產(chǎn)品編號 | bsm-52041R-Cy5.5 |
英文名稱 | Rabbit Anti-Collagen XVII/Cy5.5 Conjugated antibody |
中文名稱 | 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, 0.01M PBS, pH 7.4. |
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. |
| 国产精品一级毛片无码小说 | 欧美人做人爱无码视频 | 少妇做爰免费8级A片 | 四川少妇BBBBBB爽爽爽欧美 | 国产成人污视频网站 | 久久性爱高潮高清完整版免费观看 | 黄色视频网站赤裸网站 | 久久久中国中老人黄色视频 | 亚洲五十路熟妇A∨ | 操美女自慰潮喷久久久 | 那种视频在线观看亚洲 | 色情午夜 码一区二区 | 亚洲国产精品综合久久99视频 | 中文字幕熟女人妻偷伦 | 久久久人人爽爆乳A片 | 黄色无碼小视频在线观看 | 另类老妇性BBwBBw | 国产A级婬片A片免费妖精 | 四川少妇一级AAAAA片 | 亚洲AV吞精久久久久 | 亚洲精品久久久久久久久久久久久 | 久久久久亚洲AV无码专区男同 | BBwBBw性老妇BBwBBw| 国产又粗又猛视频 | 中国一级毛片免费播放 | 在线成人 视频嗯嗯啊 | 影音先锋AV成人资源站在线播放 | 成人在线免费视频 | 美女裸体露出无遮挡国产在线播放 | 欧美性做爰又大又粗又长 | 91麻豆精品A片国产在线观看 | 亚洲AV无码免费在线观看 | 午夜丰满极品美女A片 | 精品无码人妻口爆日本欧美 | 国产成人精品AA毛片 | 国精产品秘 福利姬入口 | 红桃视频一区二区三区四区 | 欧美丰满少妇人妻精品 | 四川少妇bbw搡bbbb搡bbbb 国产人妻 9 9精品无码一区李宗瑞 | 日本熟妇无码一区二区 |