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轉(zhuǎn)錄因子SOX10重組兔單克隆抗體

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 中文名稱 轉(zhuǎn)錄因子SOX10重組兔單克隆抗體 

別    名 DOM; MGC15649; SOX 10; SOX10_HUMAN; SRY (sex determining region Y) box 10; SRY box containing gene 10; SRY related HMG box gene 10; Transcription factor SOX 10; Transcription factor SOX-10; WS4.   
研究領(lǐng)域 細胞生物  免疫學(xué)  神經(jīng)生物學(xué)  干細胞  細胞凋亡  表觀遺傳學(xué)   
抗體來源 Rabbit 
克隆類型 Monoclonal 
克 隆 號 26D7 
交叉反應(yīng) (predicted: Human, Mouse, Rat, ) 
產(chǎn)品應(yīng)用 WB=1:500-1000 IP=1:20-100 IHC-P=1:50-200 IHC-F=1:50-200 ICC=1:50-200 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. 
分 子 量 50kDa 
細胞定位 細胞核 細胞漿  
性    狀 Liquid 
濃    度 1mg/ml 
免 疫 原 Recombinant human SOX10 protein (350-450aa):  
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 Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. 
PubMed PubMed 
產(chǎn)品介紹 This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional activator after forming a protein complex with other proteins. This protein acts as a nucleocytoplasmic shuttle protein and is important for neural crest and peripheral nervous system development. Mutations in this gene are associated with Waardenburg-Shah and Waardenburg-Hirschsprung disease. [provided by RefSeq, Jul 2008]
 
Function:
Transcription factor that seems to function synergistically with the POU domain protein TST-1/OCT6/SCIP. Could confer cell specificity to the function of other transcription factors in developing and mature glia.
 
Subcellular Location:
Cytoplasm. Nucleus
 
Tissue Specificity:
Expressed in fetal brain and in adult brain, heart, small intestine and colon.
 
DISEASE:
Defects in SOX10 are the cause of Waardenburg syndrome type 2E (WS2E) [MIM:611584]. WS2 is a genetically heterogeneous, autosomal dominant disorder characterized by sensorineural deafness, pigmentary disturbanc
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