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SPTLC2 Knockout Cell Lines

Gene: SPTLC2

Official Full Name: serine palmitoyltransferase long chain base subunit 2provided by HGNC

Gene Summary: This gene encodes a long chain base subunit of serine palmitoyltransferase. Serine palmitoyltransferase, which consists of two different subunits, is the key enzyme in sphingolipid biosynthesis. It catalyzes the pyridoxal-5-prime-phosphate-dependent condensation of L-serine and palmitoyl-CoA to 3-oxosphinganine. Mutations in this gene were identified in patients with hereditary sensory neuropathy type I. [provided by RefSeq, Mar 2011]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO07683 SPTLC2 Knockout cell line (HeLa) Human SPTLC2 1:3~1:6 Negative Online Inquiry
KO07684 SPTLC2 Knockout cell line (HCT 116) Human SPTLC2 1:2~1:4 Negative Online Inquiry
KO07685 SPTLC2 Knockout cell line (HEK293) Human SPTLC2 1:3~1:6 Negative Online Inquiry
KO07686 SPTLC2 Knockout cell line (A549) Human SPTLC2 1:3~1:4 Negative Online Inquiry

Background

SPTLC2 Gene Knockout Cell Lines are specialized cellular models engineered to silence the SPTLC2 gene, a critical component in the biosynthesis of sphingolipids, which play essential roles in various cellular processes, including apoptosis, cell signaling, and membrane integrity. By utilizing CRISPR/Cas9 technology, these cell lines provide a robust platform for studying the implications of SPTLC2 deficiency on sphingolipid metabolism and related cellular functions.

The primary mechanism of action involves the precise deletion of the SPTLC2 gene, which leads to a significant alteration in the sphingolipid biosynthetic pathway. Researchers can explore the resulting biochemical and phenotypic changes, such as altered cell proliferation, increased oxidative stress responses, and potential changes in cell communication pathways. This allows for in-depth investigation into diseases linked to sphingolipid dysregulation, such as neurodegenerative diseases, cancer, and metabolic disorders.

The scientific importance of SPTLC2 Gene Knockout Cell Lines extends beyond basic research; they are invaluable tools for drug discovery and development. By providing insights into the pathological mechanisms driven by sphingolipid imbalances, these cell lines can guide therapeutic interventions and facilitate the identification of novel drug targets. Furthermore, their ability to mimic disease-specific conditions enhances their applicability in preclinical models for evaluating drug efficacy.

Compared to traditional models, these knockout cell lines offer unique advantages, including higher specificity in targeting gene function, the reproducibility of results, and the opportunity to create isogenic controls. This level of precision reduces experimental variability and enhances the reliability of research findings.

For researchers and clinicians investigating sphingolipid-related pathologies, the SPTLC2 Gene Knockout Cell Lines represent a crucial asset. Their design fosters groundbreaking discoveries in cellular biology, enabling the translation of scientific findings into tangible therapeutic strategies.

Our company specializes in the development and supply of high-quality biological reagents and models. With a commitment to innovation and excellence, we provide researchers with the tools necessary to advance their studies in cellular and molecular biology, ensuring accurate and reproducible results in their experiments.

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

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