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 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
国产无码老师机在线观看 | 免费在线观看黄片 | 日本一级特黄aa大片 | 成人精品一区二区三区A片用毒蛇 | 国产高潮的无套A片激情视频大全 | 色欲多多精品亚洲A | 亚洲无码高清福利视频 | www..com大插蕉 | 真实国产乱子伦精品一区二区 | 天天日天天射天天干 | 无套内谢少妇毛片A免费看 四川一级婬片60分钟A片 | 国产婬乱片A片AAA毛姪片 | 欧美BBBB嗽BBB爽 | 亚洲在线免费观看 | 99re这里只有精品6 | 国产日产久久久久久 | 91精品乱码久久蜜桃麻豆 | 西西大胆人体拍拍视频 | 欧美老妇AⅤ片AAAA片 | 啊啊讨厌舒服深一点视频 | 成人A片产无码免费视频奶头软件 | 欧美激情婬妇A片AAA毛多水多 | 久久视频一区二区三区 | 四川少妇搡BBB搡BBB搡多人伦 | 婷婷四房综合激情五月 | 91.www在线观看 | 亚洲日韩精品无码一区 | 中文字幕亚州无码强奸乱伦亚州有码 | 日本人妻伦在线中文字幕 | 久久成人麻豆午夜电影 | 国产精品扒开腿做爽爽爽A片小说 | 69人人人人人人人人人 | 国产免费人做人爱 | 免费一级婬片A片久久妖精97 | 特级婬片A片AAA毛片咕噜咕噜 | 人妻丰满熟妇AV无码 | 欧美揉BBBBB揉BBBBB | 特级丰满少妇一级AAAA爱毛片 | 北京熟妇槡BBBB槡BBBB一 | 免费国产一区二区三区 | 西西4444WWW大胆无视频 |