產(chǎn)品編號(hào) | bsm-52041R-RBITC |
英文名稱 | Rabbit Anti-Collagen XVII/RBITC Conjugated antibody |
中文名稱 | 羅丹明(RBITC)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(gòu)買 大包裝/詢價(jià) |
說 明 書 | 100ul |
研究領(lǐng)域 | 細(xì)胞生物 信號(hào)轉(zhuǎn)導(dǎo) |
抗體來源 | Rabbit |
克隆類型 | Monoclonal |
克 隆 號(hào) | 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(chǔ) 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. |
| 亚洲精品无码久久久 | 草1024榴社区成人影院 | 欧美顶级黃色大片免费 | 黄色视频免费观看网站 | 国产精品 久久久精品软件 中文字幕在线观看一区二区 | 少妇精品久久久久久久久久 | 国产成人a亚洲精品 | 亚洲精品秘 无码一区二区软件 | 欧美性色XXⅩXXA片 | 国产天美欧美精品无码 | 国产色情无码一区二区百度云 | 国产特黄A片AAAA毛片 | 亚洲无码网站在线观看 | 蜜桃视频黄在线看17·c | 黄色三a三级国产色情无码 熟妇人妻中文字幕av无码 | 91.www在线观看 | 久久久午夜精品图片 | 无码国产传媒爱豆传媒人妻 | 9热视频这里只有精品 | 亚州精品一区二区视频网站 | 欧美搡大BBBB流水 | 免费体验爆乳美女爱爱视频 | 国产视频秘 福利姬在线 | 亚洲精品国产自在在线 | 无码人妻精品一桃在线看 | 黄色在线免费观看网站 | 四川少妇bbw搡bbbb搡bbbb 国产人妻 9 9精品无码一区李宗瑞 | 嫩草AV久久伊人妇女超级a | 欧洲美女淫妓A级高清视频播放 | 亚洲AV成人一区二区三区观看 | AA鲁丝片一区二区免费看 | 日本A V在线播放 | 国产一区二区三区在线视频 | 中文字幕乱近親相姦视频中出恩施 | 四虎无码在线精品一区二区 | 色欲AV性色av浪潮AV壹牛网 | 深夜老司机一区二区三区 | 国产A三级三级三级看三级 给我播放国产高清无码视频 | 久久久久久国产成人a亚洲精品无码 | 成人精品鲁一鲁一区二区 |