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(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  關(guān)于我們  聯(lián)系我們
日本视频一区二区二三区,国产成年无码久久久久毛片,av一区二区三区在线看
Rabbit Anti-GATA1/Cy5 Conjugated antibody (bs-3872R-Cy5)
訂購熱線:400-901-9800
訂購郵箱:sales@m.p2b3.cn
訂購QQ:  400-901-9800
技術(shù)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-Cy5
英文名稱 Rabbit Anti-GATA1/Cy5 Conjugated antibody
中文名稱 Cy5標(biāo)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(xì)胞生物  免疫學(xué)  轉(zhuǎn)錄調(diào)節(jié)因子  細(xì)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.m.p2b3.cn 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
一区二区三区四区五六区| 黑丝美女被操到高潮| 久久精品人人爽人人爽快| 大鸡巴插入骚穴在线观看| 欧美十八一区二区三区| 骚逼被操视频拳交| 农村胖肥胖女人操逼视频| 午夜精品福利一区二区三区蜜桃p| 欧美日韩一区精品一区精品| 韩国年轻的母亲在线观看| 国产免费好大好硬| 中文字幕在线观一二三区| 精品国产Av无码久久久一区二区| 五月天国产成人av在线| 久久久精品欧美一区二区三免费| 日本美女阴户射尿| 日韩aaa成人免费观看| 中文字幕在线观看第二页| 欧美精品国产一区二区在线观看| 男生的小鸡鸡插进女生的桃子 里| 91精品国产剧情欧美一区二区| 操纯欲女生小穴视频| 波多野吉衣吹潮Av| 大鸡吧干小逼逼视频大全| 久久精品欧美精品免费观看| 日韩欧美一级特黄大片欧| 熟妇人妻无乱码中文字幕| 偷窥国内肥臀老熟女视频| 日韩高清毛片在线观看| 欧美精品视频在线| 欧美性爱撅臀插入啪啪啪| 可以免费看污污片的软件| 久久久久久国产A免费观看| 国产成人精品区在线观看| 日本一区二区高清免费不卡| 狠狠五月激情综合去干网| 美女被插b在线观看| 精华欧美一区二区久久久| 国产欧美亚洲一区二区三| 国产精选三级在线观看| 无码人妻免费一区二区三区|