產(chǎn)品編號 | bsm-52041R-Cy3 |
英文名稱 | Rabbit Anti-Collagen XVII/Cy3 Conjugated antibody |
中文名稱 | Cy3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. |
| 免费无码色情日本午夜视频 | 成人3D动漫一区二区三区91 | 美女裸体插振白浆糊涂 | 久久久久人妻精品365 | 亚洲一区二区三区四区五区不卡 | 波多野结衣乳巨码在线直播 | 国产成人一区二区三区别 | 丰满人妻熟妇乱又伦精品凤鸣阁 | 欧美XXXX黑人XXXX爽 | A级成人婬片免费看 | 日本视频免费观看 | 国产亚洲综合一区二区 | 欧美搡大BBBB流水 | 国產又粗又猛又爽又黄 | 国产无遮挡无黄又爽农村妇女 | 四川少妇BBB搡BBB搡多人乱亂 | 四川少妇BBBB槡BBBB槡 | 香蕉97人妻免费碰碰碰 | 久久免费精品视频 | 四川少妇女BBB凸凸凸凸 | A片人人澡C片人人人妻 | 白嫩小泬BBB免费观看 | 红桃视频网站一区二区精品 | 国产寡妇婬乱A毛片视频中文 | 国产91精品人妻互换tp | 亚州精品一区二区三区黄久 | 成人试看120秒体验区 | 四川BBB又粗又硬又大 | 美女丝袜一区二区三区 | 成人网站在线播放 | 国产成人小视频在线 | 欧美日韩中文字幕 | 免费无码婬片aaaa | 不要,不要黄色成人视频免费观看 | 欧美与黑人午夜性猛交久久久 | 亚洲成人AV有码一区 | 在线观看成年人网站污 | 欧美做爰性猛交XXXⅩ | 99在线视频免费观看 | 国产无码在线观看黄 |