亚洲中文字幕特级毛片-亚洲制服丝袜中文字幕-亚洲制服丝袜在线观看-亚洲制服欧美自拍另类-免费一级黄色-免费一级国产生活片

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
日本特黄a级高清免费大片,成人在线欧美亚洲,国自产拍亚洲免费视频
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-FYCO1/BF647 Conjugated antibody (bs-13237R-BF647)
訂購熱線:400-901-9800
訂購郵箱:sales@www.chomd.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.chomd.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-13237R-BF647
英文名稱 Rabbit Anti-FYCO1/BF647 Conjugated antibody
中文名稱 BF647標記的鋅指蛋白FYCO1抗體
別    名 DKFZp779K1152; FLJ13335; FYCO1; FYCO1_HUMAN; FYVE and coiled coil domain containing 1; FYVE and coiled coil domain containing protein 1; FYVE and coiled-coil domain-containing protein 1; MGC126517; MGC126519; RUFY3; RUN and FYVE domain containing 3; Zinc finger FYVE domain-containing protein 7.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 腫瘤  轉錄調節因子  鋅指蛋白  表觀遺傳學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, )
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 167kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human FYCO1
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.
產品介紹 background:
FYCO1 is a 1,478 amino acid protein that contains one RUN domain, one GOLD domain and one FYVE-type zinc finger. Expressed in heart and skeletal muscle, FYCO1 exists as multiple alternatively spliced isoforms and may play a role in transcriptional regulation events. In response to DNA damage, FYCO1 is subject to phosphorylation, probably by ATM or ATR. The gene encoding FYCO1 maps to human chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.

Function:
May mediate microtubule plus end-directed vesicle transport.

Subunit:
Can form homodimers. Interacts (via C-terminus) with MAP1LC3B. Interacts with RAB7A; the interaction with RAB7A induces FYCO1 recruitment to late endosomal/lysosomal compartments.

Subcellular Location:
Cytoplasmic vesicle, autophagosome. Endosome. Lysosome. Note=Localizes to the external but not to the internal membrane of autophagosomes, and upon autophagosome/late endosome/lysosome fusion, it stays on the external surface of autolysosomes.

Tissue Specificity:
Expressed in heart and skeletal muscle.

Post-translational modifications:
Phosphorylated upon DNA damage, probably by ATM or ATR.

DISEASE:
Defects in FYCO1 are the cause of cataract congenital autosomal recessive type 2 (CATC2) [MIM:610019]. An opacification of the crystalline lens of the eye becoming evident at birth or in infancy. It frequently results in visual impairment or blindness. Opacities vary in morphology, are often confined to a portion of the lens, and may be static or progressive. In general, the more posteriorly located and dense an opacity, the greater the impact on visual function. Note=Pathogenic mutations in FYCO1 can affect intracellular transport of autophagocytic vesicles from the perinuclear area to the periphery, leading to an accumulation of large numbers of vesicles and hence loss of lens transparency (PubMed:21636066).

Similarity:
Contains 1 FYVE-type zinc finger.
Contains 1 GOLD domain.
Contains 1 RUN domain.

Database links:
UniProtKB/Swiss-Prot: Q9BQS8.3

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.www.chomd.com.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: 羞羞国产一区二区三区四区视频入口 | 人妻无码中文字幕A V| 日本综合伊人色鬼久久| 精品久久久久久久亚洲综合网站 桃儿 | 伊人精品综合午| 无码精品人妻一区二区三区ap小说 | 91在线无码精品秘?入口91| 亚洲精品中文字幕乱码三区,久久 亚洲精品中文字幕乱码三区91_欧美一级 | 人妻日韩在线全网| 国产v片在线观看高清 | 成人免费一区二区三区四区五区六区黄色影视 | 亚洲高清欧美字幕中山文香| 久久久久国产午夜精品AⅤ| baby直播网站下载| 色婷婷综合久久久久中文一区二区三| 精品少妇一区二区三区视频亚洲.....| 99精品久久精品一区二区娜| 无码少妇中文字幕 果传媒| 国产综合成人久久大片91,亚洲国产成人久久综 | 久久996热精品996| 樱桃视频成人 在线观看免费| 日韩精品专区在线影院重磅_日韩精品一区二区亚洲AV | 精品久久久无码午夜福利不卡电动炮 | 91亚洲精品久久久久久久久久久久| 亚洲护士在线一卡在线播放| 国模少妇一区二区三区绯色| 亚洲中文字幕av无码人妻| 久久99久久99精品免观看软件色情少妞| 91视频电影网一区| 久久精品亚洲AV无码毛笔的用法| 中文字幕无乱码高清视频在线看| 全免费A级毛片免费看无码| 91精品久久久老熟女九色91| 另类免费视频一区二区在线观看不卡 | 好爽毛片一区二区三区四ai宋雨琦 | 国产网站在线播放视频大全| 亚洲国产一二三精品无码绿巨人南波杏 | 国产色在线观看免费视频勾搭女技师| 亚洲精品无码久久千人斩人妻中文字幕| 久久久一本精品99久久精品99欧美| 中文字幕日韩一区二区三区不卡久青草人妻|