强伦轩一级A片在线观看,中文字幕乱码人妻二区三区,鲁鲁狠狠狠7777一区二区,西西4444www无码精品
掃碼關(guān)注公眾號           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務(wù)
  
客服熱線:400-901-9800  客服QQ:4009019800  技術(shù)答疑  技術(shù)支持  質(zhì)量反饋  關(guān)于我們  聯(lián)系我們
少女哔哩哔哩视频在线看免费,国产精品伦子伦露脸
Rabbit Anti-Collagen XVII/Cy3 Conjugated antibody (bsm-52041R-Cy3)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
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.
版權(quán)所有 2004-2026 www.nmgps.com 北京博奧森生物技術(shù)有限公司
通過國際質(zhì)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(zhì)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(wǎng)安備110107000727號
红桃在线无码精品秘 入口色欲 | 四川少妇搡BBw搡BBBB搡 | 欧美成人午夜精品久久久 | 少妇婬妇又爽又紧又爽A片 99精品成人无码A片漫画 | 在线中文字幕av | 丰满岳乱妇一区二区三区 | 国产一区无码不卡电影 | 欧美偷伦无码一区二区 | 精品乱码一区二区三四 | 少妇搡BBBB搡BBBB毛多多 | 操美女视频在线观看 | 在线观看强奸美女视频网站大全 | 中文字幕无码A片一区在线观看 | 国产精品扒开脚做爽爽爽 | 免费无码又爽又高潮视频软件 | 国产无码av在线 | 美女视频在线观看黄色视频在线观看 | 大乳女被粗大的猛烈进出视频 | 国产熟妇婬乱一区二区 | 狼友91精品一区二区三区 | 懂色AV无码中字幕一区 | 欧美成人r级一级二级三级 国产人妻互换一级毛片日本 | 亚洲天堂在线观看无码 | 欧美最爽乱婬A片黑人 | 国产欧美在线观看不卡高清 | 在线观看中文字幕av | 亚洲 日韩 丝袜 熟女 变态 | 黄色无码在线观看免费 | 亚洲嫩模视频免费观看 | 无码精品黑人一区二区老人 | 国产婬片lA片久久久久久动漫 | 国产精品亚洲欧美日韩久久制服诱 | 91人妻人人搡人人爽 | 女人在线看片网站 | 亲妺妺乱的性视频播放 | 国内精品国产成人国产三级 | 无码人妻aⅴ一区二区三区有奶水 | 国产一区视频在线播放 | 俄罗斯无码成人午夜电影 | 国产激情视频在线观看 | 91精品人妻一区二区三区蜜桃 |