产品简要
公司名称 :
MyBioSource
产品类型 :
抗体
产品名称 :
山羊多克隆抗人类NALP3/NLRP3
目录 :
MBS241660
规格 :
0.05毫克
价格 :
495美元
克隆性 :
多克隆
宿主 :
山羊
共轭标签 :
未共轭
反应物种 :
人类
应用 :
酶联免疫吸附测定, 免疫组化, 酶免疫法
更多信息或购买 :
产品信息
目录号 :
MBS241660
产品类型 :
抗体
产品全称 :
山羊多克隆抗人类NALP3/NLRP3
产品简称 :
NALP3/NLRP3
产品名称同义词 :
Anti-NALP3 / NLRP3 Antibody (Internal) IHC-plus; NLRP3; AGTAVPRL; AII; C1orf7; Caterpiller protein 1.1; Cryopyrin; FCAS; FCU; PYPAF1; NALP3; CIAS1; CLR1.1; MWS; Human NALP3; NLRP3
其他名称 :
NACHT, LRR and PYD domains-containing protein 3 isoform a; NACHT, LRR and PYD domains-containing protein 3; NACHT, LRR and PYD domains-containing protein 3; cryopyrin; caterpiller protein 1.1; PYRIN-containing APAF1-like protein 1; NACHT, LRR and PYD containing protein 3; cold autoinflammatory syndrome 1 protein; NACHT domain-, leucine-rich repeat-, and PYD-containing protein 3; nucleotide-binding oligomerization domain, leucine rich repeat and pyrin domain containing 3; NLR family, pyrin domain containing 3; Angiotensin/vasopressin receptor AII/AVP-like; Caterpiller protein 1.1; CLR1.1; Cold autoinflammatory syndrome 1 protein; Cryopyrin; PYRIN-containing APAF1-like protein 1
产品基因名称 :
NALP3
产品基因名称同义词 :
NLRP3
其他基因名称 :
NLRP3;NLRP3;AII;AVP;FCU;MWS;FCAS;CIAS1;FCAS1;NALP3;C1orf7;CLR1.1;PYPAF1;AGTAVPRL;C1orf7;CIAS1;NALP3;PYPAF1;CLR1.1
UniProt数据库进入名 :
NALP3_HUMAN
克隆性 :
多克隆
宿主 :
山羊
反应物种 :
Gibbon, Gorilla, Human, Monkey. Predicted Reactivity: Bat, Pig (at least 90% immunogen sequence identity)
序列长度 :
1036
特异性 :
Human NLRP3. This antibody is expected to recognise all five reported isoforms (NP_004886.3; NP_899632.1; NP_001230062.1; NP_001120933.1; NP_001120934.1). Reported variants represent identical protein (NP_004886.3 and NP_001073289.1).
纯度 :
Immunoaffinity Purified
形式 :
三羟甲基氨基甲烷缓冲盐液, pH值7.3, 0.5% BSA, 0.02% 叠氮化钠
浓度 :
0.5毫克/毫升
储存稳定性 :
Store at -20 degree C. Minimize freezing and thawing.
检测过的应用 :
免疫组化(免疫组化-石蜡), 酶联免疫吸附测定(EIA)
应用笔记 :
ELISA (1:64000), IHC-P (2.5 ug/ml). Usage: Immunohistochemistry: was validated for use in immunohistochemistry on a panel of 21 formalin-fixed, paraffin-embedded (FFPE) human tissues after heat induced antigen retrieval in pH 6.0 citrate buffer. After incubation with the primary anti.
其它信息1 :
Target Species: Human. Immunogen Description: Synthetic peptide C-DLYEKAKRDEPK from an internal region of human NLRP3 (NP_004886.3; NP_899632.1; NP_001230062.1; NP_001120933.1; NP_001120934.1). Percent identity by BLAST analysis: Human, Gorilla, Gibbon, Monkey, Marmoset (100%).
其他信息2 :
Immunogen Type: Synthetic peptide. Immunogen: NALP3 / NLRP3 antibody was raised against synthetic peptide C-DLYEKAKRDEPK from an internal region of human NLRP3 (NP_004886.3; NP_899632.1; NP_001230062.1; NP_001120933.1; NP_001120934.1). Percent identity by BLAST analysis: Human, Gorilla, Gibbon, Monkey, Marmoset (100%); Bat, Panda, Pig (92%); Dog, Bovine, Rabbit (83%). Antigen Modification: Internal
产品描述 :
This gene encodes a pyrin-like protein containing a pyrin domain, a nucleotide-binding site (NBS) domain, and a leucine-rich repeat (LRR) motif. This protein interacts with the apoptosis-associated speck-like protein PYCARD/ASC, which contains a caspase recruitment domain, and is a member of the NALP3 inflammasome complex. This complex functions as an upstream activator of NF-kappaB signaling, and it plays a role in the regulation of inflammation, the immune response, and apoptosis.
