mm1313亚洲精品,欧美俄罗斯40老熟妇,欧美日韩在线观看视频在线,亚洲欧美国产激情综合在线

掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  關于我們  聯(lián)系我們
一级做a爰片欧美aaaa片,aaa国产精品一区二区
首頁 > 產(chǎn)品中心 > 標記一抗 > 產(chǎn)品信息
Rabbit Anti-GATA1/BF350 Conjugated antibody (bs-3872R-BF350)
訂購熱線:400-901-9800
訂購郵箱:sales@m.p2b3.cn
訂購QQ:  400-901-9800
技術支持:techsupport@m.p2b3.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產(chǎn)品編號 bs-3872R-BF350
英文名稱 Rabbit Anti-GATA1/BF350 Conjugated antibody
中文名稱 BF350標記的珠蛋白轉錄因子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  
研究領域 細胞生物  免疫學  轉錄調節(jié)因子  細胞表面分子  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, )
產(chǎn)品應用 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.
版權所有 2004-2026 www.m.p2b3.cn 北京博奧森生物技術有限公司
通過國際質量管理體系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
69国产成人综合久久精| 国产精品久久久久妇| 黑人插中国女人逼| 鸡巴插骚逼真舒服| 亚洲国产精品一区亚洲国产| 少妇毛片一区二区三区免费视频| 日韩精品欧美喷水| 高颜值情侣鸡巴插插淫叫| 中文字幕乱码人妻一区二区三区| 加勒比五月综合久久伊人| 国产 欧美 日韩 黄片| 最是人间烟火色在线播放| 猛插女人小穴视频| 美女大鸡操很多水在线看| 久久一级高潮a免费| 精品无码国产一区二区三区A| 男人草女人的视频免费看| 国产合区在线一区二区三区| 青青视频在线人视频在线| 黑人猛操日本美女| 美女亚洲福利视频| 又色又爽又黄的吃奶Av| 精品无码国产一区二区三区麻豆| 高颜值美女视频在线观看| 美女的粉嫩小逼视频特写| 欧美国产日韩a欧美在线| 九九在线精品亚洲国产| 白虎美女被大基吧操| 被几个大屌老外轮操| 无码人妻丰满熟妇区精品| 最新的亚洲欧美中文字幕| 欧美一区二区高清视频在线观看| 伊人久久丁香色婷婷啪啪| 泰国无码AV片在线观看| 性色av少妇一区二区三区多人| 国产一国产一级毛片无码视频百度| 日韩无码av三级片| 午夜性刺激在线视频免费| 爽妇网国产精品24| 成人精品视频区一区二区三| 久久久中文字幕在线视频|