国产免费看JIZZ视频_国产综合图片区_久久久国产精品韩国AV无码_色影天堂精品久久久久_欧美成人一区在线视频_国产精品小视频在线观看_亚洲日本半精品久久久久_2019无码中文字幕亚洲_亚洲69堂_欧美精品区

聯系電話

18321282235

產品展示/ PRODUCTS PLAY

我的位置:首頁  >  產品展示  >  抗體  >  單抗  >  Anti-alpha 1 Antitrypsin抗體

產品分類 / PRODUCT

Anti-alpha 1 Antitrypsin抗體
描述:

Anti-alpha 1 Antitrypsin抗體缺乏是Z常見的遺傳代謝病,能引起肺和肝的損傷。α1抗*為呼吸系統的非特異性可溶因子,與呼吸道抵抗力關系密切,它可抑制多種酶的活性,包括細菌的酶,以及中性白細胞溶酶體分泌的蛋白酶、彈性蛋白酶、膠原酶、纖維蛋白溶酶和*。

  • 產品型號:
  • 廠商性質:生產廠家
  • 更新時間:2015-10-21
  • 訪問量:123
產品介紹/ PRODUCT PRESENTATION

產品編號 yb-0096R
英文名稱 Anti-alpha 1 Antitrypsin抗體
中文名稱 α-1抗*抗體
別    名 A1-Antitrypsin; Tryptase; Alpha-1-Antitrypsin; alpha 1 Antitrypsin; A1A; A1AT; AAT; Alpha 1 antiproteinase; Alpha 1 antitrypsin; Alpha 1 protease inhibitor; alpha-1-AT; alpha1 PI; alpha1 proteinase inhibitor; Clade A (alpha 1 antiproteinase antitrypsin) member 1; MGC23330; MGC9222; PI; PI; PRO2275; Protease inhibitor 1 (anti elastase); Serpin A1; Serpin peptidase inhibitor clade A (alpha 1 antiproteinase antitrypsin) member 1; SerpinA1; A1AT_HUMAN; Alpha-1-antitrypsin; Alpha-1 protease inhibitor; Alpha-1-antiproteinase; Serpin A1.
Anti-alpha 1 Antitrypsin抗體 
說 明 書 0.1ml  0.2ml  
研究領域 心血管  免疫學  新陳代謝  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human, Mouse, Rat, Dog, Pig, Cow, 
產品應用 WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 (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 44kDa
細胞定位 細胞外基質 分泌型蛋白 
性    狀 Lyophilized or Liquid
濃    度 1mg/1ml
免 疫 原 KLH conjugated synthetic peptide derived from human alpha 1 Antitrypsin
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 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.

PubMed PubMed
產品介紹 background:
Alpha-1-antitrypsin is a protease inhibitor, deficiency of which is associated with emphysema and liver disease. The protein is encoded by a gene (PI) located on the distal long arm of chromosome 14.

Function:
Inhibitor of serine proteases. Its primary target is elastase, but it also has a moderate affinity for plasmin and thrombin. Irreversibly inhibits trypsin, chymotrypsin and plasminogen activator. The aberrant form inhibits insulin-induced NO synthesis in plaets, decreases coagulation time and has proteolytic activity against insulin and plasmin. 
Short peptide from AAT (SPAAT) is a reversible chymotrypsin inhibitor. It also inhibits elastase, but not trypsin. Its major physiological function is the protection of the lower respiratory tract against proteolytic destruction by human leukocyte elastase (HLE).

Subcellular Location:
Secreted.
Short peptide from AAT: Secreted, extracellular space, extracellular matrix. 

Tissue Specificity:
Plasma.

Post-translational modifications:
N-glycosylated. Differential glycosylation produces a number of isoforms. N-linked glycan at Asn-107 is alternatively di-antennary, tri-antennary or tetra-antennary. The glycan at Asn-70 is di-antennary with trace amounts of tri-antennary. Glycan at Asn-271 is exclusively di-antennary. Structure of glycans at Asn-70 and Asn-271 is Hex5HexNAc4. The structure of the antennae is Neu5Ac(alpha1-6)Gal(beta1-4)GlcNAc attached to the core structure Man(alpha1-6)[Man(alpha1-3)]Man(beta1-4)GlcNAc(beta1-4)GlcNAc. Some antennae are fucosylated, which forms a Lewis-X determinant. 
Proteolytic processing may yield the truncated form that ranges from Asp-30 to Lys-418. 

DISEASE:
Defects in SERPINA1 are the cause of alpha-1-antitrypsin deficiency (A1ATD) [MIM:613490]. A disorder whose most common manifestation is emphysema, which becomes evident by the third to fourth decade. A less common manifestation of the deficiency is liver disease, which occurs in children and adults, and may result in cirrhosis and liver failure. Environmental factors, particularly cigarette smoking, greatly increase the risk of emphysema at an earlier age.
缺乏是zui常見的遺傳代謝病,能引起肺和肝的損傷。α1抗*為呼吸系統的非特異性可溶因子,與呼吸道抵抗力關系密切,它可抑制多種酶的活性,包括細菌的酶,以及中性白細胞溶酶體分泌的蛋白酶、彈性蛋白酶、膠原酶、纖維蛋白溶酶和*。α1抗*的缺乏與慢性阻塞性肺病的形成關系密切,因為它的缺乏,不能及時控制感染和炎癥產生的多種蛋白酶,而造成肺組織破壞。

α1-抗*由肝細胞產生,是一種分子量為45-56kDa的糖蛋白,它能抑制蛋白酶、彈性蛋白酶、膠原酶等多種水解酶的活性。
AAT也是一種糖蛋白,主要用于遺傳性AAT缺乏癥和良性惡性肝腫瘤、內胚竇瘤、組織細胞性淋巴瘤以及胰腺癌、胃癌、結腸癌等各種腫瘤的研究。此抗體與大、小鼠、狗和豬有交叉反應。

留言詢價/ MESSAGE INQUIRY

留言框

  • 產品:

  • 您的單位:

  • 您的姓名:

  • 聯系電話:

  • 常用郵箱:

  • 省份:

  • 詳細地址:

  • 補充說明:

  • 驗證碼:

    請輸入計算結果(填寫阿拉伯數字),如:三加四=7
掃碼加微信
021-60514606

地址:上海市滬閔路6088號龍之夢大廈8樓806室

服務熱線
18321282235

掃碼加微信

人人看人人摸人人干人人操| 蜜乳av牢记| 精品视频99| 精品一区二区无码| 精品久久国产| 波多野结衣一二三区| 未满十八勿进黄网站| 日韩无码网址| 国产成人一区| 亚洲一级毛片无码真人久久| 中文字幕一区二区三区| 国产精品无码粉嫩小泬| 亚洲AV综合色区无码| 欧美成人性爱视频免费电影| 91人妻中文字幕在线精品| 国产+日韩+国产| 91在线看视频| 久久精品无码一区二区三区| 黄色亚洲视频| 国产av网页| 狠狠的caoa| 亚洲亚洲人成综合网络| 亚洲欧美乱伦| 免费观看黄网站| 亚洲国产精选| 乱伦视频区91| 性欧美熟妇| 久久久久久国产精品| 国产欧美又粗又猛又爽| 91久久精品一区二区别| 国产又粗又猛视频免费| 久一在线| 米奇影视| 性虎精品一区二区三区| 无码精品电影| 日韩在线一区二区三区| 国产精品 家庭乱伦| 亚洲精品午夜福利| 午夜无码视频| 精品国产乱码久久久久久影片| 尤物在线|