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SPHK2 Knockout Cell Lines

Gene: SPHK2

Official Full Name: sphingosine kinase 2provided by HGNC

Gene Summary: This gene encodes one of two sphingosine kinase isozymes that catalyze the phosphorylation of sphingosine into sphingosine 1-phosphate. Sphingosine 1-phosphate mediates many cellular processes including migration, proliferation and apoptosis, and also plays a role in several types of cancer by promoting angiogenesis and tumorigenesis. The encoded protein may play a role in breast cancer proliferation and chemoresistance. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2011]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO08475 SPHK2 Knockout cell line (HeLa) Human SPHK2 1:3~1:6 Negative Online Inquiry
KO08476 SPHK2 Knockout cell line (HCT 116) Human SPHK2 1:2~1:4 Negative Online Inquiry
KO08477 SPHK2 Knockout cell line (HEK293) Human SPHK2 1:3~1:6 Negative Online Inquiry
KO08478 SPHK2 Knockout cell line (A549) Human SPHK2 1:3~1:4 Negative Online Inquiry

Background

SPHK2 Gene Knockout Cell Lines are engineered cellular models that have undergone targeted genetic modification to knock out the expression of the sphingosine kinase 2 (SPHK2) gene. This gene is crucial for sphingolipid metabolism, influencing various biological processes such as cell proliferation, apoptosis, and inflammatory responses. The absence of SPHK2 provides researchers with a powerful tool to elucidate the role of sphingosine kinase signaling pathways in health and disease.

These cell lines operate by utilizing CRISPR-Cas9 technology to create precise genetic alterations, ensuring a complete knockout of SPHK2 function. This genetic modification permits the study of phenotypic changes in cellular behavior, enabling researchers to dissect the underlying mechanisms of sphingosine signaling and its implications in pathologies ranging from cancer to neurodegenerative disorders.

The scientific importance of SPHK2 Gene Knockout Cell Lines lies in their application in both basic research and clinical settings. Researchers can gain insights into the role of SPHK2 in metabolic diseases, investigate potential therapeutic targets, and assess the efficacy of drug candidates that modulate sphingolipid signaling. Additionally, these models can enhance high-throughput screening and drug discovery processes, leading to novel treatment strategies.

Compared to alternative models, such as wild-type cell lines or less precise gene editing methods, SPHK2 Gene Knockout Cell Lines offer superior specificity and reliability. They eliminate background interference caused by residual SPHK2 expression, thus providing more robust and reproducible results. This specificity is vital for preclinical studies where accurate modeling of disease conditions is paramount.

For researchers and clinicians focusing on sphingolipid metabolism and its associated disease mechanisms, SPHK2 Gene Knockout Cell Lines represent a valuable asset. They not only enable detailed mechanistic studies but also contribute to the discovery of innovative therapeutic approaches in translational medicine.

Our company specializes in the development of advanced model systems and has a strong commitment to providing high-quality, reliable biological products. With a team of experienced scientists, we ensure that our products meet rigorous standards of scientific excellence and support the advancement of research in critical areas of human health.

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

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