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NOD1 encodes a member of the NOD (nucleotide-binding oligomerization domain) family. Additionally we are shipping NOD1 Antibodies (131) and NOD1 Kits (3) and many more products for this protein.
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findings illuminated a role for NOD1 signaling in attenuating H. pylori-induced Cdx2 (show CDX2 Proteins) expression in gastric epithelial cells
NOD1/CARD4 gene may influence the diagnosis and treatment of lung cancer
NOD1 and NOD2, two members of the NOD-like receptor family of pattern recognition receptors, are important mediators of ER-stress-induced inflammation in mouse and human cells
NOD1 signaling results in the induction of the cellular degradation pathway of autophagy and the development of pro-inflammatory responses that activate the adaptive immune system.
The higher NOD1 and NOD2 were observed in villi from patients who experienced recurrent spontaneous abortion compared with those who experienced a normal pregnancy.
Activation of the innate immune pathway via NOD1 may be partially responsible for the increased systemic inflammation and insulin (show INS Proteins) resistance in metabolic syndrome.
NOD1 rs2709800, NOD2 rs718226, rs2111235, rs7205423 and interaction between rs718226 and H. pylori infection may be related to risk of gastric lesions.
We found that RNA interference-induced Caspase-12 silencing increased NOD1, hBD1 (show DEFB1 Proteins) and hBD2 (show DEFB4 Proteins) expression
Human embryonic stem cell-derived endothelial cells are TLR4 (show TLR4 Proteins) deficient but respond to bacteria via NOD1.
A significant association of the NOD1 +32656 GG insertion variant with protection against infection with Chlamydia trachomatis has been detected [p: 0.0057; OR: 0.52].
The results indicate that Nod1 cooperates with Nod2 or TLRs to produce cytokines in macrophages in response to M. tuberculosis infection.
NOD1 and NOD2, play a collaborative role in T cell activation by alloantigen and that their blockade in vitro can inhibit T cell responses.
NOD1 activation induces cardiac dysfunction associated with excitation-contraction coupling impairment through NF-kappaB (show NFKB1 Proteins) activation.
Activation of NOD1 by DAP (show DAP Proteins) contributes to reperfusion injury via multiple signaling pathways.
Nod1 levels (and Nod2) in osteoclastogenesis are influenced by MyD88 (show MYD88 Proteins) signaling.
Data show that NOD1 or NOD2 synergizes with TLR4 (show TLR4 Proteins) in exacerbating the immune, sickness and brain responses to immune stimulation. Interactions of NLRs and TLRs at the immune cell level extend to interactions affecting brain function and behavior.
NOD1 and TLR4 (show TLR4 Proteins) signaling act synergistically to mobilize hematopoietic stem cells during bacterial infection.
Bacterial peptidoglycan stimulates adipocyte lipolysis via NOD1.
This gene encodes a member of the NOD (nucleotide-binding oligomerization domain) family. This member is a cytosolic protein. It contains 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. This protein is an intracellular pattern-recognition receptor (PRR) that initiates inflammation in response to a subset of bacteria through the detection of bacterial diaminopimelic acid. Multiple alternatively spliced transcript variants differring in the 5' UTR have been described, but the full-length nature of these variants has not been determined.
NLR family, CARD domain containing 1
, caspase recruitment domain family, member 4
, caspase recruitment domain-containing protein 4
, nucleotide-binding oligomerization domain, leucine rich repeat and CARD domain containing 1
, nucleotide-binding oligomerization domain-containing protein 1
, caspase recruitment domain 4