91精品少妇一区二区三区蜜桃臀,少妇搡BBBB搡BBB搡失恋,BBB片一毛片A片AA少妇,国产成人无码久久久久毛片朴信惠
掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  關于我們  聯(lián)系我們
久久人妻嫩草无码AV专区动漫,国产中文字幕在线观看,波多野结衣乳巨码无在线观看
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-Collagen XVII/PE-Cy7 Conjugated antibody (bsm-52041R-PE-Cy7)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bsm-52041R-PE-Cy7
英文名稱 Rabbit Anti-Collagen XVII/PE-Cy7 Conjugated antibody
中文名稱 PE-Cy7標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  
研究領域 細胞生物  信號轉導  
抗體來源 Rabbit
克隆類型 Monoclonal
克 隆 號 1C11
交叉反應 (predicted: Human, Mouse, Rat, )
產品應用 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.
版權所有 2004-2026 m.rvdoil.com 北京博奧森生物技術有限公司
通過國際質量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
通過國際醫(yī)療器械-質量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號: CQC24QY10047R0M/1100
京ICP備05066980號-1         京公網安備110107000727號
国产2018影视视频在线不卡免费看 | 人妻少妇孑伦无码视频 | 亚洲国产91精品A∨无码 | 国产一区二区三区操逼不卡视频 | 黄色视频在线下载观看 | 日韩精品一区二区三区四区五区 | 日婬片A片AAA毛片在线少妇 | 老熟女又肥又大黑BBB | 欧美日韩中文字幕 | 哈尔滨熟女白浆91九色 | 黑人A片无码看免看一生 | 北京熟妇搡BBBB搡BBBB | 亚洲AV无码乱码 | 户外露出自慰一区二区 | 老司机午夜福利私人定制 | 五十路潮吹免费视频 | 欧美黄色成人视频 | 真人做爰试看120秒 日韩精品一区二区无码 | 我要的网站欧美性欧美性欧美性欧美性 | 国产一级婬片A片免费无成人黑豆 | 亚洲人精品一区二区三区 | 日韩一区二区在线观看 | 成熟丰满熟妇av无码区四季 | 四川少妇BBB搡BBB爽爽爽 | 久久国产精品99久久人人澡 | 国产精品 日本 欧美 | 午夜性色福利影院 | 日批视频在线免费观看 | 中文字幕不卡少妇 无 | 欧洲国产一区免费观看 | 亚洲一区二区三区视频在线 | 四川BBBB搡BBB搡B1图 | 欧美日韩另类暴露女视频 | 国产99在线观看 | xfplay 无码视频 | 久久 91 人妻交换 日韩欧美 | 91拍真实国产伦偷精品 | 国产亚洲分享在线视频 | 国产黄色片免费看 | 国产亲子乱婬一级A片 | 四川少妇BBB搡BBB搡多人乱亂 |