Product Name
NLRP12, Polyclonal Antibody
Full Product Name
NLRP12, NT (NLRP12, NALP12, PYPAF7, RNO, NACHT, LRR and PYD domains-containing protein 12, Monarch-1, PYRIN-containing APAF1-like protein 7, Regulated by nitric oxide)
Product Synonym Names
Anti -NLRP12, NT (NLRP12, NALP12, PYPAF7, RNO, NACHT, LRR and PYD domains-containing protein 12, Monarch-1, PYRIN-containing APAF1-like protein 7, Regulated by nitric oxide)
Product Gene Name
anti-NLRP12 antibody
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Chromosome Location
Chromosome: 19; NC_000019.9 (54296838..54327657, complement). Location: 19q13.42
3D Structure
ModBase 3D Structure for P59046
Purity/Purification
Affinity Purified
Purified by Protein A affinity chromatography.
Form/Format
Supplied as a liquid in PBS, pH 7.2, 0.09% sodium azide.
Immunogen
NLRP12 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 182-212 amino acids from the N-terminal region of human NLRP12.
Preparation and Storage
May be stored at 4 degree C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20 degree C. Aliquots are stable for 12 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Other Notes
Small volumes of anti-NLRP12 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Related Product Information for
anti-NLRP12 antibody
This gene encodes a member of the CATERPILLER family of cytoplasmic proteins. The encoded protein, which contains an N-terminal pyrin domain, a NACHT domain, a NACHT-associated domain, and a C-terminus leucine-rich repeat region, functions as an attenuating factor of inflammation by suppressing inflammatory responses in activated monocytes. Alternatively spliced transcript variants encoding distinct isoforms have been described but the full-length nature of some of these has not been determined.
Product Categories/Family for anti-NLRP12 antibody
Antibodies; Abs to Nitric Oxide
Applications Tested/Suitable for anti-NLRP12 antibody
ELISA (EL/EIA), Western Blot (WB), Immunohistochemistry (IHC)
Application Notes for anti-NLRP12 antibody
Suitable for use in Western Blot, Immunohistochemistry, ELISA
Dilution: ELISA: 1:1,000
Western Blot: 1:100-500
Immunohistochemistry: 1:10-50
NCBI/Uniprot data below describe general gene information for NLRP12. It may not necessarily be applicable to this product.
NCBI Accession #
NP_653288.1
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NCBI GenBank Nucleotide #
NM_144687.3
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UniProt Primary Accession #
P59046
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UniProt Secondary Accession #
Q8NEU4; Q9BY26[Other Products]
UniProt Related Accession #
P59046[Other Products]
Molecular Weight
120,173 Da[Similar Products]
NCBI Official Full Name
NACHT, LRR and PYD domains-containing protein 12 isoform 2
NCBI Official Synonym Full Names
NLR family, pyrin domain containing 12
NCBI Official Symbol
NLRP12 [Similar Products]
NCBI Official Synonym Symbols
RNO; PAN6; RNO2; FCAS2; NALP12; PYPAF7; CLR19.3
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NCBI Protein Information
NACHT, LRR and PYD domains-containing protein 12; monarch 1; regulated by nitric oxide; PYRIN-containing APAF1-like protein 7; nucleotide-binding oligomerization domain, leucine rich repeat and pyrin domain containing 12
UniProt Protein Name
NACHT, LRR and PYD domains-containing protein 12
UniProt Synonym Protein Names
Monarch-1; PYRIN-containing APAF1-like protein 7; Regulated by nitric oxide
Protein Family
NACHT, LRR and PYD domains-containing protein
UniProt Gene Name
NLRP12 [Similar Products]
UniProt Synonym Gene Names
NALP12; PYPAF7; RNO [Similar Products]
UniProt Entry Name
NAL12_HUMAN
NCBI Summary for NLRP12
This gene encodes a member of the CATERPILLER family of cytoplasmic proteins. The encoded protein, which contains an N-terminal pyrin domain, a NACHT domain, a NACHT-associated domain, and a C-terminus leucine-rich repeat region, functions as an attenuating factor of inflammation by suppressing inflammatory responses in activated monocytes. Mutations in this gene cause familial cold autoinflammatory syndrome type 2. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2013]
UniProt Comments for NLRP12
NLRP12: May mediate activation of CASP1 via ASC and promote activation of NF-kappa-B via IKK. Defects in NLRP12 are the cause of familial cold autoinflammatory syndrome type 2 (FCAS2). FCAS are rare autosomal dominant systemic inflammatory diseases characterized by episodes of rash, arthralgia, fever and conjunctivitis after generalized exposure to cold. Belongs to the NLRP family. 5 isoforms of the human protein are produced by alternative splicing.
Chromosomal Location of Human Ortholog: 19q13.42
Cellular Component: cytoplasm; nucleus
Molecular Function: protein binding; caspase activator activity; ATP binding
Biological Process: caspase activation; release of cytoplasmic sequestered NF-kappaB; negative regulation of cytokine secretion; negative regulation of interleukin-6 biosynthetic process; positive regulation of interleukin-1 beta secretion; negative regulation of I-kappaB kinase/NF-kappaB cascade; regulation of caspase activity; signal transduction; negative regulation of signal transduction; negative regulation of Toll signaling pathway; inhibition of NF-kappaB transcription factor; negative regulation of inflammatory response; positive regulation of MHC class I biosynthetic process; negative regulation of protein amino acid autophosphorylation; regulation of I-kappaB kinase/NF-kappaB cascade; negative regulation of interleukin-1 secretion; regulation of interleukin-18 biosynthetic process; positive regulation of inflammatory response
Disease: Familial Cold Autoinflammatory Syndrome 2
Research Articles on NLRP12
1. Even with a variable range of associated manifestations, the extreme sensitivity to cold represents the main clinical hallmark in an individual carrying the p.D294E mutation of the NLRP12 gene.
Precautions
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