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    2. 最近搜索:細胞培養 微生物學 分子生物 生物化學
      首頁>>免疫學>>一抗>>雙鏈RNA腺苷酸脫氨基酶抗體(C端)
      雙鏈RNA腺苷酸脫氨基酶抗體(C端)
      • 產品貨號:
        BN40669R
      • 中文名稱:
        雙鏈RNA腺苷酸脫氨基酶抗體(C端)
      • 英文名稱:
        Rabbit anti-ADAR1 Polyclonal antibody
      • 品牌:
        Biorigin
      • 貨號

        產品規格

        售價

        備注

      • BN40669R-100ul

        100ul

        ¥2360.00

        交叉反應:Human,Mouse,Rat 推薦應用:WB,IHC-P,IHC-F,IF,ELISA

      • BN40669R-200ul

        200ul

        ¥3490.00

        交叉反應:Human,Mouse,Rat 推薦應用:WB,IHC-P,IHC-F,IF,ELISA

      產品描述

      英文名稱ADAR1
      中文名稱雙鏈RNA腺苷酸脫氨基酶抗體(C端)
      別    名136kDa double stranded RNA binding protein; Adar 1; ADAR; Adar1; Adenosine deaminase RNA specific 1; Adenosine deaminase RNA specific; Adenosine deaminase that act on RNA; AV242451; Double stranded RNA specific adenosine deaminase; Double-stranded RNA-specific editase Adar; Drada; Dsh; Dsrad; dsRNA adenosine deaminase; EC 3.5.4.-; G1P1; IFI 4; IFI4; Ifi4 protein; Interferon induced protein 4; Interferon inducible protein 4; K88dsrbp; mZaADAR; p136; Pre-mRNA adenosine deaminase; RNA adenosine deaminase 1; RNA-editing deaminase 1; RNA-editing enzyme 1.  
      研究領域細胞生物  免疫學  細胞周期蛋白  
      抗體來源Rabbit
      克隆類型Polyclonal
      交叉反應Human, Mouse, Rat, 
      產品應用WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 (石蠟切片需做抗原修復)
      not yet tested in other applications.
      optimal dilutions/concentrations should be determined by the end user.
      分 子 量135kDa
      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 DRADA:1001-1226/1226 
      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
      產品介紹This gene encodes the enzyme responsible for RNA editing by site-specific deamination of adenosines. This enzyme destabilizes double-stranded RNA through conversion of adenosine to inosine. Mutations in this gene have been associated with dyschromatosis symmetrica hereditaria. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2010]

      Function:
      Converts multiple adenosines to inosines and creates I/U mismatched base pairs in double-helical RNA substrates without apparent sequence specificity. Has been found to modify more frequently adenosines in AU-rich regions, probably due to the relative ease of melting A/U base pairs as compared to G/C pairs. Functions to modify viral RNA genomes and may be responsible for hypermutation of certain negative-stranded viruses. Edits the messenger RNAs for glutamate receptor (GLUR) subunits by site-selective adenosine deamination. Produces low-level editing at the GLUR-B Q/R site, but edits efficiently at the R/G site and HOTSPOT1. Binds to short interfering RNAs (siRNA) without editing them and suppresses siRNA-mediated RNA interference. Binds to ILF3/NF90 and up-regulates ILF3-mediated gene expression.

      Subunit:
      Homodimer. Isoform 1 interacts with ILF2/NF45 and ILF3/NF90.

      Subcellular Location:
      Cytoplasm. Nucleus, nucleolus. Isoform 1: Cytoplasm. Note=Found predominantly in cytoplasm but appears to shuttle between the cytoplasm and nucleus. Isoform 5: Nucleus, nucleolus.

      Tissue Specificity:
      Ubiquitously expressed, highest levels were found in brain and lung.

      Post-translational modifications:
      Sumoylation reduces RNA-editing activity.

      DISEASE:
      Defects in ADAR are a cause of dyschromatosis symmetrical hereditaria (DSH) [MIM:127400]; also known as reticulate acropigmentation of Dohi. DSH is a pigmentary genodermatosis of autosomal dominant inheritance characterized by a mixture of hyperpigmented and hypopigmented macules distributed on the dorsal parts of the hands and feet.

      Similarity:
      Contains 1 A to I editase domain.
      Contains 2 DRADA repeats.
      Contains 3 DRBM (double-stranded RNA-binding) domains.

      SWISS:
      P55265

      Gene ID:
      103

      Database links:

      Entrez Gene: 103 Human

      Entrez Gene: 56417 Mouse

      Omim: 146920 Human

      SwissProt: P55265 Human

      SwissProt: Q99MU3 Mouse

      Unigene: 12341 Human

      Unigene: 679967 Human

      Unigene: 316628 Mouse



      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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