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    磷酸化神經(jīng)細(xì)胞分化因子1抗體
    • 產(chǎn)品貨號:
      BN40549R
    • 中文名稱:
      磷酸化神經(jīng)細(xì)胞分化因子1抗體
    • 英文名稱:
      Rabbit anti-phospho-NeuroD1 (Ser274) Polyclonal antibody
    • 品牌:
      Biorigin
    • 貨號

      產(chǎn)品規(guī)格

      售價(jià)

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    • BN40549R-100ul

      100ul

      ¥2470.00

      交叉反應(yīng):Human,Mouse,Rat(predicted:Pig,Cow,Sheep) 推薦應(yīng)用:WB,IHC-P,IHC-F,ICC,IF,ELISA

    產(chǎn)品描述

    英文名稱phospho-NeuroD1 (Ser274)
    中文名稱磷酸化神經(jīng)細(xì)胞分化因子1抗體
    別    名NeuroD1 (phospho S274); p-NeuroD1 (phospho S274); atonal; basic helix loop helix transcription factor; BETA 2; Beta cell E box transactivator 2; BETA2; BHF 1; BHF1; bHLHa3; class A basic helix loop helix protein 3; Class A basic helix-loop-helix protein 3; MODY 6; MODY6; NDF1_HUMAN; NEUROD; NeuroD1; Neurogenic differentiation 1; Neurogenic differentiation factor 1; neurogenic helix loop helix protein NEUROD; NIDDM.  
    產(chǎn)品類型磷酸化抗體 
    研究領(lǐng)域腫瘤  心血管  細(xì)胞生物  神經(jīng)生物學(xué)  表觀遺傳學(xué)  
    抗體來源Rabbit
    克隆類型Polyclonal
    交叉反應(yīng)Human, Mouse, Rat,  (predicted: Pig, Cow, Sheep, )
    產(chǎn)品應(yīng)用WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (石蠟切片需做抗原修復(fù))
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    分 子 量40kDa
    細(xì)胞定位細(xì)胞核 細(xì)胞漿 
    性    狀Liquid
    濃    度1mg/ml
    免 疫 原KLH conjugated Synthesised acetylpeptide derived from human NeuroD1 around the acetylation site of Ser274:PL(p-S)PP 
    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Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
    PubMedPubMed
    產(chǎn)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:
    Differentiation factor required for dendrite morphogenesis and maintenance in the cerebellar cortex. Transcriptional activator. Binds to the insulin gene E-box.

    Subcellular Location:
    Cytoplasm. Nucleus.

    Post-translational modifications:
    Phosphorylated. In islet cells, phosphorylated on Ser-274 upon glucose stimulation; which may be required for nuclear localization. In activated neurons, phosphorylated on Ser-335; which promotes dendritic growth.

    DISEASE:
    Defects in NEUROD1 are the cause of maturity-onset diabetes of the young type 6 (MODY6) [MIM:606394]. MODY is a form of diabetes that is characterized by an autosomal dominant mode of inheritance, onset in childhood or early adulthood (usually before 25 years of age), a primary defect in insulin secretion and frequent insulin-independence at the beginning of the disease.

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

    SWISS:
    Q13562

    Gene ID:
    4760

    Database links:

    Entrez Gene: 4760 Human

    Entrez Gene: 18012 Mouse

    Entrez Gene: 29458 Rat

    Omim: 601724 Human

    SwissProt: Q13562 Human

    SwissProt: Q60867 Mouse

    SwissProt: Q64289 Rat

    Unigene: 574626 Human

    Unigene: 709709 Human

    Unigene: 4636 Mouse

    Unigene: 44289 Rat



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













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