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ADAR1 antibody

https://www.academycancerimmunology.org/web/image/product.template/2138/image_1920?unique=b611535
Volume: 100 µg Purification: Immunogen affinity purified Form: liquid Purity: 95% as determined by SDS-PAGE Host: Rabbit Clonality: polyclonal Clone ID: Isotype: IgG Storage: PBS with 0.02% sodium azide and 50% glycerol pH 7.3,-20? for 12 months(Avoid repeated freeze / thaw cycles.) Background: ADAR1 is also named as ADAR1, DSRAD, G1P1, IFI4. It convert selected adenosine residues into inosine in substrate RNAs containing a relatively short dsRNA region(PMID: 15556947). The human ADAR1 gene specifies two size forms of RNA-specific adenosine deaminase, an interferon(IFN) inducible ?150 kDa protein and a constitutively expressed N-terminally truncated ?110 kDa protein, encoded by transcripts with alternative exon 1 structures that initiate from different promoters(PMID: 11111054). It has 5 isoforms produced by alternative promoter usage and alternative splicing. Defects in ADAR are a cause of dyschromatosis symmetrical hereditaria(DSH).ADAR1 can form respective homodimers, and this association is essential for its enzymatic activities(PMID: 17428802). Immunogen: adenosine deaminase, RNA-specific Synonyms: ADAR, ADAR1, adenosine deaminase, RNA, DRADA, DSH, DSRAD, G1P1, IFI 4, IFI4, Interferon inducible protein 4, K88dsRBP, p136 Observed MW: 110 kDa Uniprot ID: P55265 Reactivity: Human, Mouse, Rat Tested Application: ELISA, IHC, IF, WB, IP Recommended dilution: WB: 1: 500-1: 2000; IHC: 1: 50-1: 200; IP: 1: 200-1: 1000; IF: 1: 20-1: 200 Gene ID: 103 Research Area: Neuroscience, Immunology, Metabolism, Epigenetics

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