超碰97自拍_久久99久久98精品免观看软件_在线亚洲一区_九九视频这里只有精品_国产精品一区二区欧美视频_精品国产区一区

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  聯系我們
逼逼导航,久久午夜夜伦鲁鲁片无码免费,69av色
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-LYPD1/BF647 Conjugated antibody (bs-18570R-BF647)
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 bs-18570R-BF647
英文名稱 Rabbit Anti-LYPD1/BF647 Conjugated antibody
中文名稱 BF647標記的LYPD1蛋白抗體
別    名 FLJ41033; LY6/PLAUR domain containing 1; Ly6/PLAUR domain-containing protein 1; Lypd1; LYPD1_HUMAN; LYPDC1; MGC29643; PHTS; Putative HeLa tumor suppressor.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 細胞生物  細胞凋亡  表觀遺傳學  細胞膜蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Rabbit, )
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 13kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human LYPD1
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 癈 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癈. 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 癈.
產品介紹 background:
LYPD1 is a 141 amino acid protein that contains one UPAR/Ly6 domain. LYPD1 is a cell membrane protein expressed as three isoforms and encoded by a gene mapping to human chromosome 2. As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr鰉 syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.

Subcellular Location:
Cell membrane.

Similarity:
Contains 1 UPAR/Ly6 domain.

Database links:

Entrez Gene: 116372 Human

Entrez Gene: 72585 Mouse

Entrez Gene: 360838 Rat

Omim: 610450 Human

SwissProt: Q8N2G4 Human

SwissProt: Q8BLC3 Mouse

SwissProt: Q66H42 Rat

Unigene: 432395 Human

Unigene: 741324 Human

Unigene: 490405 Mouse

Unigene: 231867 Rat



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 www.ggggww.cn 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
主站蜘蛛池模板: 午夜裸体女人视频网站在线观看 | 老司机狠狠干 | 99视频一区二区三区 | 久久久er热这里只有精品2 | 欧美特级黄色 | 国产在线视频2019最新视频 | 曼谷av女郎 | a级片免费在线播放 | 亚洲综合免费视频 | 国产一级v片不卡在线 | 国产精品久久国产三级国电话系列 | 亚洲高清国产拍精品影院 | 精品人伦一区二区三区蜜桃免费 | 欧美亚洲日韩在线综合 | 黄页免费看| 久久在线观看视频 | 国产成人久久AV免费看 | 日本一二区免费 | 青草国产精品久久久久久久久 | 天天操操夜夜操 | 亚洲人成人一区二区三区 | 亚欧洲精品在线视频免费观看 | mmm·www看片免费观看 | 久久不见久久见免费影院WWW日本 | 国产精品第一区第27页 | 国产免费一级淫片a级中文 www.avtvtv.com新网址 | 国产成人亚洲欧美久久影院 | 伊人一区| 国产不卡一区二区在线观看 | 影音先锋中文字幕亚洲资源站 | 天天做夜夜做狠狠做 | 99国内精品久久久久 | 亂倫近親相姦中文字幕 | 日韩欧美国产视频 | 欧美在线三级艳情网站 | 日韩精品人妻系列无码专区免费 | 免费爱爱小视频 | 午夜影院黄色 | 成人无码www免费视频嘿嘿软件 | 精品日本高清在线播放 | 欧美综合色网 |