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(guān)注公眾號           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
最近最经典中文MV字幕,免费看一级一级人妻片,亚洲国产精品一区二区久久阿宾
Rabbit Anti-TWIST/PE-Cy3 Conjugated antibody (bs-2441R-PE-Cy3)
訂購熱線:400-901-9800
訂購郵箱:sales@bioss.com.cn
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@bioss.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-2441R-PE-Cy3
英文名稱 Rabbit Anti-TWIST/PE-Cy3 Conjugated antibody
中文名稱 PE-Cy3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)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 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 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 www.rvdoil.com 北京博奧森生物技術(shù)有限公司
通過國際質(zhì)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(zhì)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(wǎng)安備110107000727號
黑人亚洲精品A片久久99 | 亚洲Av免费在线观看 | 久久网正在播中文字幕 | 蜜臀AⅤ国产精品久久久国产老师 | 鲁大师免费观看日本电影 | EEUSS鲁片一区二区三区四虎 | 啊啊啊轻点亚洲一区 | 中文字幕av一区二区 | 国产一级a毛一级a爰片 | FUCK国产精品一区 | 无码不卡AV毛片久久婷 | AⅤ 国产 美女 白丝 | 美女口交吞精视频 | 日本麻豆黄色电影。 | 色综合久久天天综合网 | 日韩人妻精品无码久久 | 一本一道人妻久久久久久中文字幕 | 国产裸体美女永久免费视频 | AV网站在线免费观看 | 精品人妻无码一级A片 | 国产又黄又猛又粗又爽 | 少妇喷潮 固产 | 国产人妻人伦精品无码.麻豆 | 欧美韩国日本国产精品三级片视频 | 国产精品海角社区在线 | 国产成人愉拍精品久久 | 奶水人妻一区二区三区 | 欧美日韩国产在线 | 激情视频激情图片激情小说 | 金莲TV中文字幕亚洲 | 户外勾搭女人无套内谢 | 色情乱婬A片AAA毛多水多 | 亚洲人成人无码网www国产 | 特级西西人体4444XXXX | 91传媒视频网站在线观看 | 波多野结衣无码视频在线观看 | 精品国产精品三级精品AV网址 | 黑人又粗又大一级毛片多人做 | 成人女性A片在线观看仙踪林 | 蜜臀久久精品久久久久消防站 | 欧美日本一级a一片色达人提供 |