ADAR Primary Antibody

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Description
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.
Product Overview
Formulation
Purified antibody in PBS with 0.05% sodium azide
Storage
4°C; -20°C for long term storage
Product Image
Elisa
Figure 1: Black line: Control Antigen (100 ng);Purple line: Antigen (10ng); Blue line: Antigen (50 ng); Red line:Antigen (100 ng)
Figure 1: Black line: Control Antigen (100 ng);Purple line: Antigen (10ng); Blue line: Antigen (50 ng); Red line:Antigen (100 ng)
Western Blot
Figure 2:Western blot analysis using ADAR mAb against human ADAR (AA: 1085-1223) recombinant protein. (Expected MW is 42.1 kDa)
Figure 2:Western blot analysis using ADAR mAb against human ADAR (AA: 1085-1223) recombinant protein. (Expected MW is 42.1 kDa)
Western Blot
Figure 3:Western blot analysis using ADAR mAb against HEK293 (1) and ADAR (AA: 1085-1223)-hIgGFc transfected HEK293 (2) cell lysate.
Figure 3:Western blot analysis using ADAR mAb against HEK293 (1) and ADAR (AA: 1085-1223)-hIgGFc transfected HEK293 (2) cell lysate.
Western Blot
Figure 4:Western blot analysis using ADAR mouse mAb against Ramos (1), K562 (2), and Jurkat (3) cell lysate.
Figure 4:Western blot analysis using ADAR mouse mAb against Ramos (1), K562 (2), and Jurkat (3) cell lysate.
Flow cytometric
Figure 5:Flow cytometric analysis of HeLa cells using ADAR mouse mAb (green) and negative control (red).
Figure 5:Flow cytometric analysis of HeLa cells using ADAR mouse mAb (green) and negative control (red).
For Research Use Only. Not for use in diagnostic procedures.