NCBI GI登录号 :
34878693
NCBI登录号 :
NP_004886.3
NCBI基因登录号 :
NM_004895.4
UniProt数据库登录号 :
Q96P20
NCBI分子量 :
115,968 Da
NCBI信号通路 :
Immune System Pathway (106386); Inflammasomes Pathway (366166); Influenza A Pathway (217173); Influenza A Pathway (217150); Innate Immune System Pathway (106387); NOD Pathway (198792); NOD-like Receptor Signaling Pathway (122191); NOD-like Receptor Signaling Pathway (122131); Nucleotide-binding Domain, Leucine Rich Repeat Containing Receptor (NLR) Signaling Pathways (366164); Pertussis Pathway (218111)
NCBI总结 :
This gene encodes a pyrin-like protein containing a pyrin domain, a nucleotide-binding site (NBS) domain, and a leucine-rich repeat (LRR) motif. This protein interacts with the apoptosis-associated speck-like protein PYCARD/ASC, which contains a caspase recruitment domain, and is a member of the NALP3 inflammasome complex. This complex functions as an upstream activator of NF-kappaB signaling, and it plays a role in the regulation of inflammation, the immune response, and apoptosis. Mutations in this gene are associated with familial cold autoinflammatory syndrome (FCAS), Muckle-Wells syndrome (MWS), chronic infantile neurological cutaneous and articular (CINCA) syndrome, and neonatal-onset multisystem inflammatory disease (NOMID). Multiple alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. Alternative 5' UTR structures are suggested by available data; however, insufficient evidence is available to determine if all of the represented 5' UTR splice patterns are biologically valid. [provided by RefSeq, Oct 2008]
UniProt数据库总结 :
NLRP3: May function as an inducer of apoptosis. Interacts selectively with ASC and this complex may function as an upstream activator of NF-kappa-B signaling. Inhibits TNF-alpha induced activation and nuclear translocation of RELA/NF-KB p65. Also inhibits transcriptional activity of RELA. Activates caspase-1 in response to a number of triggers including bacterial or viral infection which leads to processing and release of IL1B and IL18. Defects in NLRP3 are the cause of familial cold autoinflammatory syndrome type 1 (FCAS1); also known as familial cold urticaria. FCAS are rare autosomal dominant systemic inflammatory diseases characterized by episodes of rash, arthralgia, fever and conjunctivitis after generalized exposure to cold. Defects in NLRP3 are a cause of Muckle-Wells syndrome (MWS); also known as urticaria-deafness-amyloidosis syndrome. MWS is a hereditary periodic fever syndrome characterized by fever, chronic recurrent urticaria, arthralgias, progressive sensorineural deafness, and reactive renal amyloidosis. The disease may be severe if generalized amyloidosis occurs. Defects in NLRP3 are the cause of chronic infantile neurologic cutaneous and articular syndrome (CINCA); also known as neonatal onset multisystem inflammatory disease (NOMID). CINCA is a rare congenital inflammatory disorder characterized by a triad of neonatal onset of cutaneous symptoms, chronic meningitis and joint manifestations with recurrent fever and inflammation. Belongs to the NLRP family. 5 isoforms of the human protein are produced by alternative splicing. Protein type: Inhibitor. Chromosomal Location of Human Ortholog: 1q44. Cellular Component: cytoplasm; cytosol. Molecular Function: peptidoglycan binding; protein binding; ATP binding. Biological Process: caspase activation; apoptosis; negative regulation of acute inflammatory response; interleukin-1 beta production; positive regulation of caspase activity; defense response; positive regulation of interleukin-1 beta secretion; negative regulation of NF-kappaB import into nucleus; signal transduction; protein oligomerization; activation of NF-kappaB transcription factor; negative regulation of interleukin-1 beta secretion; inhibition of NF-kappaB transcription factor; negative regulation of inflammatory response; innate immune response; interleukin-18 production; interleukin-1 secretion; detection of biotic stimulus; inflammatory response; defense response to virus. Disease: Cinca Syndrome; Familial Cold Autoinflammatory Syndrome 1; Muckle-wells Syndrome
尺寸1 :
0.05毫克
价格1 :
495美元
更多信息或购买 :
公司信息
MyBioSource
P.O. Box 153308
San Diego, CA 92195-3308
sales@mybiosource.com
https://www.mybiosource.com
1-858-633-0165
公司总部: 美国
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