吃奶呻吟打开双腿做受动态图 -亚洲色偷偷色噜噜狠狠99网-日韩精品极品视频在线观看免费-来一水AV@lysav

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  人才招聘  關(guān)于我們  聯(lián)系我們
99久久精品日本一区二区免费,欧美一区二区三区成人片在线,国产在线国偷精品免费看
Rabbit Anti-GATA6/BF488 Conjugated antibody (bs-1787R-BF488)
訂購熱線:400-901-9800
訂購郵箱:sales@xucheq.com
訂購QQ:  400-901-9800
技術(shù)支持:techsupport@xucheq.com
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-1787R-BF488
英文名稱1 Rabbit Anti-GATA6/BF488 Conjugated antibody
中文名稱 BF488標(biāo)記的GATA結(jié)合蛋白6抗體
別    名 Gata binding factor 6; Gata binding protein 6; GATA-binding factor 6; Gata6; GATA6_HUMAN; Transcription factor Gata 6; Transcription factor GATA-6.  
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  心血管  細(xì)胞生物  免疫學(xué)  發(fā)育生物學(xué)  染色質(zhì)和核信號  干細(xì)胞  轉(zhuǎn)錄調(diào)節(jié)因子  結(jié)合蛋白  表觀遺傳學(xué)  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) Human,  (predicted: Mouse, Rat, Chicken, Dog, Pig, Cow, 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 60kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human GATA-6
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:
This gene is a member of a small family of zinc finger transcription factors that play an important role in the regulation of cellular differentiation and organogenesis during vertebrate development. This gene is expressed during early embryogenesis and localizes to endo- and mesodermally derived cells during later embryogenesis and thereby plays an important role in gut, lung, and heart development. Mutations in this gene are associated with several congenital defects. [provided by RefSeq, Mar 2012].

Function:
Transcriptional activator that regulates SEMA3C and PLXNA2. Thought to be important for regulating terminal differentiation and/or proliferation.

Subunit:
Interacts with LMCD1 (By similarity).

Subcellular Location:
Nucleus.

Tissue Specificity:
Expressed in heart, gut and gut-derived tissues.

DISEASE:
Defects in GATA6 are a cause of conotruncal heart malformations (CTHM) [MIM:217095]. A group of congenital heart defects involving the outflow tracts. Examples include truncus arteriosus communis, double-outlet right ventricle and transposition of great arteries. Truncus arteriosus communis is characterized by a single outflow tract instead of a separate aorta and pulmonary artery. In transposition of the great arteries, the aorta arises from the right ventricle and the pulmonary artery from the left ventricle. In double outlet of the right ventricle, both the pulmonary artery and aorta arise from the right ventricle. Note=GATA6 mutations have been found in patients with non-syndromic persistent truncus arteriosus (PubMed:19666519).
Defects in GATA6 are the cause of atrial septal defect type 9 (ASD9) [MIM:614475]. A congenital heart malformation characterized by incomplete closure of the wall between the atria resulting in blood flow from the left to the right atria. Some patients manifest tricuspid valve disease, pulmonary valve disease, and pulmonary artery hypertension.
Defects in GATA6 are a cause of tetralogy of Fallot (TOF) [MIM:187500]. 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. In this condition, blood from both ventricles (oxygen-rich and oxygen-poor) is pumped into the body often causing cyanosis.
Defects in GATA6 are the cause of atrioventricular septal defect type 5 (AVSD5) [MIM:614474]. A congenital heart malformation characterized by a common atrioventricular junction coexisting with deficient atrioventricular septation. The complete form involves underdevelopment of the lower part of the atrial septum and the upper part of the ventricular septum; the valve itself is also shared. A less severe form, known as ostium primum atrial septal defect, is characterized by separate atrioventricular valvar orifices despite a common junction.
Defects in GATA6 are a cause of pancreatic agenesis and congenital heart defects (PACHD) [MIM:600001]. An autosomal dominant disease characterized by pancreatic severe hypoplasia or agenesis, diabetes mellitus, and congenital heart abonormalities including ventricular septal defect, patent ductus arteriosus, pulmonary artery stenosis, truncus arteriosus and tetralogy of Fallot.

Similarity:
Contains 2 GATA-type zinc fingers.

Database links:

Entrez Gene: 2627 Human

Entrez Gene: 14465 Mouse

Entrez Gene: 29300 Rat

Omim: 601656 Human

SwissProt: Q92908 Human

SwissProt: Q61169 Mouse

SwissProt: P46153 Rat

Unigene: 514746 Human

Unigene: 329287 Mouse

Unigene: 8701 Rat



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

GATA6又稱轉(zhuǎn)錄調(diào)節(jié)因子GATA6,可能抑制Wnt路徑,方式是通過直接調(diào)控Wnt路徑中另一種名為Fzd2的蛋白的表達(dá)。而Wnt路徑是干細(xì)胞生物學(xué)中一個主要的路徑。GATA6負(fù)調(diào)控Wnt路徑并且其已被證明在胚胎干細(xì)胞復(fù)制和分化中也起重要作用。
版權(quán)所有 2004-2026 www.xucheq.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
免费A片国产毛无码A片| 无码人妻精品一区二区三区东京热| 无码H黄肉3D动漫在线观看| 高清毛片AAAAAAAAA片| 国产精品丝袜久久久久久不卡| 奇米影视777| 欧美黑人粗暴多交高潮水最多| 国产精品永久免费视频| 人妻无码| 艳妇乳肉豪妇荡乳| 国产精品宾馆在线精品酒店| 国产精品无码AV无码| 日韩精品无码中文字幕一区二区| 隔着内裤揉搓她的花蒂H漫画| 欧美激情第1页| 99久久99久久免费精品小说| 少妇高潮惨叫久久久久久| 97精品国产手机| 亚洲熟妇无码另类久久久| 亚洲国产精华液网站w| 国产成人无码综合亚洲日韩 | 精品无码人妻一区二区三区| 成人自慰女黄网站免费大全| 国产成人一区二区三区| 99精品一区二区三区无码吞精 | 久久99国产精一区二区三区| 妈妈的朋友2在线观看| 久久国产精品-国产精品| 成人区色情综合小说| 下面一进一出好爽视频| 美女露出奶头扒开尿口| 久久久综合香蕉尹人综合网| 男男暴菊GAY无套网站| 国产精品18久久久久久VR| 成人综合婷婷国产精品久久蜜臀| 1000部精品久久久久久久久| 国产偷窥熟妇高潮呻吟| 波多野结AV衣东京热无码专区| 国产亚洲成AV人片在线观黄桃| 三上悠亚SSⅠN939无码播放| 亚洲乱码日产精品BD在线观看|