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PSPH Knockout Cell Lines

Gene: PSPH

Official Full Name: phosphoserine phosphataseprovided by HGNC

Gene Summary: The protein encoded by this gene belongs to a subfamily of the phosphotransferases. This encoded enzyme is responsible for the third and last step in L-serine formation. It catalyzes magnesium-dependent hydrolysis of L-phosphoserine and is also involved in an exchange reaction between L-serine and L-phosphoserine. Deficiency of this protein is thought to be linked to Williams syndrome. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO35839 PSPH Knockout cell line (HeLa) Human PSPH 1:3~1:6 Negative Online Inquiry
KO35840 PSPH Knockout cell line (HCT 116) Human PSPH 1:2~1:4 Negative Online Inquiry
KO35841 PSPH Knockout cell line (HEK293) Human PSPH 1:3~1:6 Negative Online Inquiry
KO35842 PSPH Knockout cell line (A549) Human PSPH 1:3~1:4 Negative Online Inquiry

Background

PSPH Gene Knockout Cell Lines are genetically modified cell lines designed to specifically disrupt the function of the phosphoserine phosphatase (PSPH) gene. This gene plays a critical role in the synthesis and regulation of amino acids, influencing numerous metabolic pathways. By employing CRISPR-Cas9 technology, these knockout cell lines allow researchers to efficiently investigate the biological role of PSPH and its involvement in various physiological processes and diseases, such as cancer and neurodegenerative disorders.

The primary mechanism by which these cell lines function is through the targeted deletion or disruption of the PSPH gene, leading to the elimination of its expression. This provides a unique model system to study the metabolic consequences of PSPH deficiency. The resultant changes in cell behavior and function can yield valuable insights into the physiological processes governed by PSPH, enabling researchers to elucidate its potential as a therapeutic target.

The scientific importance of PSPH Gene Knockout Cell Lines lies in their applicability in both fundamental research and translational studies. They serve as crucial tools for investigating the pathways involved in amino acid metabolism and can enhance our understanding of the molecular underpinnings of related diseases. In clinical settings, these models hold promise for testing novel therapeutic strategies that target PSPH-related pathways, thereby contributing to the development of innovative treatments.

Compared to traditional knockout models, such as those generated through homologous recombination, PSPH Gene Knockout Cell Lines offer several distinct advantages. They exhibit rapid generation times and reduced off-target effects due to the precise approach of CRISPR technology. Additionally, the standardized and validated nature of these cell lines ensures consistent results across experiments, contributing to reproducibility in scientific research.

For researchers and clinicians looking to deepen their understanding of amino acid metabolism and explore novel interventions targeting PSPH, our PSPH Gene Knockout Cell Lines represent an invaluable resource. Backed by our company’s extensive experience in the development of advanced biological products, we are committed to providing high-quality models that empower groundbreaking research and innovation in health sciences.

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

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