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Rabbit Anti-TALLA-1  antibody (bs-9416R)  
~~~促銷代碼KT202411~~~
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
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說明書: 50ul  100ul  200ul
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-9416R
英文名稱 Rabbit Anti-TALLA-1  antibody
中文名稱 T細(xì)胞急性淋巴母細(xì)胞白血病相關(guān)抗原1抗體
別    名 CD231 antigen; Cell surface glycoprotein A15; Membrane component X chromosome surface marker 1; T cell acute lymphoblastic leukemia associated antigen 1; TALLA 1; TALLA1; Tetraspanin 7; Tetraspanin-7; Transmembrane 4 superfamily member 2; Tspan 7; TSN7_HUMAN; Tspan-7; TALLA-1.  
研究領(lǐng)域 腫瘤  細(xì)胞生物  信號(hào)轉(zhuǎn)導(dǎo)  細(xì)胞表面分子  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human,Mouse,Rat,Rabbit,Pig,Sheep,Cow,Dog,Horse)
產(chǎn)品應(yīng)用 WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:50-200,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 28kDa
細(xì)胞定位 細(xì)胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Tetraspanin-7: 131-230/249 <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(xiàng) This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 Tetraspanins are a group of hydrophobic membrane proteins that interact with a wide variety of proteins including intracellular signaling molecules, integrins and membrane receptors. TSPAN7 (tetraspanin 7), also known as MXS1 (membrane component chromosome X surface marker 1) or TM4SF2 (transmembrane 4 superfamily member 2), is a 249 amino acid multi-pass membrane protein belonging to the tetraspanin (TM4SF) family of transmembrane proteins. TSPAN7 is believed to play a role in cell motility and cell proliferation. The gene that encodes TSPAN7 maps to human chromosome X and defects in this gene are a cause of mental retardation X-linked type 58 (MRX58), which is characterized by dramatically below average general intellectual functioning.

Function:
May be involved in cell proliferation and cell motility.

Subunit:
Interacts with herpes simplex virus 1 (HHV-1) UL35.

Subcellular Location:
Membrane; Multi-pass membrane protein.

Tissue Specificity:
Not solely expressed in T-cells. Expressed in acute myelocytic leukemia cells of some patients.

DISEASE:
Defects in TSPAN7 are the cause of mental retardation X-linked type 58 (MRX58) [MIM:300210]. Mental retardation is characterized by significantly sub-average general intellectual functioning associated with impairments in adaptative behavior and manifested during the developmental period. Non-syndromic mental retardation patients do not manifest other clinical signs.

Similarity:
Belongs to the tetraspanin (TM4SF) family.

SWISS:
P41732

Gene ID:
7102

Database links:

Entrez Gene: 7102 Human

Omim: 300096 Human

SwissProt: P41732 Human

Unigene: 441664 Human



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