强伦轩一级A片在线观看,中文字幕乱码人妻二区三区,鲁鲁狠狠狠7777一区二区,西西4444www无码精品
掃碼關(guān)注公眾號(hào)           掃碼咨詢技術(shù)支持           掃碼咨詢技術(shù)服務(wù)
  
客服熱線:400-901-9800  客服QQ:4009019800  技術(shù)答疑  技術(shù)支持  質(zhì)量反饋  關(guān)于我們  聯(lián)系我們
安徽少妇BBBB搡BBBB,日韩欧美在线播放,亚洲一区二区三区在线
Rabbit Anti-TWIST/PE-Cy5 Conjugated antibody (bs-2441R-PE-Cy5)
訂購(gòu)熱線:400-901-9800
訂購(gòu)郵箱:sales@bioss.com.cn
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
說(shuō) 明 書(shū): 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-2441R-PE-Cy5
英文名稱 Rabbit Anti-TWIST/PE-Cy5 Conjugated antibody
中文名稱 PE-Cy5標(biāo)記的TWIST蛋白抗體
別    名 ACS3; B-HLH DNA binding protein; bHLHa38; BPES2; BPES3; Class A basic helix-loop-helix protein 38; CRS1; H-twist; OTTHUMP00000116043; SCS; Twist basic helix loop helix transcription factor 1; Twist homolog 1 (Drosophila); Twist homolog 1; TWIST homolog of drosophila; Twist related protein 1; Twist-related protein 1; Twist1; TWST1_HUMAN.  
規(guī)格價(jià)格 100ul/2980元 購(gòu)買        大包裝/詢價(jià)
說(shuō) 明 書(shū) 100ul  
研究領(lǐng)域 腫瘤  免疫學(xué)  神經(jīng)生物學(xué)  轉(zhuǎn)錄調(diào)節(jié)因子  
抗體來(lái)源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Human, Mouse,  (predicted: Rat, )
產(chǎn)品應(yīng)用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 23kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human TWIST
亞    型 IgG
純化方法 affinity purified by Protein A
儲(chǔ) 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(chǎn)品介紹 background:
Basic helix-loop-helix (bHLH) transcription factors have been implicated in cell lineage determination and differentiation. The protein encoded by this gene is a bHLH transcription factor and shares similarity with another bHLH transcription factor, Dermo1. The strongest expression of this mRNA is in placental tissue; in adults, mesodermally derived tissues express this mRNA preferentially. Mutations in this gene have been found in patients with Saethre-Chotzen syndrome. [provided by RefSeq, Jul 2008].

Function:
Acts as a transcriptional regulator. Inhibits myogenesis by sequestrating E proteins, inhibiting trans-activation by MEF2, and inhibiting DNA-binding by MYOD1 through physical interaction. This interaction probably involves the basic domains of both proteins. Also represses expression of proinflammatory cytokines such as TNFA and IL1B. Regulates cranial suture patterning and fusion. Activates transcription as a heterodimer with E proteins. Regulates gene expression differentially, depending on dimer composition. Homodimers induce expression of FGFR2 and POSTN while heterodimers repress FGFR2 and POSTN expression and induce THBS1 expression. Heterodimerization is also required for osteoblast differentiation.

Subunit:
Efficient DNA binding requires dimerization with another bHLH protein. Homodimer or heterodimer with E proteins such as TCF3. ID1 binds preferentially to TCF3 but does not interact efficiently with TWIST1 so ID1 levels control the amount of TCF3 available to dimerize with TWIST1 and thus determine the type of dimer formed.

Subcellular Location:
Nucleus.

Tissue Specificity:
Subset of mesodermal cells

DISEASE:
Defects in TWIST1 are a cause of Saethre-Chotzen syndrome (SCS) [MIM:101400]; also known as acrocephalosyndactyly type 3 (ACS3). SCS is a craniosynostosis syndrome characterized by coronal synostosis, brachycephaly, low frontal hairline, facial asymmetry, hypertelorism, broad halluces, and clinodactyly.
Defects in TWIST1 are the cause of Robinow-Sorauf syndrome (RSS) [MIM:180750]; also known as craniosynostosis-bifid hallux syndrome. RSS is an autosomal dominant defect characterized by minor skull and limb anomalies which is very similar to Saethre-Chotzen syndrome.
Defects in TWIST1 are the cause of craniosynostosis type 1 (CRS1) [MIM:123100]. Craniosynostosis consists of premature fusion of one or more cranial sutures, resulting in an abnormal head shape.

Similarity:
Contains 1 basic helix-loop-helix (bHLH) domain.

Database links:

Entrez Gene: 7291 Human

Entrez Gene: 22160 Mouse

Entrez Gene: 85489 Rat

Omim: 601622 Human

SwissProt: Q15672 Human

SwissProt: P26687 Mouse

Unigene: 66744 Human

Unigene: 3280 Mouse

Unigene: 161904 Rat



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

轉(zhuǎn)錄因子
Twist蛋白是屬于堿性螺旋-環(huán)-螺旋蛋白家族中的高度保守的轉(zhuǎn)錄因子,Twist在抑制腫瘤凋亡,促進(jìn)腫瘤細(xì)胞的轉(zhuǎn)移發(fā)揮一定的作用。
版權(quán)所有 2004-2026 m.nmgps.com 北京博奧森生物技術(shù)有限公司
通過(guò)國(guó)際質(zhì)量管理體系ISO 9001:2015 GB/T 19001-2016    證書(shū)編號(hào): 00124Q34771R2M/1100
通過(guò)國(guó)際醫(yī)療器械-質(zhì)量管理體系ISO 13485:2016 GB/T 42061-2022    證書(shū)編號(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
国产乱XXⅩXX国语对白 | 免费国偷拍精品视频 | 69人妻精品丰满熟女区 | 日韩人妻精品中文字幕 | 一级A片色情大片视频我和少妇 | 黄色成人网站在线观看 | 久久网正在播中文字幕 | 午夜久久人妻一级内射 | 日本大片在线观看 | 男同体育生乱Yin高H肉汁呻吟 | 国产一区波多野结衣 | 国产寡妇婬乱A毛片视频 | 公妇乱片A片免费看少妇直播麻豆 | 91人妻人人澡人人爽人人 | 久久免费看少妇高潮片A黄 国产AV无码AV高清AV | 农村乱人妻一区二区三区 | 中国女人和男的黄色视频 | 国产在线观看无码免费视频 | 欧美精黑人一级A片蜜桃视频 | 国产无人区码熟妇毛片多 | 亚洲精品秘 一区二区三区蜜桃久 | 久久综合精品一区二区三区 | 色情午夜 码一区二区 | 国产一级a毛一级a看免费视频黑人 | 国产成人精品无码视频18禁 | 安徽少妇BBBB搡BBBB | 国产人伦子伦一级A片下载 丰满人妻中伦妇伦精品久久 | 91精品国产aⅴ一区二区 | 国产亚洲色婷婷久久精品 | 成人亚洲A片V一区二区三区蜜月 | 国产欧美一区二区精品性色超碰 | 2019中文在线观看免费高清第三季预告 | 成人无码区免费A∨毛片 | 蜜桃秘 av无码一区二区三区 | 久久丫精品忘忧草西安产品 | 国产三级午夜理伦三级 | 成人A片产无码免费视频奶头软件 | 国产精品无码内射肛交 | 国产精品十八禁一区二区 | 蜜桃AV裸体美女被操潮吹 | 又粗又大成人片在线观看 |