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- Table of Contents
Facts about NLR family CARD domain-containing protein 4.
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Human | |
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Gene Name: | NLRC4 |
Uniprot: | Q9NPP4 |
Entrez: | 58484 |
Belongs to: |
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No superfamily |
CARD12leucine rich repeat and CARD domaincontaining 4; caspase recruitment domain family, member 12; Caspase recruitment domain-containing protein 12; Clan protein; CLAN1ipaf; CLANCARD, LRR, and NACHT-containing protein; CLR2.1; Ice protease-activating factor; Ipaf; NLR family, CARD domain containing 4
Mass (kDA):
116.159 kDA
Human | |
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Location: | 2p22.3 |
Sequence: | 2; NC_000002.12 (32224449..32265743, complement) |
Isoform 2 is expressed ubiquitously, although highly expressed in lung and spleen. Isoform 1 is highly expressed in lung, followed by leukocytes especially monocytes, lymph node, colon, brain, prostate, placenta, spleen, bone marrow and fetal liver. Isoform 4 is only detected in brain.
Cytoplasm. Cytoplasm, cytosol. Cytoplasmic filaments.
The NLRC4 Marker is a peptide that targets cancer and is a boster product. This peptide could be used to kill and detect cancer cells as the primary antibody. Boster Bio has been providing high affinity primary antibodies as well as chemicals for cancer research for more than 10 years. Learn more about the NLRC4 Marker and its applications.
The BACE inhibitor NRLC4 has recently been found to block the activity of CD8 T cells. which is a molecule found on the T cell's surface and is a critical component of the T cells subset. T cells comprise about 20-30% of the lymphocytes in the peripheral blood. CD8 antigen is present on 80% of thymocytes, natural killer cells, and bone marrow cells. Boster Bio provides high-affinity primary antibodies against this marker that can aid in your research.
The NLRC4 Marker is a distinct molecule that's presence and activity can identify or target a particular type of cancer. Its unique cell-penetrating capabilities make it a suitable delivery system for chemotherapy. This research provides important new insights into the field of cancer immunotherapy. The peptide may also be beneficial in the development of more effective chemotherapy drugs.
The NLRC4 Inflammasome comprises of three parts including NLRC4, a receptor as well as the sensor ASC and the adaptor. ASC is recruited into the inflammasome in the aftermath of infection by S. typhimurium. Casparase-1 also gets recruited by this infection. Inflammasomes can be seen in the cytoplasm, and they are dissolvable. ASC is a soluble constituent that forms a massive paranuclear-speck with a diameter of around 1mm.
NLRC4 Acetylation has been identified in HEK293T cells that were transfected with Flag-tagged NLRC4 proteins. The mass spectrometer was utilized to examine the immunoprecipitates. The sequences of NLRC4 in seven species were aligned and the acetylated residues (K71 K272, K674 and K763) were highlighted in red.
The role of the NLRC4 marker in bacterial enteric inflammation has been extensively studied. It is vital for the removal and function bacteria. NLRC4 is expressed at basal levels in epithelial and immune cells. The expression of this marker is controlled by phosphorylation, ligand binding, and is regulated by the process of phosphorylation. This article will discuss some of the applications of this marker. We conclude that NLRC4 can be used to study the immune system's innate components.
NLRC4 is part of the AAA+ ATPase family. It has structural features common to other NLR proteins. It has a central NTPase domain, as well as two helical domains NLRR or LRR. The NLRC4 marker's C-terminal amino acid 440 is composed of 15 repeating structural units. Each unit is comprised of a beta strand that is leucine-rich and joined to an alpha helix that is short and short.
Inflammasomes are one of the major causes of inflammation in human diseases. Inflammasomes possess a variety of distinct structural and functional properties and are involved in a wide range of inflammation-related diseases. NLRC4 is a part of the inflammasome. It is responsible for the cleavage of a variety substrates, including the cytosolic flagellin. It triggers a variety of autoinflammatory processes that cause cell death. Gain-of function mutations are found near the ADP binding site of the NLRC4 gene, and are associated with skin rash, enterolitis, and chronically high levels of IL-18.
There are a variety of clinical applications for the NLRC4 marker. The protein is linked to the inflammasome, and co-localizes well with NLRP3 genes. NLRC4 is also co-localized with NLRP3 in vivo. However, the super-resolution microscope used in these experiments does not provide enough resolution to discern specific protein-protein interactions. IL-18 and NLRC4 also interact with each other.
This research could have implications for a range of diseases like type 2 diabetes and systemic Lupus. These findings could also prove beneficial to other areas of medicine. These studies are just the beginning. It is vital that we continue studying this complicated marker to better understand how the disease is developing. A person could develop a treatment for this disease when NLRC4 isn't functioning correctly.
The variants of NLRC4's gene were selected from the most current literature in accordance with their minor-allele frequency. The Asian population must have the minor allele frequency higher than 0.05. Furthermore, the selected SNPs were not located in the same region of linkage. The markers of NLRC4 were genotyped using MassARRAY and PCR primers designed by Agena Bioscience. Table 1 shows the sequences of the primers.
PMID: 11374873 by Geddes B.J., et al. Human CARD12 is a novel CED4/Apaf-1 family member that induces apoptosis.
PMID: 11472070 by Damiano J.S., et al. CLAN, a novel human CED-4-like gene.