene family. The encoded protein is a homodimeric mitochondrial matrix enzyme that plays a central role in extrahepatic ketone body catabolism by catalyzing the reversible transfer of coenzyme A from succinyl-CoA to acetoacetate. Mutations in this gene are associated with succinyl CoA:3-oxoacid CoA transferase deficiency.
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Product specifications
| Category | Primary Antibodies |
| Immunogen Target | 3-oxoacid CoA transferase 1 (OXCT1) |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Recommended Dilution | WB: 1:500 - 1:2000; IHC: 1:50 - 1:200; IF: 1:50 - 1:200 |
| Clonality | polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Observed MW | 56 kDa |
| Purity | ≥95% as determined by SDS-PAGE |
| Purification | Immunogen affinity purified |
| Size 1 | 100µg |
| Form | liquid |
| Tested Applications | ELISA, WB, IHC, IF |
| Storage | PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months (Avoid repeated freeze / thaw cycles.) |
| UniProt ID | P55809 |
| Gene ID | 5019 |
| Alias | Succinyl-CoA:3-ketoacid coenzyme A transferase 1, mitochondrial (SCOT),3-oxoacid CoA-transferase 1,Somatic-type succinyl-CoA:3-oxoacid CoA-transferase (SCOT-s),Succinyl-CoA:3-oxoacid CoA transferase,OXCT1,OXCT,SCOT |
| Background | Antibody anti-OXCT1 |
| Status | RUO |
| Note | Mol. Weight 56 kDa |
Descripción
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Human OXCT1 (3-oxoacid CoA-transferase 1) ELISA Kit
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OXCT1 antibody
This gene encodes a member of the 3-oxoacid CoA-transferase gene family. The encoded protein is a homodimeric mitochondrial matrix enzyme that plays a central role in extrahepatic ketone body catabolism by catalyzing the reversible transfer of coenzyme A from succinyl-CoA to acetoacetate. Mutations in this gene are associated with succinyl CoA:3-oxoacid CoA transferase deficiency.
Ver ProductoOXCT1 antibody
This gene encodes a member of the 3-oxoacid CoA-transferase gene family. The encoded protein is a homodimeric mitochondrial matrix enzyme that plays a central role in extrahepatic ketone body catabolism by catalyzing the reversible transfer of coenzyme A from succinyl-CoA to acetoacetate. Mutations in this gene are associated with succinyl CoA:3-oxoacid CoA transferase deficiency.
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