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SAMD9L Knockout Cell Lines

Gene: SAMD9L

Official Full Name: sterile alpha motif domain containing 9 likeprovided by HGNC

Gene Summary: This gene encodes a cytoplasmic protein that acts as a tumor suppressor but also plays a key role in cell proliferation and the innate immune response to viral infection. The encoded protein contains an N-terminal sterile alpha motif domain. Naturally occurring mutations in this gene are associated with myeloid disorders such as juvenile myelomonocytic leukemia, acute myeloid leukemia, and myelodysplastic syndrome. Naturally occurring mutations are also associated with hepatitis-B related hepatocellular carcinoma, normophosphatemic familial tumoral calcinosis, and ataxia-pancytopenia syndrome. [provided by RefSeq, Apr 2017]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
GP00537 SAMD9L gRNA1-gRNA2 KO plasmid SAMD9L $850
GP00626 SAMD9L gRNA1-gRNA2 KO plasmid SAMD9L $850
KO00806 SAMD9L Knockout cell line(U-87 MG) Human SAMD9L 1:3~1:4 Negative Online Inquiry
KO14368 SAMD9L Knockout cell line (A549) Human SAMD9L 1:3~1:4 Negative Online Inquiry

Background

SAMD9L gene knockout cell lines are genetically engineered cellular models that have had the SAMD9L gene disrupted or inactivated, enabling researchers to investigate the functional role of this gene in various biological contexts. SAMD9L, or sterile alpha motif domain-containing protein 9-like, is implicated in cell growth, differentiation, and immune responses. By utilizing knockout cell lines, scientists can elucidate the gene's contributions to these processes and better understand its involvement in pathological conditions, such as cancer and autoimmune diseases.

The mechanism of action of SAMD9L gene knockout cell lines primarily revolves around the absence of the SAMD9L protein, which serves as a critical regulator in several signaling pathways. Without the expression of SAMD9L, alterations in cellular behavior—such as rapid proliferation, changes in apoptosis rates, and modulation of immune responses—can be observed. Researchers leverage these alterations to investigate the protein's role in cellular homeostasis and disease progression.

The scientific significance of SAMD9L gene knockout cell lines extends to both basic research and clinical applications. In academic laboratories, these cell lines are invaluable for exploring the biochemical pathways in which SAMD9L is involved, thereby advancing the understanding of disease mechanisms. In clinical settings, insights gained from these studies could contribute to novel therapeutic strategies targeting conditions linked to SAMD9L dysregulation.

Compared to alternative models, such as overexpression systems or wild-type cell lines, SAMD9L gene knockout cell lines provide a more precise and representative study of gene function by removing the confounding effects of the gene’s activity. These knockout models enable the evaluation of phenotypic consequences and therapeutic targets with greater accuracy.

For researchers and clinicians focused on the implications of SAMD9L in health and disease, these knockout cell lines represent a critical tool. Their application can deepen insights into autoimmune disorders and cancer biology, positioning users at the forefront of significant research breakthroughs.

At [Your Company Name], we specialize in the development and provision of high-quality biological products that empower researchers to push the boundaries of understanding in genetics and molecular biology. Our SAMD9L gene knockout cell lines are rigorously validated, ensuring reliability and reproducibility that our customers can trust.

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

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