Description
Key facts
Cell type:HeLa,
Species or organism:Human,
Tissue:Cervix,
Form:LiquidSee storage information,
Knockout validation:Sanger Sequencing,
Mutation description:Knockout achieved by using CRISPR/Cas9, Homozygous: 7 bp deletion in exon 1,
Disease:Adenocarcinoma
Product details:
We will provide viable cells that proliferate on revival.
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
patent pages
Properties and Storage Information:
Gene name-ANKRD13A, Gene editing type-Knockout, Gene editing method-CRISPR technology, Knockout validation-Sanger Sequencing, Zygosity-Homozygous, Shipped at conditions-Dry Ice, Appropriate short-term storage conditions--196°C, Appropriate long-term storage conditions--196°C
Supplementary Information:
This supplementary information is collated from multiple sources and compiled automatically.
ANKRD13A also known as Ankyrin Repeat Domain 13A is a protein weighing approximately 114 kDa. It contains ankyrin repeat motifs that facilitate protein-protein interactions making it important for cellular processes. ANKRD13A expresses widely across tissues with the highest levels in the brain heart and skeletal muscle. These repeat motifs are characteristic of proteins that participate in a variety of cellular functions suggesting ANKRD13A's role in maintaining cellular architecture and signaling.
Biological function summary
ANKRD13A interacts with several proteins implicating it in cellular adhesion and signaling pathways. It forms part of a complex involved in endocytosis and intracellular trafficking. These processes are essential for maintaining cellular communication and signaling balance. ANKRD13A's protein interactions suggest functions in regulating cell membrane dynamics and vesicle transport which are critical for constant cellular adaptation to environmental signals.
Pathways
ANKRD13A plays a significant role in endocytosis and neurotransmitter trafficking. It interacts within the endocytic pathway to regulate the internalization and sorting of membrane proteins. ANKRD13A has connections to clathrin-mediated endocytosis and may influence synaptic vesicle recycling. The protein associates with clathrin and adaptor protein complexes indicating its contribution to maintaining neurotransmitter homeostasis in neural pathways.
ANKRD13A has associations with neurological and cardiovascular conditions. Deregulation or mutations in ANKRD13A may contribute to neurodegenerative diseases such as Alzheimer's and heart diseases. The protein's link to dynamin and other cytoskeletal proteins is critical since these proteins play roles in amyloid precursor protein (APP) processing and endocytic pathways related to these illnesses. Understanding how ANKRD13A interacts in these contexts can help in exploring therapeutic options for these conditions.
