CAOPORN成人免费公开,欧美FREESEX黑人又粗又大 ,欧美狠狠入鲁的视频777色,主仆调教SM束缚绳索捆绑

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
国产精品偷伦视频免费观看了,亚洲AV成人片色在线观看高潮
Rabbit Anti-TWIST/PE-Cy7 Conjugated antibody (bs-2441R-PE-Cy7)
訂購熱線:400-901-9800
訂購郵箱:sales@www.tjshangbang.com
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@www.tjshangbang.com
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-2441R-PE-Cy7
英文名稱 Rabbit Anti-TWIST/PE-Cy7 Conjugated antibody
中文名稱 PE-Cy7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 購買        大包裝/詢價(jià)
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(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 www.www.tjshangbang.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(hào): 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(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
国产WW久久久久久久久久| 欧美日韩午夜视频| 在线激情无码免费看| 100至499| 久久精品A一国产成人免费网站| 亚洲欧美日韩人成在线播放| 亚洲成a人v欧美综合天堂下载| 日本一区午夜艳熟免费| 丁香五月网久久综合| 女十八毛片| 两个人视频全免费高清观看| 国产精品深爱在线| 波多野吉衣AV无码| 特级做A爰片毛片免费看| 少妇高潮喷水在线观看| 精品国产乱码久久久久久天狼| 成全影院免费观看电视剧高清| 在线观看伦理片| 日本高清一二三不卡区| 日本熟妇毛茸茸XXXX| 亚洲国产日韩视频观看| 亚洲欧美精品中文字幕| 美女内射毛片在线看3D| 日韩2区| 国产欧美日韩免费| 亚洲一区二区三区高清视频| 国产精品呦呦| 亚洲A∨无码一区二区三区| 欧美又粗又大XXXXBBBB疯狂| 丝袜人妻无码专区视频| 久久久国产麻豆精品一区| 日韩中文字幕在线观看.| 国产欧美视频一区二区三区| 韩国电影理论妈妈的朋友| avtt在线播放| 亚洲AV永久无码天堂网一线| 欧美精品第1页在线播放| 男女高潮又爽又黄又无遮挡| 性XXXXX大片免费视频| 三个男人躁我一个阿啊阿广告| 日本一区午夜艳熟免费|