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AP1G2 Knockout Cell Lines

Gene: AP1G2

Official Full Name: adaptor related protein complex 1 subunit gamma 2provided by HGNC

Gene Summary: Adaptins are important components of clathrin-coated vesicles transporting ligand-receptor complexes from the plasma membrane or from the trans-Golgi network to lysosomes. The adaptin family of proteins is composed of four classes of molecules named alpha, beta-, beta prime- and gamma- adaptins. Adaptins, together with medium and small subunits, form a heterotetrameric complex called an adaptor, whose role is to promote the formation of clathrin-coated pits and vesicles. The protein encoded by this gene is a gamma-adaptin protein and it belongs to the adaptor complexes large subunits family. This protein along with the complex is thought to function at some trafficking step in the complex pathways between the trans-Golgi network and the cell surface. [provided by RefSeq, Aug 2017]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO33755 AP1G2 Knockout cell line (HeLa) Human AP1G2 1:3~1:6 Negative Online Inquiry
KO33756 AP1G2 Knockout cell line (HCT 116) Human AP1G2 1:2~1:4 Negative Online Inquiry
KO33757 AP1G2 Knockout cell line (HEK293) Human AP1G2 1:3~1:6 Negative Online Inquiry
KO33758 AP1G2 Knockout cell line (A549) Human AP1G2 1:3~1:4 Negative Online Inquiry

Background

AP1G2 Gene Knockout Cell Lines are specifically engineered cellular models designed to study the functional consequences of the AP1G2 gene's absence. This gene plays a critical role in intracellular transport processes, particularly in the clathrin-mediated endocytosis pathway, which is essential for the uptake of various biomolecules and signaling receptors. By employing CRISPR/Cas9 technology, the production of these knockout cell lines ensures that the AP1G2 gene is effectively disrupted, providing researchers with a robust system to investigate the gene’s function and its broader implications in cellular homeostasis and disease mechanisms.

Key functions of the AP1G2 gene include facilitating the formation of clathrin-coated vesicles, thus regulating cargo sorting and trafficking within cells. The knockout of this gene creates an opportunity to understand how loss of AP1G2 affects cellular morphologies, receptor recycling, and signal transduction pathways. It also opens avenues for exploring how dysregulation of these processes contributes to a variety of diseases such as cancer, neurodegeneration, and metabolic disorders.

In research and clinical settings, AP1G2 Gene Knockout Cell Lines provide an important tool for the advancement of drug discovery and therapeutic development. By elucidating the role of AP1G2 in disease models, researchers can identify potential targets for intervention in therapeutic strategies, enhancing our understanding of pathophysiology.

What sets our AP1G2 Gene Knockout Cell Lines apart from alternatives is their comprehensive validation and characterizations, including rigorous QC assays that verify gene disruption and maintain cellular integrity. Our lines come with detailed documentation of their usage in relevant experimental conditions, empowering researchers to confidently apply them in their studies.

For researchers and clinicians seeking reliable models to investigate gene function and cellular mechanisms, our AP1G2 Gene Knockout Cell Lines stand out as an invaluable resource. They are instrumental in translating basic research findings into clinical applications, ultimately aiding in the development of innovative therapeutics.

At our company, we are committed to advancing biological research through expert development and provision of high-quality cell models. Our experience underscores a dedication to providing not only exceptional products but also the support necessary for researchers to drive their projects forward.

Please note that all services are for research use only. Not intended for any clinical use.

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