HPA012047

Anti-OXCT1 antibody produced in rabbit

Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution

Manufacturer: Sigma Aldrich

Synonym(S): Anti-3-oxoacid-CoA transferase 1, Anti-Scot-S, Anti-Somatic-type succinyl CoA:3-oxoacid CoA-transferase, Anti-Succinyl-CoA:3-ketoacid-coenzyme A transferase 1, mitochondrial

Select a Size

Pack Size SKU Availability Price
100 μL HPA012047-100-μL In Stock ₹ 48,995.40

HPA012047 - 100 μL

₹ 48,995.40

In Stock

Quantity

1

Base Price: ₹ 48,995.40

GST (18%): ₹ 8,819.172

Total Price: ₹ 57,814.572

biological source

rabbit

Quality Level

100

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

product line

Prestige Antibodies® Powered by Atlas Antibodies

form

buffered aqueous glycerol solution

species reactivity

human, mouse, rat

enhanced validation

orthogonal RNAseqindependentLearn more about Antibody Enhanced Validation

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Description

  • Immunogen: Succinyl-CoA:3-ketoacid-coenzyme A transferase 1, mitochondrial Precursor recombinant protein epitope signature tag (PrEST)
  • Application: Anti-OXCT1 antibody produced in rabbit, a Prestige Antibody, is developed and validated by the Human Protein Atlas (HPA) project . Each antibody is tested by immunohistochemistry against hundreds of normal and disease tissues. These images can be viewed on the Human Protein Atlas (HPA) site by clicking on the Image Gallery link. The antibodies are also tested using immunofluorescence and western blotting. To view these protocols and other useful information about Prestige Antibodies and the HPA, visit sigma.com/prestige.
  • Biochem/physiol Actions: OXCT1 (3-oxoacid CoA transferase 1) is a mitochondrial ketolytic enzyme involved in the ketone metabolism. It facilitates the conversion of coenzyme A from succinyl-coenzyme A to acetoacetate for the generation of acetoacetyl-CoA. It has been reported that the transfer reaction may utilize glucose for the energy requirement. Missense mutations in OXCT1 cause succinyl CoA:3-oxoacid CoA transferase deficiency.
  • Features and Benefits: Prestige Antibodies® are highly characterized and extensively validated antibodies with the added benefit of all available characterization data for each target being accessible via the Human Protein Atlas portal linked just below the product name at the top of this page. The uniqueness and low cross-reactivity of the Prestige Antibodies® to other proteins are due to a thorough selection of antigen regions, affinity purification, and stringent selection. Prestige antigen controls are available for every corresponding Prestige Antibody and can be found in the linkage section.Every Prestige Antibody is tested in the following ways:IHC tissue array of 44 normal human tissues and 20 of the most common cancer type tissues.Protein array of 364 human recombinant protein fragments.
  • Linkage: Corresponding Antigen APREST70201
  • Physical form: Solution in phosphate-buffered saline, pH 7.2, containing 40% glycerol and 0.02% sodium azide
  • Legal Information: Prestige Antibodies is a registered trademark of Merck KGaA, Darmstadt, Germany
  • Disclaimer: Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

SAFETY INFORMATION

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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