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AB263103

Human ATP5G2 knockout HEK-293T cell lysate

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ATP5MC2 KO cell lysate available now. KO validated. Free of charge wild type control included. Knockout achieved by using CRISPR/Cas9, Homozygous: 1 bp insertion in exon 2.
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Sanger Sequencing - Human ATP5G2 knockout HEK-293T cell lysate (AB263103)
  • Sanger seq

Unknown

Sanger Sequencing - Human ATP5G2 knockout HEK-293T cell lysate (AB263103)

Homozygous : 1 bp insertion in exon 2

Key facts

Cell type

HEK-293T

Species or organism

Human

Tissue

Kidney

Knockout validation

Sanger Sequencing

Mutation description

Knockout achieved by using CRISPR/Cas9, Homozygous: 1 bp insertion in exon 2.

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Complementary Products

Cell Lines & Lysates

AB266394

Human ATP5G2 knockout HEK-293T cell line

Sanger Sequencing - Human ATP5G2 knockout HEK-293T cell line (AB266394)

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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.

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What's included?

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Properties and storage information

Gene name
ATP5MC2
Gene editing type
Knockout
Gene editing method
CRISPR technology
Knockout validation
Sanger Sequencing
Zygosity
Homozygous
Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C
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Supplementary information

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

ATP5G2 also known as ATP synthase subunit c mitochondrial 2 plays a mechanical role in the production of ATP. This protein functions as a component of the Fo subunit of ATP synthase which operates in the mitochondrial membrane. ATP5G2 has a mass of approximately 8.2 kDa and appears in tissues with high energy demand like muscle and nerve cells. The protein's primary role is to facilitate proton translocation across the mitochondrial membrane important for ATP synthesis.
Biological function summary

ATP5G2 contributes to the generation of cellular energy by being part of the ATP synthase complex also called Complex V of the mitochondrial electron transport chain. This complex performs oxidative phosphorylation converting ADP and inorganic phosphate into ATP which fuels various cellular processes. The subunit's function within the complex directly impacts cellular energy yields and efficiency. Its interaction with other ATP synthase subunits is vital for maintaining the function of the entire complex.

Pathways

ATP5G2 integrates into the oxidative phosphorylation pathway which is central to energy metabolism. This pathway is important for the conversion of nutrients into usable energy. ATP5G2 works closely with the NADH dehydrogenase complex (Complex I) to enable effective electron transport and subsequent ATP generation. The intricate coordination between these complexes is necessary for the maintenance of the mitochondrial membrane potential and overall cellular energetics.

Mutations or dysfunction in ATP5G2 can link to mitochondrial disorders such as Leigh syndrome which involves neurodegeneration and energy deficits. The protein's malfunction can disrupt ATP synthesis affecting the energy balance in cells particularly those requiring high ATP levels. Additionally ATP5G2 might contribute to metabolic disorders like diabetes where insulin secretion and action depend on proper energy metabolism. The role of ATP5G2 alongside other ATP synthase subunits highlights its importance in maintaining mitochondrial and cellular function.
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Quality control

STR analysis

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

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Cell culture

Biosafety level

EU: 2 US: 2

Adherent/suspension

Adherent

Gender

Female

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Product protocols

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Product promise

We are committed to supporting your work with high-quality reagents, and we're here for you every step of the way. In the unlikely event that one of our products does not perform as expected, you're protected by our Product Promise.
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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