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AB258826

Human COX7A2 knockout HEK-293T cell lysate

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COX7A2 KO cell lysate available now. KO validated by. Free of charge wild type control included. Knockout achieved by using CRISPR/Cas9, 1 bp insertion in exon 1 and Insertion of the selection cassette in exon 1.

View Alternative Names

COX7AL, COX7AL1, COXVIIa L, CX7A2_HUMAN, Cytochrome c oxidase polypeptide 7A2 mitochondrial, Cytochrome c oxidase polypeptide VIIa liver/heart, Cytochrome c oxidase subunit 7A2, Cytochrome c oxidase subunit 7A2 mitochondrial, Cytochrome c oxidase subunit VIIa polypeptide 2, Cytochrome c oxidase subunit VIIa-L, Cytochrome c oxidase subunit VIIa-liver/heart, Hepatic cytochrome c oxidase chain VIIa, MGC118950, MGC118951, MGC118952, MGC126875, MGC126877, VIIAL, mitochondrial

2 Images
Sanger Sequencing - Human COX7A2 knockout HEK-293T cell lysate (AB258826)
  • Sanger seq

Unknown

Sanger Sequencing - Human COX7A2 knockout HEK-293T cell lysate (AB258826)

Allele-2 : Insertion of the selection cassette in exon 1

Sanger Sequencing - Human COX7A2 knockout HEK-293T cell lysate (AB258826)
  • Sanger seq

Unknown

Sanger Sequencing - Human COX7A2 knockout HEK-293T cell lysate (AB258826)

Allele-1 : 1 bp insertion in exon 1

Key facts

Cell type

HEK-293T

Species or organism

Human

Tissue

Kidney

Knockout validation

Sanger Sequencing

Mutation description

Knockout achieved by using CRISPR/Cas9, 1 bp insertion in exon 1 and Insertion of the selection cassette in exon 1.

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, ERS Genomics Limited and Sigma-Aldrich Co. LLC, and is developed with patented technology. For full details of the licenses and patents please refer to our limited use license and patent pages.

What's included?

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Properties and storage information

Gene name
COX7A2
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.

COX7A2 also known as cytochrome c oxidase subunit 7A2 is a component of the cytochrome c oxidase complex found in the inner mitochondrial membrane. This protein has an approximate molecular mass of 9.8 kDa. COX7A2 is expressed in various tissues with notable expression in highly metabolic tissues such as the heart and skeletal muscle. It plays a role in the electron transport chain by participating in the reduction of oxygen to water.
Biological function summary

COX7A2 contributes to the cytochrome c oxidase (complex IV) of the mitochondrial electron transport chain. This complex is important for ATP production through oxidative phosphorylation. COX7A2 forms part of the multi-subunit complex that facilitates efficient transfer of electrons which is essential for mitochondrial energy production. Its function in this complex underlines its importance in maintaining cellular respiration and energy homeostasis.

Pathways

COX7A2 plays an important role in the mitochondrial oxidative phosphorylation pathway. This pathway is essential for ATP production in eukaryotic cells. Another significant pathway involving COX7A2 is the respiratory electron transport pathway. Within these pathways COX7A2 interacts with other cytochrome c oxidase subunits like COX4 and COX5A which help regulate electron transfer and influence overall metabolic activity.

COX7A2 alterations and dysfunctions have been associated with mitochondrial disorders and myopathies. These disorders are often characterized by impaired energy metabolism due to defective oxidative phosphorylation. Within this context changes in COX7A2 expression can influence the functions of other cytochrome c oxidase subunits potentially affecting mitochondrial function and contributing to the pathological state of diseases like mitochondrial encephalomyopathy.

Quality control

STR analysis

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

Cell culture

Biosafety level

EU: 2 US: 2

Adherent/suspension

Adherent

Gender

Female

Product protocols

Product promise

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For full details, please see our Terms & Conditions

Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.

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