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雙鏈RNA腺苷酸脫氨基酶抗體(C端)

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雙鏈RNA腺苷酸脫氨基酶抗體(C端)
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雙鏈RNA腺苷酸脫氨基酶抗體(C端)()

英文名稱: Anti-ADAR1 (C-terminus)                                  濃度: 1mg/1ml 

抗體來源:Rabbit

克隆類型:polyclonal          

 交叉反應(yīng):    Human, Mouse, Rat,   

產(chǎn)品類型: 一抗  

性    狀:Lyophilized or Liquid 

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 :ADAR1 converts adenosine to inosine in dsRNA, which destabilizes the dsRNA helix. This activity is important for various functions like site-specific RNA editing of transcripts of the glutamate receptors and modifying viral RNA genomes (which may be responsible for hypermutation of certain negative-stranded viruses, e.g., measles virus). ADAR1 also binds to short interfering RNAs (siRNA) without editing them and suppresses siRNA-mediated RNA interference. This protein is ubiquitously expressed, with the highest levels being found in brain and lung.

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.

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