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AB258777

Human ACOX3 knockout HeLa cell lysate

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ACOX3 KO cell lysate available now. KO validated. Free of charge wild type control included. Knockout achieved by using CRISPR/Cas9, 16 bp deletion in exon5 and 5 bp deletion in exon5.
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Sanger Sequencing - Human ACOX3 knockout HeLa cell lysate (AB258777)
  • Sanger seq

Unknown

Sanger Sequencing - Human ACOX3 knockout HeLa cell lysate (AB258777)

Allele-2 : 5 bp deletion in exon5

Sanger Sequencing - Human ACOX3 knockout HeLa cell lysate (AB258777)
  • Sanger seq

Unknown

Sanger Sequencing - Human ACOX3 knockout HeLa cell lysate (AB258777)

Allele-1 : 16 bp deletion in exon5

Key facts

Cell type

HeLa

Species or organism

Human

Tissue

Cervix

Knockout validation

Sanger Sequencing

Mutation description

Knockout achieved by using CRISPR/Cas9, 16 bp deletion in exon5 and 5 bp deletion in exon5.

Disease

Adenocarcinoma

Product details

Knockout cell lysate achieved by CRISPR/Cas9.

REACH authorisation
Abcam has not and does not intend to apply for the REACH Authorisation of customers' uses of products that contain European Authorisation list (Annex XIV) substances.
It is the responsibility of our customers to check the necessity of application of REACH Authorisation, and any other relevant authorisations, for their intended uses.

Lysate preparation: Our lysates are made using RIPA buffer to which we add a protease inhibitor cocktail and phosphatase inhibitor cocktail (ratio: 300:100:10). This means that the protein of interest is denatured. If you require a native form of the protein please use the live cell version. Please refer to our lysis protocol for further details on how our lysates are prepared.

User storage instructions: Lyophilizate may be stored at 4°C. After reconstitution, store at -20°C for short-term storage or -80°C for long-term storage.

This product is subject to limited use licenses from The Broad Institute and ERS Genomics Limited, and is developed with patented technology. For full details of the limited use licenses and relevant patents please refer to our limited use license and patent pages.

What's included?

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Properties and storage information

Gene name
ACOX3
Gene editing type
Knockout
Gene editing method
CRISPR technology
Knockout validation
Sanger Sequencing
Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

ACOX3 also known as acyl-CoA oxidase 3 or PRACOX3 is an enzyme that functions in the peroxisomal beta-oxidation of branched-chain fatty acids. It specifically catalyzes the first oxidation step introducing a double bond between alpha and beta carbon of Acyl-CoA esters. ACOX3 has a molecular mass of approximately 75 kDa. Expression of ACOX3 primarily occurs in liver and kidney tissues where it plays a significant role in lipid metabolism.
Biological function summary

ACOX3 contributes to the breakdown of pristanic acid a branched-chain fatty acid derived from phytanic acid. It functions as part of a peroxisomal enzyme system that efficiently oxidizes fatty acids that contain branches on their carbon chains which mitochondria can’t oxidize. ACOX3 works alongside other enzymes like ACOX1 and ACOX2 which oxidize different substrates ensuring a specialized fatty acid metabolism in the cell.

Pathways

ACOX3 plays a critical role in the peroxisomal fatty acid beta-oxidation pathway also contributing to the catabolism of very-long-chain fatty acids. This pathway complements the mitochondrial beta-oxidation providing a synergistic approach for complete fatty acid degradation. ACOX3 works closely related to proteins like peroxisomal bifunctional enzyme and thiolase completing the sequential steps necessary for beta-oxidation and energy production from fatty acids.

Mutations or dysfunctions in ACOX3 can lead to disruptions in fatty acid metabolism particularly affecting the metabolism of branched-chain fatty acids and potentially contributing to conditions such as Refsum disease or Zellweger syndrome. These disorders often exhibit accumulation of toxic metabolites causing harmful effects in tissues. They link ACOX3 dysfunction to broader peroxisomal biogenesis issues that involve other enzymes such as the PEX proteins which are vital for normal peroxisomal function and maintenance.

Quality control

STR analysis

D5S818, TH01, D16S539, TPOX, CSF1PO, D13S317, D7S820

Cell culture

Biosafety level

EU: 2 US: 2

Adherent/suspension

Adherent

Gender

Female

Product protocols

Product promise

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