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
人人爽久久涩噜噜噜AV,奇米影视7777久久精品人人爽 ,欧美大荫蒂AV高潮
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-GATA1/Cy5 Conjugated antibody (bs-3872R-Cy5)
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-3872R-Cy5
英文名稱1 Rabbit Anti-GATA1/Cy5 Conjugated antibody
中文名稱 Cy5標記的珠蛋白轉(zhuǎn)錄因子1抗體
別    名 GATA1; ERYF 1; ERYF1 antibody Erythroid transcription factor; Erythrold transcription factor 1; GATA 1; GATA binding factor 1; GATA binding protein 1; GF 1; GF1; Globin transcription factor 1; NF E1; NF E1 DNA binding protein; NFE 1; NFE1; GATA1_HUMAN; Erythroid transcription factor; Eryf1; GATA-binding factor 1; GATA-1; GF-1; NF-E1 DNA-binding protein.   
規(guī)格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領(lǐng)域 細胞生物  免疫學(xué)  轉(zhuǎn)錄調(diào)節(jié)因子  細胞表面分子  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, )
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 45kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human GATA1
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:
GATA1 (Globin transcription factor 1) is a Cys2/Cys2 zinc finger DNA binding protein that is expressed primarily in erythroid, megakaryocytic, mast cells and eosinophilic cells. It belongs to the GATA family of transcription factors. GATA1 is a transcriptional activator which probably serves as a general switch factor for erythroid development. It binds to DNA sites with the consensus sequence [AT]GATA[AG] within regulatory regions of globin genes and of other genes expressed in erythroid cells. The protein also plays an important role in erythroid development by regulating the switch from fetal hemoglobin production to adult hemoglobin.

Function:
Transcriptional activator which probably serves as a general switch factor for erythroid development. It binds to DNA sites with the consensus sequence [AT]GATA[AG] within regulatory regions of globin genes and of other genes expressed in erythroid cells.

Subunit:
May form homodimers or heterodimers with other isoforms. Interacts (via the N-terminal zinc finger) with ZFPM1. Interacts with GFI1B. Interacts with PIAS4; the interaction enhances sumoylation and represses the transactivational activity in a sumoylation-independent manner. Interacts with LMCD1.

Subcellular Location:
Nucleus.

Tissue Specificity:
Erythrocytes.

Post-translational modifications:
Highly phosphorylated on serine residues. Phosphorylation on Ser-310 is enhanced on erythroid differentiation. Phosphorylation on Ser-142 promotes sumoylation on Lys-137.
Sumoylation on Lys-137 is enhanced by phosphorylation on Ser-142 and by interaction with PIAS4. Sumoylation by SUMO1 has no effect on transcriptional activity.

DISEASE:
Defects in GATA1 are the cause of X-linked thrombocytopenia with beta-thalassemia (XLTT) [MIM:314050]; also knwon as thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis. XLTT consists of an unusual form of thrombocytopenia with beta-thalassemia. Patients have splenomegaly and petechiae, moderate thrombocytopenia, prolonged bleeding time due to platelet dysfunction, reticulocytosis and unbalanced hemoglobin chain synthesis resembling that of beta-thalassemia minor.
Defects in GATA1 are the cause of anemia without thrombocytopenia X-linked (XLAWT) [MIM:300835]. XLAWT is a form of anemia characterized by abnormal morphology of erythrocytes and granulocytes in peripheral blood, bone marrow dysplasia with hypocellularity of erythroid and granulocytic lineages, and normal or increased number of megakaryocytes. Neutropenia of a variable degree is present in affected individuals.

Similarity:
Contains 2 GATA-type zinc fingers.

Database links:

Entrez Gene: 2623 Human

Entrez Gene: 14460 Mouse

Entrez Gene: 25172 Rat

Omim: 305371 Human

SwissProt: P15976 Human

SwissProt: P17679 Mouse

SwissProt: P43429 Rat

Unigene: 765 Human

Unigene: 335973 Mouse

Unigene: 10024 Rat



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.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
国产片XXXXA片国语对白| 国产精品视频一区二区噜噜| 免费视频网站| 女公务员人妻呻吟求饶| jzzijzzij日本成熟少妇| 国产成人精品三级麻豆| 久久久久久久精品无码AV少妇| 国产乱人伦偷精品视频免下载| 亚洲AV无码国产精品久久不卡 | 差差差很疼30分钟的视频| 中国杭州少妇XXXX做受| 老熟女草BX×| 人妻人人揉人人躁人人A片| av无码在线| 又粗又黄又猛又爽大片免费| 国自产拍偷拍精品啪啪模特| 成人精品视频99在线观看免费| 99精品人妻无码专区在线视频区 | 精品无码AV一区二区三区不卡| 国产后入又长又硬| 亚洲精品~无码抽插| 亚洲AV无码乱码在线观看裸奔| 厨房掀起少妇裙子挺进去| 日本猛少妇色XXXXX猛叫| 宝贝腿开大点我添添公交车| 国产精品99久久久久久人| 荫蒂每天被三个男人添视频 | 麻豆亚洲AV熟女国产一区二| 成人区人妻精品一区二区不卡视频| 欧美日韩人妻精品一区二区三区| 男女做爰爱免费视频A片| 国产精品国产三级国产A| 丁香花在线影院观看在线播放| 精品国产制服丝袜高跟| 欧美激情一区二区三区在线| 国语熟妇乱人乱A片久久| 麻豆AV天堂一二三区视频| 亚洲欧美精品午睡沙发| 色翁荡熄又大又硬又粗又视频| JAPANESEHD熟女熟妇伦| 国产chinasex对白videos麻豆|