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
青青草国产,亚洲午夜久久久精品一区二区三剧 ,欧美国产综合
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-LYPD1/PE Conjugated antibody (bs-18570R-PE)
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-PE
英文名稱 Rabbit Anti-LYPD1/PE Conjugated antibody
中文名稱 PE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: 亚洲天堂福利视频 | 日本娇小xxxⅹhd | 91成品入口 | 四虎影音最新网址 | 亚洲乱码一卡二卡四卡乱码新区 | 无遮挡亲胸捏胸免费视频 | 欧产日产国产蜜网站 | 99热这里只有精品在线 | 亚洲一区二区三区视频播放 | 中文毛片 | 久久亚洲AV永久无码精品 | 国产精品久久久久精女同 | 欧美日韩国产成人在线91 | FREE性丰满HD毛多多 | 中文字幕永久视频在线看 | 中文字幕ˉ色哟哟 | 成人国产精品免费网站 | av在线播放资源 | 国产成人精品无码片区 | 天天综合亚洲色在线精品 | 香蕉视频在线观看亚洲 | 久久中文字幕无码一区二区 | 伊人亚洲精品 | 免费A级毛片 | 片多多免费观看高清 | 精品亚洲永久 | 成人区一区二区三区 | 97色国产 | www.青青草.com | 亚洲国产一区二区精品视频 | 久久久久久久久久久久久久久伊免 | 9999国产| 性色AⅤ在线观看免费 | 精品国产二区在线 | 在线超碰免费 | 99久久国产综合精麻豆 | 国产麻豆精品一区二区三区V视界 | 色综合九九 | 性久久久久久 | 精品毛片免费看 | 无码国产精品亚洲а∨天堂dvd |