產(chǎn)品編號 | bs-23177R |
英文名稱 | SOX2 Rabbit pAb |
中文名稱 | 胚胎干細(xì)胞關(guān)鍵蛋白抗體 |
別 名 | transcriptional factor SOX2; ANOP3; cb236; delta EF2a; lcc; MCOPS3; MGC148683; MGC2413; RGD1565646; Sex determining region Y box 2; Sex determining region Y-box 2; SOX 2; SRY(sex determining region Y) box 2; SRY box containing gene 2; SRY related HMG box |
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Specific References (1) | bs-23177R has been referenced in 1 publications.
[IF=6.684] Yao Jiang. et al. Atlas of Prenatal Hair Follicle Morphogenesis Using the Pig as a Model System. Front Cell Dev Biol. 2021; 9: 721979 IF ; Pig.
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研究領(lǐng)域 | 腫瘤 細(xì)胞生物 神經(jīng)生物學(xué) 干細(xì)胞 |
抗體來源 | Rabbit |
克隆類型 | Polyclonal |
交叉反應(yīng) | Human,Mouse,Rat (predicted: Sheep,Cow,Chicken,Dog,Horse) |
產(chǎn)品應(yīng)用 | WB=1:500-2000
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
理論分子量 | 34 kDa |
檢測分子量 | |
細(xì)胞定位 | 細(xì)胞核 細(xì)胞漿 |
性 狀 | Liquid |
濃 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human SOX2: 221-317/317 |
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 |
This intronless gene encodes a member of the SRY-related HMG-box (SOX) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The product of this gene is required for stem-cell maintenance in the central nervous system, and also regulates gene expression in the stomach. Mutations in this gene have been associated with optic nerve hypoplasia and with syndromic microphthalmia, a severe form of structural eye malformation. This gene lies within an intron of another gene called SOX2 overlapping transcript (SOX2OT). [provided by RefSeq, Jul 2008]. Function: Transcription factor that forms a trimeric complex with OCT4 on DNA and controls the expression of a number of genes involved in embryonic development such as YES1, FGF4, UTF1 and ZFP206 (By similarity). Critical for early embryogenesis and for embryonic stem cell pluripotency. May function as a switch in neuronal development. Downstream SRRT target that mediates the promotion of neural stem cell self-renewal (By similarity). Keeps neural cells undifferentiated by counteracting the activity of proneural proteins and suppresses neuronal differentiation. Subunit: Interacts with ZSCAN10. Interacts with SOX3 and FGFR1. Subcellular Location: Nucleus. Post-translational modifications: Sumoylation inhibits binding on DNA and negatively regulates the FGF4 transactivation. DISEASE: Defects in SOX2 are the cause of microphthalmia syndromic type 3 (MCOPS3) [MIM:206900]. Microphthalmia is a clinically heterogeneous disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues (anophthalmia). In many cases, microphthalmia/anophthalmia occurs in association with syndromes that include non-ocular abnormalities. MCOPS3 is characterized by the rare association of malformations including uni- or bilateral anophthalmia or microphthalmia, and esophageal atresia with trachoesophageal fistula. Similarity: Contains 1 HMG box DNA-binding domain. SWISS: P48431 Gene ID: 6657 Database links: Entrez Gene: 6657 Human Entrez Gene: 20674 Mouse Omim: 184429 Human SwissProt: P48431 Human SwissProt: P48432 Mouse Unigene: 518438 Human Unigene: 65396 Mouse Embryonic Stem Cell Marker (胚胎干細(xì)胞標(biāo)志物) 轉(zhuǎn)錄因子:胚胎干細(xì)胞相關(guān)蛋白Sox2是sox基因家族的一個成員,Sox2與Oct4、Nanog一樣是胚胎干細(xì)胞重要的轉(zhuǎn)錄因子,是維持干細(xì)胞特性中起到重要的作用因子;由于它在早期胚胎發(fā)生、神經(jīng)分化和晶狀體發(fā)育等多種重要的發(fā)育事件中都起著關(guān)鍵的作用,從而引起了越來越廣泛的關(guān)注。 |
產(chǎn)品圖片 | |
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