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AB258990

Human NDUFA6 knockout HeLa cell lysate

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NDUFA6 KO cell lysate available now. KO validated by. Free of charge wild type control included. Knockout achieved by using CRISPR/Cas9, 1 bp deletion in exon1 and 1 bp insertion in exon1.

View Alternative Names

B14, CI-B14, Complex I-B14, LYR motif-containing protein 6, LYRM6, NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 6 (14kD, B14), NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 6, 14kDa, NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 6, NADH-ubiquinone oxidoreductase 1 alpha subcomplex, 6, NADH-ubiquinone oxidoreductase B14 subunit, NADHB14, NDUA6_HUMAN, complex I B14 subunit

2 Images
Sanger Sequencing - Human NDUFA6 knockout HeLa cell lysate (AB258990)
  • Sanger seq

Unknown

Sanger Sequencing - Human NDUFA6 knockout HeLa cell lysate (AB258990)

Allele-1 : 1 bp deletion in exon1

Sanger Sequencing - Human NDUFA6 knockout HeLa cell lysate (AB258990)
  • Sanger seq

Unknown

Sanger Sequencing - Human NDUFA6 knockout HeLa cell lysate (AB258990)

Allele-2 : 1 bp insertion in exon1

Key facts

Cell type

HeLa

Species or organism

Human

Tissue

Cervix

Knockout validation

Sanger Sequencing

Mutation description

Knockout achieved by using CRISPR/Cas9, 1 bp deletion in exon1 and 1 bp insertion in exon1.

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, 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
NDUFA6
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.

The NDUFA6 protein also known as NADH:Ubiquinone Oxidoreductase Subunit A6 is an essential component of the mitochondrial respiratory chain complex I. Weighing approximately 15 kDa this protein forms a part of the inner mitochondrial membrane mainly expressed in tissues with high energy demands such as the heart brain and skeletal muscle. The protein aids in the initial steps of electron transfer from NADH to ubiquinone which is an important mechanical function in cellular respiration.
Biological function summary

NDUFA6 participates in the assembly and stability of complex I which is the largest of the five complexes in the mitochondrial electron transport chain. By contributing to complex I NDUFA6 plays a pivotal role in ATP production through oxidative phosphorylation. It ensures the effective transfer of electrons and maintains the proton gradient necessary for ATP synthesis. The integration of NDUFA6 within complex I illustrates its biological necessity for proper cellular energy metabolism.

Pathways

NDUFA6 significantly impacts the oxidative phosphorylation pathway and mitochondrial complex I assembly pathway. Its interaction within these pathways influences the overall energy metabolism and cellular respiration efficiency. The protein engages with several partners including NDUFS2 and NDUFV1 which are also integral subunits of complex I. These interactions highlight how NDUFA6 tightly coordinates with other proteins to ensure optimal energy production.

Defects in NDUFA6 have been associated with mitochondrial diseases such as Leber Hereditary Optic Neuropathy and mitochondrial complex I deficiency. These conditions lead to impaired energy metabolism affecting tissues with high energy demands. In these diseases interactions with proteins like NDUFS1 and other complex I subunits become altered disrupting normal mitochondrial function. Understanding these connections emphasizes the importance of NDUFA6 in maintaining mitochondrial health and cellular energy balance.

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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