產(chǎn)品編號 | bsm-52041R-Cy5 |
英文名稱 | Rabbit Anti-Collagen XVII/Cy5 Conjugated antibody |
中文名稱 | Cy5標(biāo)記的重組兔抗膠原蛋白17單克隆抗體 |
別 名 | Bullous Pemphigoid 180; 180 kDa bullous pemphigoid antigen 2; Alpha 1 type XVII collagen; BA16H23.2; BP 180; BP180; BPAG 2; BPAG2; Bullous pemphigoid antigen 2; COL17A1; Collagen 17; Collagen alpha 1 XVII chain; Collagen alpha 1(XVII) chain; Collagen alpha1 XVII chain; Collagen type XVII alpha 1; Collagen XVII alpha 1 polypeptide; CollagenXVII; Epidermolysis bullosa junctional localisata variant; FLJ60881; KIAA0204; LAD 1; LAD. |
規(guī)格價格 | 100ul/2980元 購買 大包裝/詢價 |
說 明 書 | 100ul |
研究領(lǐng)域 | 細(xì)胞生物 信號轉(zhuǎn)導(dǎo) |
抗體來源 | Rabbit |
克隆類型 | Monoclonal |
克 隆 號 | 1C11 |
交叉反應(yīng) | (predicted: Human, Mouse, Rat, ) |
產(chǎn)品應(yīng)用 | ICC=1:50-200 IF=1:50-200
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
分 子 量 | 150kDa |
性 狀 | Lyophilized or Liquid |
濃 度 | 1mg/ml |
免 疫 原 | Recombinant human Collagen XVII protein |
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. |
產(chǎn)品介紹 |
background: This gene encodes the alpha chain of type XVII collagen. Unlike most collagens, collagen XVII is a transmembrane protein. Collagen XVII is a structural component of hemidesmosomes, multiprotein complexes at the dermal-epidermal basement membrane zone that mediate adhesion of keratinocytes to the underlying membrane. Mutations in this gene are associated with both generalized atrophic benign and junctional epidermolysis bullosa. Two homotrimeric forms of type XVII collagen exist. The full length form is the transmembrane protein. A soluble form, referred to as either ectodomain or LAD-1, is generated by proteolytic processing of the full length form. [provided by RefSeq, Jul 2008] Function: Unlike most collagens, collagen XVII is a transmembrane protein. Collagen XVII is a structural component of hemidesmosomes, multiprotein complexes at the dermal epidermal basement membrane zone that mediate adhesion of keratinocytes to the underlying membrane. Mutations in the gene coding for collagen XVII are associated with both generalized atrophic benign and junctional epidermolysis bullosa. Two homotrimeric forms of type XVII collagen exist. The full length form is the transmembrane protein. A soluble form, referred to as either ectodomain or LAD 1, is generated by proteolytic processing of the full length form. Two transcript variants, one resulting from alternative splicing in the 3' UTR, have been identified for this gene. Subunit: Homotrimers of alpha 1(XVII)chains. Interacts (via cytoplasmic region) with ITGB4 (via cytoplasmic region). Interacts (via cytoplasmic region) with DST isoform 3 (via N-terminus). Interacts (via N-terminus) with PLEC. Interacts (via cytoplasmic region) with DSP. Subcellular Location: Cell junction, hemidesmosome. Membrane; Single-pass type II membrane protein. Note=Localized along the plasma membrane of the hemidesmosome. 120 kDa linear IgA disease antigen and 97 kDa linear IgA disease antigen: Secreted, extracellular space, extracellular matrix, basement membrane. Post-translational modifications: The intracellular/endo domain is disulfide-linked. DISEASE: Generalized atrophic benign epidermolysis bullosa (GABEB) [MIM:226650]: A non-lethal, adult form of junctional epidermolysis bullosa characterized by life-long blistering of the skin, associated with hair and tooth abnormalities. Note=The disease is caused by mutations affecting the gene represented in this entry. Database links: Entrez Gene: 1308 Human Omim: 113811 Human SwissProt: Q9UMD9 Human Unigene: 117938 Human Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| 西西4444WWW无码视频 | 国产精品三区在线观看 | 91丨PORN丨人妻偷人 | 无码精品秘 人口一区二区 91人妻人人做人碰人人爽 | 欧美成人精品一级A片青椒视频 | 久久久久成人精品无码 | 麻豆乱码国产一区二区三区 | 四川丰满少妇一级A片 | ...高潮太爽日本产无人区 | 又大又粗又硬又猛又黄的高朝视频 | 人妻aⅴ无码一区二区三区 精品乱码一区内射人妻无码 | 欧美按摩做爰AAAAA | 成人爱爱视频免费在线播放 | 中文字幕一区二区三区伦理影院 | 熟妇少妇自拍偷拍第五页 | 玩两个丰满老熟女久久网 | 中文字幕-在线观看-黄色区 | 91亚洲精品久久久久蜜桃 | 国产精品福利在线 | 粗大的内捧猛烈进出A片 | jiqingxiaoshuo综合婷婷 | 黄色视频网站免费观看 | 又粗又大又硬毛片免费看 | 亚洲精品日韩精品 | 全免费A级毛片免费看网站招嫖 | 无遮挡毛片免费观看视频 | 无码人妻一区二区三区免费京洛会 | 前田香织无码一区二区 | 影音先锋制服丝袜 | 国产精品自拍红桃视频 | 国产黄色视频在线观看视频 | 久久久久久久av | www.eeuss| 国产成人精品麻豆传奇 | 亚洲AⅤ无码一区二区波多野按摩 | 四川乱子伦视频国产 | 成人做爰A片免费看视频 | 四虎视频成人版黄A片 | 精品久久久久久成人AV | 18 精品 爽爽国产在线观右手 |