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ADAR2 / ADARB1

adenosine deaminase, RNA-specific, B1

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. 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 GRIK2) and serotonin (HTR2C), GABA receptor (GABRA3) and potassium voltage-gated channel (KCNA1). Site-specific RNA editing of transcripts encoding these proteins results in amino acid substitutions which consequently alter their functional activities. Edits GRIA2 at both the Q/R and R/G sites efficiently but converts the adenosine in hotspot1 much less efficiently. Can exert a proviral effect towards human immunodeficiency virus type 1 (HIV-1) and enhances its replication via both an editing-dependent and editing-independent mechanism. The former involves editing of adenosines in the 5'UTR while the latter occurs via suppression of EIF2AK2/PKR activation and function. Can inhibit cell proliferation and migration and can stimulate exocytosis.

Gene Name: adenosine deaminase, RNA-specific, B1
Synonyms: ADARB1, ADAR2a-L3, ADAR2, ADAR2g, ADAR2a, ADAR2a-L2, ADAR2d, DsRNA adenosine deaminase, DRABA2, DRADA2, ADAR2a-L1, ADAR2b, ADAR2c, HRED1, RED1, RNA editase, RED1 homolog, RNA editing deaminase 1, RNA-editing deaminase 1, RNA-editing enzyme 1
Target Sequences: NM_001112 NP_001103.1 P78563

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Products
Proteins (10)
Over-Expression Lysate (6)
Recombinant (4)
ADAR2 / ADARB1 (10)
No (10)
GST (1)
GST, N-terminus (1)
Myc-DDK (Flag) (8)
Human (7)
293T Cells (3)
HEK 293 Cells (5)
Wheat Germ Extract (2)
Purified (1)
ADAR2 / ADARB1 Protein - 12.5% SDS-PAGE Stained with Coomassie Blue.
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Wheat Germ Extract
GST, N-terminus
10 µg/$479; 25 µg/$670
ADAR2 / ADARB1 Protein - Purified recombinant protein ADARB1 was analyzed by SDS-PAGE gel and Coomassie Blue Staining
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HEK 293 Cells
Myc-DDK (Flag)
76.5 kDa
20 µg/$1,107
ADAR2 / ADARB1 Protein - Western validation with an anti-DDK antibody * L: Control HEK293 lysate R: Over-expression lysate
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HEK 293 Cells
Myc-DDK (Flag)
80.6 kDa
100 µg/$710
ADAR2 / ADARB1 Protein - 12.5% SDS-PAGE of human ADARB1 stained with Coomassie Blue
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Wheat Germ Extract
GST
107.2 kDa
2 µg/$439
ADAR2 / ADARB1 Protein - Western validation with an anti-DDK antibody * L: Control HEK293 lysate R: Over-expression lysate
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293T Cells
Myc-DDK (Flag)
76.5 kDa
20 µg/$150
ADAR2 / ADARB1 Protein - Western validation with an anti-DDK antibody * L: Control HEK293 lysate R: Over-expression lysate
Select
293T Cells
Myc-DDK (Flag)
80.6 kDa
20 µg/$215
ADAR2 / ADARB1 Protein - Western validation with an anti-DDK antibody * L: Control HEK293 lysate R: Over-expression lysate
Select
293T Cells
Myc-DDK (Flag)
73.5 kDa
20 µg/$215
ADAR2 / ADARB1 Protein - Purified recombinant protein ADARB1 was analyzed by SDS-PAGE gel and Coomassie Blue Staining
Select
HEK 293 Cells
Myc-DDK (Flag)
80.6 kDa
20 µg/$1,107
ADAR2 / ADARB1 Protein - Western validation with an anti-DDK antibody * L: Control HEK293 lysate R: Over-expression lysate
Select
HEK 293 Cells
Myc-DDK (Flag)
73.5 kDa
100 µg/$710
ADAR2 / ADARB1 Protein - Western validation with an anti-DDK antibody * L: Control HEK293 lysate R: Over-expression lysate
Select
HEK 293 Cells
Myc-DDK (Flag)
76.5 kDa
100 µg/$494
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For RESEARCH USE ONLY. Intended for use by laboratory professionals. Not intended for human diagnostic or therapeutic purposes.

The data on this page has been compiled from LifeSpan internal sources, the National Center for Biotechnology Information (NCBI), and The Universal Protein Resource (UniProt).