

| 货号 | ARO-A13907 |
|---|---|
| 品牌 | ProteoGenix |
| 描述 |
Anti-ADAR/IFI4 Polyclonal Antibody (ARO-A13907) is a rabbit polyclonal antibody detecting Double-stranded RNA-specific adenosine deaminase, G1P1, IFI-4, ADAR, K88DSRBP, DRADA, ADAR1, IFI4, Interferon-inducible protein 4, p136, 136 kDa double-stranded RNA-binding protein, DSRAD in ELISA, IHC, WB. Suitable for Human, Rat.
Highlights
|
| 种属反应性 | Human, Rat |
| 应用 | ELISA, IHC, WB |
| 宿主 | Rabbit |
| 同种型 | IgG |
| 克隆类型 | Polyclonal |
| 免疫原 | E. coli - derived recombinant Human ADAR/IFI4 (Asn503-Val885). |
| 靶标 | Double-stranded RNA-specific adenosine deaminase, G1P1, IFI-4, ADAR, K88DSRBP, DRADA, ADAR1, IFI4, Interferon-inducible protein 4, p136, 136 kDa double-stranded RNA-binding protein, DSRAD |
| 纯化方式 | Purified by antigen affinity column. |
| Accession号 | P55265 |
| 状态 | Liquid |
| 保存溶液 | 0.01M PBS, pH 7.4, 50% Glycerol, 0.05% Proclin 300. Please refer to the specific buffer information in the hardcopy of datasheet or the lot-specific COA. |
| 稳定性和存储 | Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt. |
| 背景 | Double-stranded RNA-specific adenosine deaminase (ADAR/IFI4) is a ~136 kDa protein. 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 since the translational machinery read the inosine as a guanosine; 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 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. 1. Cho, DS. et al. (2003) The Journal of biological chemistry 278, 17093-102. PMID: 12618436 2. Patterson, JB. et al. (1995) Molecular and cellular biology 15, 5376-88. PMID: 7565688 3. Kim, U. et al. (1994) Proceedings of the National Academy of Sciences of the United States of America 91, 11457-61. PMID: 7972084 |
| Note | For research use only. |

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