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NOD1 Knockout Cell Lines

Gene: NOD1

Official Full Name: nucleotide binding oligomerization domain containing 1provided by HGNC

Gene Summary: This gene encodes a member of the nucleotide-binding oligomerization domain (NOD)-like receptor (NLR) family of proteins. The encoded protein plays a role in innate immunity by acting as a pattern-recognition receptor (PRR) that binds bacterial peptidoglycans and initiates inflammation. This protein has also been implicated in the immune response to viral and parasitic infection. Major structural features of this protein include an N-terminal caspase recruitment domain (CARD), a centrally located nucleotide-binding domain (NBD), and 10 tandem leucine-rich repeats (LRRs) in its C terminus. The CARD is involved in apoptotic signaling, LRRs participate in protein-protein interactions, and mutations in the NBD may affect the process of oligomerization and subsequent function of the LRR domain. Mutations in this gene are associated with asthma, inflammatory bowel disease, Behcet disease and sarcoidosis in human patients. [provided by RefSeq, Aug 2017]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO09527 NOD1 Knockout cell line (HeLa) Human NOD1 1:3~1:6 Negative Online Inquiry
KO09528 NOD1 Knockout cell line (HCT 116) Human NOD1 1:2~1:4 Negative Online Inquiry
KO09529 NOD1 Knockout cell line (HEK293) Human NOD1 1:3~1:6 Negative Online Inquiry
KO09530 NOD1 Knockout cell line (A549) Human NOD1 1:3~1:4 Negative Online Inquiry

Background

NOD1 Gene Knockout Cell Lines are specialized cell cultures that have undergone genetic modification to disrupt the NOD1 gene, a critical component of the innate immune response. The NOD1 (Nucleotide-binding oligomerization domain-containing protein 1) plays a vital role in recognizing specific bacterial peptidoglycan fragments, thereby initiating downstream signaling pathways that activate immune defense mechanisms. By utilizing these knockout cell lines, researchers can investigate the function of NOD1 in immune signaling cascades, as well as its implications in inflammation, infection, and autoimmune diseases.

The primary mechanism behind the functionality of NOD1 involves the detection of pathogen-associated molecular patterns (PAMPs) and the subsequent activation of pro-inflammatory pathways through nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) and mitogen-activated protein kinases (MAPKs). The NOD1 Gene Knockout Cell Lines provide a unique model to delineate these pathways by allowing scientists to study the physiological and biochemical responses in the absence of NOD1, helping to elucidate its role in various pathological conditions.

In terms of scientific importance, these cell lines are invaluable in research settings focused on understanding immunological responses, developing novel therapeutic strategies, and conducting drug discovery. They serve as a model system for screening potential anti-inflammatory drugs and studying the effects of different stimuli on gene expression related to immune responses.

What sets our NOD1 Gene Knockout Cell Lines apart from alternative products is their high-quality genetic modification, ensuring a consistent and reliable loss of function. This specificity allows for more accurate modeling of diseases related to NOD1 dysregulation, giving researchers confidence in their experimental findings.

For researchers and clinicians focused on immunology and inflammation, these knockout cell lines provide an essential tool for advancing our understanding and treatment of various diseases. By leveraging our NOD1 Gene Knockout Cell Lines, stakeholders can streamline their research efforts, promote reproducibility, and accelerate discoveries in immune therapeutics.

As a leader in biological products, our company is dedicated to providing researchers with high-quality, precision-modified cell lines and ongoing support, ensuring they have the tools required to explore and innovate in the realm of immune research.

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

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