產(chǎn)品編號 | bsm-52041R-PE-Cy5.5 |
英文名稱 | Rabbit Anti-Collagen XVII/PE-Cy5.5 Conjugated antibody |
中文名稱 | PE-Cy5.5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(jià)格 | 100ul/2980元 購買 大包裝/詢價(jià) |
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 | Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.05M PB, pH 7.5. |
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. |
| jk白丝护士一区二区三区 | 国产精产国品91在线看 | 俄罗斯一区二区无码 | 亚洲乱码日产精品BD | 亚洲国产无码AV三区 | 国产精品一区三区四区A片 欧美肥婆日逼视频免费播放 | 日本婬乱A片AAA毛片麻豆软件 | 无码人妻一区二区三区免费京洛会 | 美女裸体免费视频久久久 | 免费一级一级人妻a片 | 张丽一级婬片A片免费观看 西西人体大胆WWW444 | 日本无码人妻波多野结衣杨思敏 | 精品秘 无码一区二区三 | 无码区免费看一级毛片A片 久久精品www人人爽人人 | 丰满少妇理伦A片在线看 | 性感美女被操到高潮 | 国产BBB搡BBB爽爽爽电影 | 国产在线精品国自产拍 | 亚洲精品成a人在线观看 | 婬片艳片A片欧美精品极度变态 | 国产乱子子伦精品视频 | 国内精品人妻无码久久久影院蜜桃 | 亚洲福利小短视频在线看看 | 亚洲精品无码乱码成人果冻传媒 | 亚洲人妻中文字幕av | 久久久91人妻无码精品蜜桃ID | 无码人妻丰满熟妇啪啪欧美 | 中文字幕先锋影音 | 韩国国产在线视频 | 久久99偷拍视频 | 精品国产一区二区国模嫣然 | 少女哔哩哔哩免费观看视频 | 高清在线播放无码 | 亚洲一区二区视频在线观看 | 午夜亚洲欧美俄罗斯新网络 | 国产伦精品一区二区三区妓女原神 | 国产一级视频在线观看 | 欧美激情一区二区不卡 | 亚洲天堂毛片在线观看 | 少妇高潮灌满白浆毛片免费看 |