成人av免费在线观看专区-亚洲综合五月久久丁香-男人天堂黄色国产精品-欧美国产精品乱子码一区二区三区

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(lián)系我們
日韩三级 久久久久久,夜夜躁狠狠躁日日躁视频传媒,亚洲乱色熟女一区二区蜜臀
首頁 > 產品中心 > 一抗 > 產品信息
TSPAN9 Rabbit pAb (bs-9448R)  
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-9448R
英文名稱 TSPAN9 Rabbit pAb
中文名稱 四分子交聯(lián)體9/四旋蛋白抗體
別    名 Tetraspanin 9; NET 5; NET5; PP1057; Tetraspan NET 5; Tetraspan NET-5; Tetraspanin-9; Transmembrane 4 superfamily member tetraspan NET 5; TSN9_HUMAN; Tspan-9; TSPAN9.  
研究領域 細胞生物  通道蛋白  細胞表面分子  細胞分化  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human (predicted: Mouse,Rat,Rabbit,Pig,Dog)
產品應用 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 27 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 TSPAN9: 131-239/239 <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 The tetraspanin family is a group of cell surface proteins that regulate cell development, activation, growth and motility. Each member contains four hydrophobic domains and participates in the mediation of signal transduction. NET-5, also known as TSPAN9 (tetraspanin 9), is a 239 amino acid multi-pass membrane protein that belongs to the tetraspanin (TM4SF) family. NET-5 forms a complex with GPVI in the tetraspanin microdomains on the platelet surface, and is encoded by a gene that maps to human chromosome 12p13.33. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.

Subunit:
Found in a complex with GP6.

Subcellular Location:
Membrane; Multi-pass membrane protein.

Tissue Specificity:
Expressed in megakaryocytes and platelets.

Similarity:
Belongs to the tetraspanin (TM4SF) family.

SWISS:
O75954

Gene ID:
10867

Database links:

Entrez Gene: 10867 Human

Omim: 613137 Human

SwissProt: O75954 Human

Unigene: 504517 Human



版權所有 2004-2026 lt325.com 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(yī)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