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Anti-ADAR/IFI4 Polyclonal Antibody (HX876014)

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Aperçu
Numéro de catalogueHX876014
Description
Anti-ADAR/IFI4 Polyclonal Antibody (HX876014) is a rabbit polyclonal antibody detecting ADAR in ELISA, IHC, WB. Suitable for Human and Rat.
Highlights
  • ●Affinity Purified — Minimal background and high purity for reliable results.
  • ●Multi-Application — Validated across multiple applications.
Reactivité des espècesHuman
ApplicationsELISA, IHC, WB
Espèce hôteRabbit
ClonalitéPolyclonal
IsotypeIgG
Immunogène E. coli - derived recombinant Human ADAR/IFI4 (Asn503-Val885).
Cible 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
Purification Purified by antigen affinity column.
Numéro d'accès P55265
Forme Liquid
Tampon de stockage 0.01M PBS, pH 7.4, 50% Glycerol, 0.05% Proclin 300.

Reférez-vous aux informations spécifiques sur le tampon dans la copie papier du datasheet ou dans le COA spécifique au lot.

Informations d'utilisation du produit
Application Dilution
ELISA 1:5000-1:20000
IHC 1:50-1:500
WB 1:500-1:2000
Stabilité et stockage 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.
Contexte

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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Formula
Mass (g) = Concentration (mol/L) × Volume (L) × MW (g/mol)
Enter any 2 of Mass, Concentration, Volume + Molecular Weight to solve for the unknown.
Mass
=
Concentration
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Volume
Molecular Weight *
g/mol
Formula
C₁ × V₁ = C₂ × V₂
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Stock Solution
C₁ (Stock Conc.)
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V₁ (Stock Vol.)
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Working Solution
C₂ (Working Conc.)
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V₂ (Working Vol.)
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