亚洲中文字幕特级毛片-亚洲制服丝袜中文字幕-亚洲制服丝袜在线观看-亚洲制服欧美自拍另类-免费一级黄色-免费一级国产生活片

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
人妻被按摩师玩弄到潮喷,成人免费视频国产,亚洲中文字幕日产乱码高清app
Rabbit Anti-FOG2/PE-Cy5 Conjugated antibody (bs-11942R-PE-Cy5)
訂購(gòu)熱線:400-901-9800
訂購(gòu)郵箱:sales@www.chomd.com.cn
訂購(gòu)QQ:  400-901-9800
技術(shù)支持:techsupport@www.chomd.com.cn
說(shuō) 明 書: 100ul  
100ul/2980.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-11942R-PE-Cy5
英文名稱 Rabbit Anti-FOG2/PE-Cy5 Conjugated antibody
中文名稱 PE-Cy5標(biāo)記的GATA結(jié)合蛋白2伴侶蛋白抗體
別    名 FOG-2; FOG2_HUMAN; Friend of GATA 2; Friend of GATA protein 2; Friend of GATA2 ; hFOG-2 ; ZFPM2; Zinc finger protein 89B; Zinc finger protein M2; Zinc finger protein multitype 2 ; Zinc finger protein ZFPM2.  
規(guī)格價(jià)格 100ul/2980元 購(gòu)買        大包裝/詢價(jià)
說(shuō) 明 書 100ul  
研究領(lǐng)域 心血管  細(xì)胞生物  神經(jīng)生物學(xué)  信號(hào)轉(zhuǎn)導(dǎo)  轉(zhuǎn)錄調(diào)節(jié)因子  鋅指蛋白  表觀遺傳學(xué)  
抗體來(lái)源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Rabbit, Sheep, )
產(chǎn)品應(yīng)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 128kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human FOG2
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:
The FOG family of transcriptional cofactors, including FOG (friend of GATA-1) and FOG-2, are zinc finger proteins that interact with the GATA family of transcriptional regulators. FOG/GATA-1 complexes are required for erythroid and megakaryocyte maturation, and they promote differentiation during embryonic development. These complexes involve the association between multiple zinc fingers on the FOG proteins and the N-terminal zinc finger of GATA proteins. While FOG cooperatively regulates GATA-1 induced transcription, FOG-2 is able to both positively and negatively influence GATA mediated transcription. FOG-2 is predominantly expressed in heart, neurons and gonads, and it preferentially participates in the regulation of GATA-3, GATA-4 and GATA-6. In cardiomyocytes and fibroblasts, FOG-2 inhibits GATA-4 transcriptional activity, yet FOG-2 restores GATA-1 mediated transcription in erythroid cultures deficient in FOG, suggesting that the observed effects of FOG-2 are context specific and vary between cellular systems.

Function:
Transcription regulator that plays a central role in heart morphogenesis and development of coronary vessels from epicardium, by regulating genes that are essential during cardiogenesis. Essential cofactor that acts via the formation of a heterodimer with transcription factors of the GATA family GATA4, GATA5 and GATA6. Such heterodimer can both activate or repress transcriptional activity, depending on the cell and promoter context. Also required in gonadal differentiation, possibly be regulating expression of SRY. Probably acts a corepressor of NR2F2.

Subunit:
Interacts with the N-terminal zinc-finger of GATA4, GATA5 and probably GATA6. Interacts with retinoid nuclear receptor RXRA when ligand bound (By similarity). Interacts with corepressor CTBP2; this interaction is however not essential for corepressor activity. Able to bind GATA1 in vitro. Interacts with NR2F2 and NR2F6

Subcellular Location:
Nucleus.

Tissue Specificity:
Widely expressed at low level.

DISEASE:
Defects in ZFPM2 may be a cause of tetralogy of Fallot (TOF) [MIM:187500]. TOF is a congenital heart anomaly which consists of pulmonary stenosis, ventricular septal defect, dextroposition of the aorta (aorta is on the right side instead of the left) and hypertrophy of the right ventricle. This condition results in a blue baby at birth due to inadequate oxygenation. Surgical correction is emergent.
Defects in ZFPM2 are the cause of diaphragmatic hernia 3 (DIH3) [MIM:610187]; a form of congenital diaphragmatic hernia (CDH). CDH refers to a group of congenital defects in the structural integrity of the diaphragm associated with often lethal pulmonary hypoplasia and pulmonary hypertension.

Similarity:
Belongs to the FOG (Friend of GATA) family.
Contains 3 C2H2-type zinc fingers.
Contains 5 C2HC-type zinc fingers.

Database links:

Entrez Gene: 23414 Human

Omim: 603693 Human

SwissProt: Q8WW38 Human

Unigene: 431009 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權(quán)所有 2004-2026 www.www.chomd.com.cn 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    證書編號(hào): CQC24QY10047R0M/1100
京ICP備05066980號(hào)-1         京公網(wǎng)安備110107000727號(hào)
主站蜘蛛池模板: 国产成人精品免费久久久久久久久9| 国产无线码高清| 久久人妻少妇嫩草AV蜜桃,欧美亚洲日 | 亚洲一区二区三区91麻豆| 久久精品亚洲综合无码视频免费一区二区三区 | 少妇被黑人到高潮喷出白浆| 91精品国产综合久久精品,亚洲精品国产专区9 | 一区二区网站在线观看无码| 国产在线91在线电影第一页| 天堂8在线天堂资源在线,我的私教老师2在线观看 | 婷婷热久久一个综合| 11一13破女BWXXXX| 国产亚洲精品无码成人网页| 少妇人妻无码精品视频 熟女| 永久亚洲成a人片777777 午夜福利| 国产亚洲精品无码AA在线观看| 色 五月 亚洲 综合 婷婷| 伊人久久96综合| 超碰欧美在线网站页| 精品国产国产综合精品无码国产| 无码在线导航brazzers | 国产一区二区精品久久岳_精品精品国产自在久久 | 成人免费毛片?7?4?7?4?7?4日本片| 久青草国产97香蕉在线视频_| 亚洲国产成人久久综合一品网站| 2021国产麻豆剧传媒 在线| 国产午夜亚洲精品国产,国内精品久 | 色欲Av在线| 亚洲国产午夜精品理论片妓女_久久精品 | 一本色道视频第一页| 被夫上司强迫的女人| 国精品无码一区二区三区D七天 | 久久久久久久999应用下 | 人妻久久久久久| 亚洲h在线播放在线观看H| 一本色道99国产精品蜜挑| 91精品国产乱码久久久久久夜夜嗨 | 亚洲中文字幕久在线,中文字幕无码人妻| 二区三区在线观看视频w| 国内精自视频品线六区免费人 | 波多野结衣一区二区三区av高清十八禁久久 |