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          • Primary Antibodies ›
          • ADAR1 Antibodies

          Invitrogen

          ADAR Polyclonal Antibody

          View all (23) ADAR1 antibodies

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          Cite ADAR Polyclonal Antibody

          Additional Information:
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          • Antibody Testing Data (1)
          ADAR Antibody in Immunohistochemistry (Paraffin) (IHC (P))
          Group 53 Created with Sketch.
          ADAR Antibody in Immunohistochemistry (Paraffin) (IHC (P))
          Group 53 Created with Sketch.

          FIGURE: 1 / 1

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          ADAR Antibody (PA5-49815) in IHC (P)

          Immunohistochemical analysis of ADAR in paraffin-embedded Human brain tissue using ADAR Polyclonal Antibody (Product # PA5-49815). {{ $ctrl.currentElement.advancedVerification.fullName }} validation info. View more
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          ADAR Antibody in Immunohistochemistry (Paraffin) (IHC (P))
          ADAR Polyclonal Antibody

          Product Details

          PA5-49815

          Applications
          Tested Dilution
          Publications

          Immunohistochemistry (Paraffin) (IHC (P))

          1:50-1:100
          -
          Product Specifications

          Species Reactivity

          Human, Mouse

          Host/Isotype

          Rabbit / IgG

          Class

          Polyclonal

          Type

          Antibody

          Immunogen

          Synthesized peptide derived from C-terminal of human ADAR1.
          3D Epitope / Immunogen

          Conjugate

          Unconjugated Unconjugated Unconjugated

          Form

          Liquid

          Concentration

          1 mg/mL

          Amount

          100 µg

          Purification

          Antigen affinity chromatography

          Storage buffer

          PBS, pH 7.4, with 50% glycerol

          Contains

          0.02% sodium azide

          Storage conditions

          -20°C

          Shipping conditions

          Ambient (domestic); Wet ice (international)

          RRID

          AB_2635268

          Product Specific Information

          The antibody detects endogenous levels of total ADAR protein.

          Target Information

          Adenosine Deaminase RNA Specific (ADAR) catalyzes the hydrolytic deamination of adenosine to inosine in double-stranded RNA (dsRNA) referred to as A-to-I RNA editing.This may affect gene expression and function in a number of ways that include mRNA translation by changing codons and hence the amino acid sequence of proteins; pre-mRNA splicing by altering splice site recognition sequences; RNA stability by changing sequences involved in nuclease recognition; genetic stability in the case of RNA virus genomes by changing sequences during viral RNA replication; and RNA structure-dependent activities such as microRNA production or targeting or protein-RNA interactions. ADAR can edit both viral and cellular RNAs and can edit RNAs at multiple sites (hyper-editing) or at specific sites (site-specific editing). Its cellular RNA substrates include: bladder cancer-associated protein (BLCAP), neurotransmitter receptors for glutamate (GRIA2) and serotonin (HTR2C) and GABA receptor (GABRA3). Site-specific RNA editing of transcripts encoding these proteins results in amino acid substitutions which consequently alters their functional activities. Exhibits low-level editing at the GRIA2 Q/R site, but edits efficiently at the R/G site and HOTSPOT1. Its viral RNA substrates include: hepatitis C virus (HCV), vesicular stomatitis virus (VSV), measles virus (MV), hepatitis delta virus (HDV), and human immunodeficiency virus type 1 (HIV-1). Exhibits either a proviral (HDV, MV, VSV and HIV-1) or an antiviral effect (HCV) and this can be editing-dependent (HDV and HCV), editing-independent (VSV and MV) or both (HIV-1). Impairs HCV replication via RNA editing at multiple sites. Enhances the replication of MV, VSV and HIV-1 through an editing-independent mechanism via suppression of EIF2AK2/PKR activation and function. Stimulates both the release and infectivity of HIV-1 viral particles by an editing-dependent mechanism where it associates with viral RNAs and edits adenosines in the 5'UTR and the Rev and Tat coding sequence. Can enhance viral replication of HDV via A-to-I editing at a site designated as amber/W, thereby changing an UAG amber stop codon to an UIG tryptophan (W) codon that permits synthesis of the large delta antigen (L-HDAg) which has a key role in the assembly of viral particles. However, high levels of ADAR1 inhibit HDV replication. (Uniprot)

          For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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          Cite this product

          Bioinformatics

          Protein Aliases: 136 kDa double-stranded RNA-binding protein; ADA; ADAR1; Adenosine Deaminase; adenosine deaminase acting on RNA 1-A; Double-stranded RNA-specific adenosine deaminase; DRADA; dsRNA adenosine deaminase; dsRNA adeonosine deaminase; IFI-4; interferon-induced protein 4; Interferon-inducible protein 4; K88DSRBP; p136; RNA adenosine deaminase 1; RNA-specific adenosine deaminase p110 form; RNA-specific adenosine deaminase p150 form; unnamed protein product

          View more View less

          Gene Aliases: ADAR; ADAR1; Adar1p110; Adar1p150; AGS6; AV242451; DRADA; DSH; DSRAD; G1P1; IFI-4; IFI4; K88DSRBP; mZaADAR; P136

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          UniProt ID: (Human) P55265, (Mouse) Q99MU3

          View more View less

          Entrez Gene ID: (Human) 103, (Mouse) 56417

          View more View less

          Function(s)
          DNA binding RNA binding double-stranded RNA binding double-stranded RNA adenosine deaminase activity adenosine deaminase activity protein binding tRNA-specific adenosine deaminase activity hydrolase activity metal ion binding left-handed Z-DNA binding poly(A) RNA binding RNA metabolism protein nucleic acid metabolism protein
          Process(es)
          osteoblast differentiation hematopoietic progenitor cell differentiation immune system process somatic diversification of immune receptors via somatic mutation adenosine to inosine editing RNA processing mRNA processing protein import into nucleus protein export from nucleus apoptotic process response to virus base conversion or substitution editing erythrocyte differentiation gene silencing by RNA pre-miRNA processing production of miRNAs involved in gene silencing by miRNA response to interferon-alpha negative regulation of protein kinase activity by regulation of protein phosphorylation positive regulation of viral genome replication innate immune response defense response to virus definitive hemopoiesis negative regulation of type I interferon-mediated signaling pathway hematopoietic stem cell homeostasis small RNA loading onto RISC hepatocyte apoptotic process cellular response to virus negative regulation of RNA interference negative regulation of hepatocyte apoptotic process in utero embryonic development transcription, DNA-templated regulation of transcription, DNA-templated miRNA loading onto RISC involved in gene silencing by miRNA negative regulation of apoptotic process negative regulation of viral genome replication
          It has to be done as per old AB suggested Products section.

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