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AB263099

Human ATP10A knockout A549 cell lysate

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ATP10A 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 exon2 and 4 bp deletion in exon2.

View Alternative Names

AT10A_HUMAN, ATP10A, ATP10C, ATPVA, ATPVC, ATPase Class V type 10C, ATPase class V type 10A, ATPase type IV phospholipid transporting (P type), Aminophospholipid translocase VA, KIAA0566, Phospholipid transporting ATPase VA, Probable phospholipid-transporting ATPase VA

2 Images
Sanger Sequencing - Human ATP10A knockout A549 cell lysate (AB263099)
  • Sanger seq

Unknown

Sanger Sequencing - Human ATP10A knockout A549 cell lysate (AB263099)

Allele-1 : 4 bp deletion in exon2

Sanger Sequencing - Human ATP10A knockout A549 cell lysate (AB263099)
  • Sanger seq

Unknown

Sanger Sequencing - Human ATP10A knockout A549 cell lysate (AB263099)

Allele-2 : 1 bp insertion in exon2

Key facts

Cell type

A549

Species or organism

Human

Tissue

Lung

Knockout validation

Sanger Sequencing

Mutation description

Knockout achieved by using CRISPR/Cas9, 1 bp insertion in exon2 and 4 bp deletion in exon2.

Disease

Carcinoma

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
ATP10A
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.

ATP10A also known as ATPase Class V type 10A is a protein involved in phospholipid transport. This protein is part of the P-type ATPase family characterized by its ability to catalyze ATP hydrolysis providing the energy needed for the transport of lipids across cell membranes. ATP10A has an approximate mass of 125 kDa. Expression of ATP10A occurs in various tissues with a higher concentration noted in the brain and adipose tissue.
Biological function summary

ATP10A contributes to maintaining the asymmetrical distribution of phospholipids in the cell membrane which is essential for cell function and integrity. This protein does not function alone; it associates with CDC50 to form a heterodimer complex important for its lipid translocase activity. This activity helps maintain cellular homeostasis impacting processes such as apoptosis and membrane curvature necessary for cell signaling and vesicle formation.

Pathways

The functional role of ATP10A integrates into lipid metabolism and cellular signaling pathways. ATP10A significantly impacts the phospholipid translocation pathway which regulates membrane dynamics and is associated with apoptosis-related proteins like scramblases. Within these pathways ATP10A also interacts with PI3K/AKT a signaling pathway important for cellular growth survival and metabolism.

ATP10A holds importance in neurological and metabolic diseases. Altered expression or mutations in ATP10A appear linked to neurodevelopmental conditions such as Angelman syndrome where an imbalance in phospholipid transport may contribute to pathogenesis. Furthermore ATP10A associates with obesity-related disorders where its role in lipid metabolism links it to proteins like leptin which regulate energy balance and fat storage.

Quality control

STR analysis

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

Cell culture

Biosafety level

EU: 1 US: 1

Adherent/suspension

Adherent

Gender

Male

Product protocols

Product promise

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For full details, please see our Terms & Conditions

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