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★四分子交聯(lián)體9/四旋蛋白抗體品牌 分子生物學(xué)：質(zhì)粒抽提、PCR、Q-PCR、RT-PCR、分子生物學(xué)：基因合成、引物合成、基因測(cè)序、載體構(gòu)建等

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四分子交聯(lián)體9/四旋蛋白抗體品牌 英文名稱  Anti-TSPAN9/NET-5

中文名稱  四分子交聯(lián)體9/四旋蛋白抗體品牌 

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.

產(chǎn)品屬性：

濃    度  1mg/1ml

規(guī) 格  0.2ml/200μg

抗體來(lái)源  Rabbit

克隆類型   polyclonal

交叉反應(yīng)   Human, Mouse, Rat, Dog, Pig, Rabbit

產(chǎn)品類型   一抗  

研究領(lǐng)域    細(xì)胞生物 通道蛋白 細(xì)胞表面分子 細(xì)胞分化

蛋白分子量  predicted molecular weight: 26kDa 

性    狀   Lyophilized or Liquid

免 疫 原  KLH conjugated synthetic peptide derived from human TSPAN9

亞    型  IgG

純化方法   affinity purified by Protein A

儲(chǔ) 存 液   Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4

四分子交聯(lián)體9/四旋蛋白抗體品牌 產(chǎn)品應(yīng)用   WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 Flow-Cyt=1:20-100 IF=1:50-200

（石蠟切片需做抗原修復(fù)） 

 not yet tested in other applications.

 optimal dilutions/concentrations should be determined by the end user.  

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. 

Important Note  This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. 

產(chǎn)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.

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新：產(chǎn)品更新速度較快，基本上每周都有新產(chǎn)品出現(xiàn)。

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