激情深爱五月-激情视频亚洲-激情视频综合网-激情四房-激情婷婷-激情婷婷丁香

最近搜索:細胞培養 微生物學 分子生物 生物化學
首頁>>免疫學>>一抗>>細胞凋亡誘導蛋白NALP3抗體
細胞凋亡誘導蛋白NALP3抗體
  • 產品貨號:
    BN41607R
  • 中文名稱:
    細胞凋亡誘導蛋白NALP3抗體
  • 英文名稱:
    Rabbit anti-NALP3/CIAS1 Polyclonal antibody
  • 品牌:
    Biorigin
  • 貨號

    產品規格

    售價

    備注

  • BN41607R-50ul

    50ul

    ¥1486.00

    交叉反應:Human,Mouse,Rat,Dog 推薦應用:WB,IHC-P,IHC-F,IF,Flow-Cyt,ELISA

  • BN41607R-100ul

    100ul

    ¥2360.00

    交叉反應:Human,Mouse,Rat,Dog 推薦應用:WB,IHC-P,IHC-F,IF,Flow-Cyt,ELISA

  • BN41607R-200ul

    200ul

    ¥3490.00

    交叉反應:Human,Mouse,Rat,Dog 推薦應用:WB,IHC-P,IHC-F,IF,Flow-Cyt,ELISA

產品描述

英文名稱NALP3/CIAS1
中文名稱細胞凋亡誘導蛋白NALP3抗體
別    名LRR and PYD domains-containing protein 3; AGTAVPRL; AII/AVP antibody Angiotensin/vasopressin receptor AII/AVP like; Angiotensin/vasopressin receptor AII/AVP-like; C1orf7; Caterpiller protein 1.1; CIAS 1; CIAS1; CLR1.1; Cold autoinflammatory syndrome 1; Cold autoinflammatory syndrome 1 protein; Cryopyrin; Familial cold autoinflammatory syndrome; FCAS; FCU; Muckle-Wells syndrome; MWS; NACHT; NACHT LRR and PYD containing protein 3; NALP 3; NALP3; NALP3_HUMAN; NLRP3; PYPAF 1; PYPAF1 antibody PYRIN containing APAF1 like protein 1; PYRIN-containing APAF1-like protein 1.  





研究領域腫瘤  心血管  細胞生物  免疫學  信號轉導  細胞凋亡  轉錄調節因子  
抗體來源Rabbit
克隆類型Polyclonal
交叉反應Human, Mouse, Rat, Dog, 
產品應用WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 Flow-Cyt=2ug/Test ICC=1:100-500 IF=1:200-800 (石蠟切片需做抗原修復)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量114kDa
細胞定位細胞核 細胞漿 分泌型蛋白 
性    狀Liquid
濃    度1mg/ml
免 疫 原KLH conjugated synthetic peptide derived from human Cryopyrin:15-120/1036 
亞    型IgG
純化方法affinity purified by Protein A
儲 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
PubMedPubMed
產品介紹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.

Function:
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.

Subcellular Location:
Cytoplasm.

Tissue Specificity:
Expressed in blood leukocytes. Strongly expressed in polymorphonuclear cells and osteoblasts. Undetectable or expressed at a lower magnitude in B- and T-lymphoblasts, respectively. High level of expression detected in chondrocytes. Detected in non-keratinizing epithelia of oropharynx, esophagus and ectocervix and in the urothelial layer of the bladder.

DISEASE:
Defects in NLRP3 are the cause of familial cold autoinflammatory syndrome type 1 (FCAS1) [MIM:120100]; 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) [MIM:191900]; 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) [MIM:607115]; 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.

Similarity:
Belongs to the NLRP family.
Contains 1 DAPIN domain.
Contains 9 LRR (leucine-rich) repeats.
Contains 1 NACHT domain.

SWISS:
Q96P20

Gene ID:
114548

Database links:

Entrez Gene: 114548 Human

Entrez Gene: 216799 Mouse

Entrez Gene: 287362 Rat

Omim: 606416 Human

SwissProt: Q96P20 Human

SwissProt: Q8R4B8 Mouse

Unigene: 159483 Human

Unigene: 54174 Mouse




Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.


主站蜘蛛池模板: 亚洲国产精品一区二区手机 | 久久久无码精品亚洲日韩91 | 久久久久99精品成人免费 | 亚洲天天在线日亚洲洲精 | 国产毛片a | 国产a级毛片久久精品电影 国产a级毛片久久久精品毛片 | 欧美另类精品xxxx孕妇 | 久久91精品国产91久久综合 | 日木特级黄色a大片 | 日本又黄又爽又色又刺激的视频 | 国产日b视频 | 国产精品午夜一级毛片密呀 | 国精产品一二三区传媒公司 | 国产成人精品日本亚洲第一区 | 91精品视频在线播放 | 麻豆app官网入口 | 久久天天丁香婷婷中文字幕 | 国产欧美动漫日韩在线一区二区三 | 精东天美麻豆果冻传媒性巴克:人气高的可截屏姐妹直播 | 一区二区三区在线播放 | 天天干在线色视频 日日夜夜操天天操 | 国产乱伦精品一区二区三区久久 | 波多野结衣视频在线观看 | 日本欧美一区二区三区四区 | 久久久av波多野一区二区 | 91久久精品国产91久久公 | 99精品欧美一区二区蜜桃免费 | 久久受www免费人成_看片中文 | 国产精品日韩欧美一区二区视频 | 91久久精品一区二区 | 精品亚洲一区二区三区在线播放 | 奇米精品一区二区三区 | 欧美日韩一二 | wbg国产乱码卡一卡二卡三新区又有新动作 | 99久久国产综合精品成人影 | 岛国精品一区免费视频 | 久久精品欧美曰韩精品 | 麻豆自制传媒最新网站 | 精品久久久国产中文字幕 | 日韩一区国产二区欧美三区 | 国产午夜精品一区二区不卡 |