97久久久精品综合88久久_亚洲国产精品一_久热热国产久热_97操操操_北条麻妃在线免费观看_精品国自产拍天天拍

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
99精品综合加勒比在线观,亚洲国产熟妇无码日韩,亚洲伊人成无码综合网
首頁 > 產品中心 > 一抗 > 產品信息
TMEM16C Rabbit pAb (bs-12479R)  
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
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價
產品編號 bs-12479R
英文名稱 TMEM16C Rabbit pAb
中文名稱 跨膜蛋白16C抗體
別    名 Anoctamin 3; ANO3; C11orf25; GENX 3947; TMEM16C; Transmembrane protein 16C(eight membrane spanning domains); Transmembrane protein 16C; ANO3_HUMAN; DYT23; DYT24; GENX-3947.  
研究領域 腫瘤  細胞生物  信號轉導  新陳代謝  跨膜蛋白  細胞膜蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
克 隆 號
交叉反應 (predicted: Human,Mouse,Rat,Rabbit,Pig,Sheep,Cow,Dog,Horse)
產品應用 WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 115 kDa
檢測分子量
細胞定位 細胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human TMEM16C/Anoctamin 3: 801-900/981 <Extracellular>
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 TMEM16C is a 981 amino acid multi-pass membrane protein that is encoded by a gene which maps to chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations, while Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.

Function:
Anoctamin 3 belongs to the anoctamin family. Anoctamin 3 may act as a calcium activated chloride channel.

Subcellular Location:
Membrane; Multi pass membrane protein.

Similarity:
Belongs to the anoctamin family.

SWISS:
Q9BYT9

Gene ID:
63982

Database links:

Entrez Gene: 63982 Human

Entrez Gene: 228432 Mouse

Entrez Gene: 100519534 Pig

Entrez Gene: 311287 Rat

Omim: 610110 Human

SwissProt: Q9BYT9 Human

SwissProt: A2AHL1 Mouse

SwissProt: F1SFZ6 Pig



版權所有 2004-2026 m.kastlife.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: 国产日女人 | 亚洲最新精品 | 午夜久操| 91无码视频在线观看 | 国产成人精品视频免费 | 婷婷久久国产对白刺激五月99 | 囯产精品久久久久久久久久妞妞 | 国产黑色丝袜在线视频 | 天天爱天天做天天添天天欢 | 久久综合五月天 | 久久中文字幕亚洲 | 青青草视频在线观 | 91狠狠综合| 欧美一级片久久 | 国产成人精品微拍视频网址 | 国产一区二区久久 | 欧美人与ZOXXXX乱叫 | 久久天堂一区二区三区 | 日韩亚洲欧美一区 | 狠狠操操 | 在线观看av每日更新免费 | 2023国精产品一二二线免费 | jizzjizz中国18大学生 | 变形金刚之超能勇士免费观看 | 2017最新高清无码网站 | 国产91免费看 | 精品国产乱码一区二区三区 | 国产日韩欧美一区二区三区乱码 | 深夜看国产毛片在线视频香蕉 | 久久999精品久久久有什么优势 | 国产九色在线观看 | 艳妇乳肉豪妇荡乳AV无码福利 | 国产日韩欧美一区 | 国产香蕉一区二区三区 | 久久久乱码精品亚洲日韩 | 91精品国产9 | 久久九九热 | 99热9 | 久久久久久久人妻无码中文字幕爆 | 久久免费视频国产 | 亚洲理论中文字幕 |