91精品少妇一区二区三区蜜桃臀,少妇搡BBBB搡BBB搡失恋,BBB片一毛片A片AA少妇,国产成人无码久久久久毛片朴信惠
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  聯系我們
www.国产精品,亚洲熟妇少妇熟女A片百度知道
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-SOX2/RBITC Conjugated antibody (bs-23177R-RBITC)
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
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-23177R-RBITC
英文名稱 Rabbit Anti-SOX2/RBITC Conjugated antibody
中文名稱 羅丹明(RBITC)標記的胚胎干細胞關鍵蛋白抗體
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 2; SRY related HMG box gene 2; SRY-box 2; ysb; SOX2_HUMAN; Transcription factor SOX-2; SOX2_HUMAN.  
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 腫瘤  細胞生物  神經生物學  干細胞  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Mouse, Rat,  (predicted: Human, Chicken, Dog, Pig, Cow, Horse, Rabbit, Sheep, )
產品應用 ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 32kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human SOX2
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 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.
產品介紹 background:
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.

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



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

Embryonic Stem Cell Marker (胚胎干細胞標志物)
轉錄因子:胚胎干細胞相關蛋白Sox2是sox基因家族的一個成員,Sox2與Oct4、Nanog一樣是胚胎干細胞重要的轉錄因子,是維持干細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)育事件中都起著關鍵的作用,從而引起了越來越廣泛的關注。
版權所有 2004-2026 m.rvdoil.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
91视频在线观看18 | 女人自慰冒白浆在线观看 | 91九色丨国产丨人妻在线 | 亚洲精品无码久久久 | 中文字幕永久在线 | 无码精品视频在线观看 | 免费在线观看91成人 | 无码国产精品一区二区高潮 | 黄色高清无码在线观看 | 91人妻人人做人碰人人爽九色-百度 | 一级做a爰片久久毛片无码免费 | 国产一级a毛一级a看免费人交 | 又粗又大又黄A片免费看樱花 | 亚洲AV成人无码久久精品麻豆 | 人妻久久久一区二区三区 | 韩国无码在线观看 | 91大神人妻论坛性趣 | 免费看污网站在线观看 | 日本激情网站在线观看 | 绝色丰满少妇无码A片 | 久久人妻精品色欲网站 | 国产伦精品一区二区三区男技 | av无码一区二区 | 日韩精品无码人妻第一页 | 人妻偷国产网曝门91 | 久久91欧美特黄A片 十五分钟高清无码视频 | 爆 喷水 洗澡 91 | 色国产精品女五丁香五月五月 | 苍井そら50分钟无码流出 | 亚国产精品婷婷久久久ww | 中文字幕无码黄色视频 | 亚洲精品久久久久毛片A级绿茶 | 无码-国产老妇伦国产熟 | 日本黑人乱偷人妻中文字幕 | 中文字幕日韩精品无码 | 免费无码婬A片在线视频夜场 | 国产清纯白嫩初高中在线观看性色 | 久久99久久99久久 | 少妇搡BBBB搡BBB搡失恋 | 人妻丰满熟妇一区二区三区 | 女人高潮特黄AAAAA片 |