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
久久久久久不卡国产精品,亚洲精品一二三区av,欧美亚洲尤物99精品
首頁 > 產品中心 > 一抗 > 產品信息
NEUROD1, BF750 conjugated (bs-1517R-BF750)  
訂購熱線:400-901-9800
訂購郵箱:sales@www.p2b3.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.p2b3.cn
100ul/2980.00元
大包裝/詢價
產品編號 bs-1517R-BF750
英文名稱 NEUROD1, BF750 conjugated
中文名稱 BF750標記的神經細胞分化因子1抗體
別    名 atonal; Neurod1 protein; basic helix loop helix transcription factor; bHLHa3; class A basic helix loop helix protein 3; Class A basic helix-loop-helix protein 3; MODY 6; MODY6; NDF1_HUMAN; NeuroD1; neurogenic helix loop helix protein NEUROD; Beta cell E box transactivator 2; BETA2; BHF 1; BHF1; NEUROD; Neurogenic differentiation 1; Neurogenic differentiation factor 1; NIDDM; BHLHA3.  
研究領域 腫瘤  心血管  免疫學  染色質和核信號  神經生物學  干細胞  新陳代謝  表觀遺傳學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應
產品應用
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 40kDa
細胞定位 細胞核 細胞漿 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human NEUROD1: 21-120/356 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 This gene encodes a member of the NeuroD family of basic helix-loop-helix (bHLH) transcription factors. The protein forms heterodimers with other bHLH proteins and activates transcription of genes that contain a specific DNA sequence known as the E-box. It regulates expression of the insulin gene, and mutations in this gene result in type II diabetes mellitus. [provided by RefSeq, Jul 2008]

Function:
Acts as a transcriptional activator: mediatestranscriptional activation by binding to E box-containing promoterconsensus core sequences 5'-CANNTG-3'. Associates with the p300/CBPtranscription coactivator complex to stimulate transcription of thesecretin gene as well as the gene encoding the cyclin-dependentkinase inhibitor CDKN1A. Contributes to the regulation of severalcell differentiation pathways, like those that promote theformation of early retinal ganglion cells, inner ear sensoryneurons, granule cells forming either the cerebellum or the dentategyrus cell layer of the hippocampus, endocrine islet cells of thepancreas and enteroendocrine cells of the small intestine. Togetherwith PAX6 or SIX3, is required for the regulation of amacrine cellfate specification. Also required for dendrite morphogenesis andmaintenance in the cerebellar cortex. Associates with chromatin toenhancer regulatory elements in genes encoding key transcriptionalregulators of neurogenesis (By similarity).

Subunit:
Interacts (via helix-loop-helix motif domain) with EP300(via C-terminus) (By similarity). Heterodimer with TCF3/E47; theheterodimer is inhibited in presence of ID2, but not NR0B2, toE-box element. Efficient DNA-binding requires dimerization withanother bHLH protein. Interacts with RREB1. Interacts with EP300;the interaction is inhibited by NR0B2. Interacts with TCF3; theinteraction is inhibited by ID2.

Subcellular Location:
Cytoplasm. Nucleus. Note=Inpancreatic islet cells, shuttles to the nucleus in response toglucose stimulation. Colocalizes with NR0B2 in thenucleus.

Post-translational modifications:
Phosphorylated. In islet cells, phosphorylated on Ser-274upon glucose stimulation; which may be required for nuclearlocalization. In activated neurons, phosphorylated on Ser-335;which promotes dendritic growth. Phosphorylated by MAPK1;phosphorylation regulates heterodimerization and DNA-bindingactivities. Phosphorylation on Ser-266 and Ser-274 increasestransactivation on the insulin promoter in glucose-stimulatedinsulinoma cells (By similarity).

DISEASE:
Maturity-onset diabetes of the young 6 (MODY6)[MIM:606394]: A form of diabetes that is characterized by anautosomal dominant mode of inheritance, onset in childhood or earlyadulthood (usually before 25 years of age), a primary defect ininsulin secretion and frequent insulin-independence at thebeginning of the disease. Note=The disease is caused by mutationsaffecting the gene represented in this entry.

Similarity:
Contains 1 bHLH (basic helix-loop-helix) domain.

SWISS:
Q13562

Gene ID:
4760

版權所有 2004-2026 www.www.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         京公網安備110107000727號
欧美高清在线观看一区二区三区| 黄色片视频1024| 女同舔我下面直流水| 日韩人妻精品一区二区三区99| 日本黑鸡吧黄色录像| 黑丝美女被操到高潮| 日本高清一区二区三区水蜜桃| 熟妇女人妻丰满中文字幕| 欧美99热这里都是精品| 久久久国产调教性奴| 狠狠色伊人亚洲综合成人| 骚穴 操我 视频| 欧美成人精品一区二区免费看| a一级毛片免费高清在线| 久久综合色鬼综合色| 被几个大屌老外轮操| 神马我不卡手机在线观看| 黑人大鸡把操逼视频| 国产精品亚洲一区二区三区极品| 亚洲精品成人无码app| 精品少妇一区二区三区中文字幕| 亚洲AV无码一区二区三区系列| 大黑屌狂操骚逼视频| 欧美性一区二区三区五区| 免费骚逼潮吹av| 中文字幕乱码人妻一区二区三区| 日韩人妻精品一区二区三区| 国产午夜精品美女视频露脸| 欧美一区二区三区高清性群p| 亚洲高清无遮挡在线观看| 大波美女被插的好爽| 大阴茎交于大阴户黄片视频| 久久精精品久久久久噜噜| 骚女人被大吊干视‘| 中文字幕乱码人妻一区二区三区| 中文有码无码人妻在线看| 欧美另类在线观看| 欧美大鸡巴操大骚逼| 日本欧美一区二区三区| 三级无码日B视频| 亚洲成国产人片在线观看|