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PGAP2 Knockout Cell Lines

Gene: PGAP2

Official Full Name: post-GPI attachment to proteins 2provided by HGNC

Gene Summary: The protein encoded by this gene plays a role in the maturation of glycosylphosphatidylinositol (GPI) anchors on GPI-anchored proteins. Mutations in this gene are associated with an autosomal recessive syndrome characterized by hyperphosphatasia and intellectual disability. [provided by RefSeq, Jul 2017]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO27654 PGAP2 Knockout cell line (HeLa) Human PGAP2 1:3~1:6 Negative Online Inquiry
KO27655 PGAP2 Knockout cell line (HCT 116) Human PGAP2 1:2~1:4 Negative Online Inquiry
KO27656 PGAP2 Knockout cell line (HEK293) Human PGAP2 1:3~1:6 Negative Online Inquiry
KO27657 PGAP2 Knockout cell line (A549) Human PGAP2 1:3~1:4 Negative Online Inquiry

Background

PGAP2 Gene Knockout Cell Lines are specialized cellular models engineered to selectively inactivate the PGAP2 gene, which plays a crucial role in the glycosylation of proteins and the functioning of the immune system. These knockout cell lines utilize CRISPR/Cas9 technology for precise gene editing, allowing researchers to study the consequences of PGAP2 deficiency on cellular processes, protein modification pathways, and related signaling cascades effectively.

The key function of the PGAP2 knockout cell lines is to facilitate the exploration of protein glycosylation abnormalities, which can contribute to various diseases, including immunodeficiencies and cancers. By observing the cellular behavior in the absence of PGAP2, researchers can elucidate its physiological roles, thereby advancing our understanding of glycosylation-related disorders and potential therapeutic targets. In clinical settings, these cell lines can be vital in drug development processes, enabling the assessment of treatment efficacy in glycosylation-deficient cellular environments.

One significant advantage of our PGAP2 Gene Knockout Cell Lines over other alternatives lies in their robust validation and characterization data, ensuring the reliability and reproducibility of experimental results. Additionally, they are available in various background cell types, making them versatile tools tailored to various research needs.

For researchers and clinicians, the unique ability to manipulate the genetic landscape of these cell lines to mirror specific pathophysiological conditions represents substantial value, providing insights that can lead to breakthroughs in therapeutic strategies and personalized medicine.

Our company prides itself on a commitment to excellence in providing high-quality biological products. With a strong foundation in genetic engineering and dedication to advancing research, we equip scientists and healthcare professionals with the tools necessary to push the frontiers of science and improve patient outcomes.

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

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