Recombinant Human ADAT2 protein is a Human Full Length protein, in the 1 to 191 aa range, expressed in Escherichia coli, with >90% purity and suitable for SDS-PAGE, MS.
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Application | Reactivity | Dilution info | Notes |
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Application SDS-PAGE | Reactivity Reacts | Dilution info - | Notes - |
Application MS | Reactivity Reacts | Dilution info - | Notes - |
Probably participates in deamination of adenosine-34 to inosine in many tRNAs.
DEADC1, ADAT2, tRNA-specific adenosine deaminase 2, Deaminase domain-containing protein 1, tRNA-specific adenosine-34 deaminase subunit ADAT2
Recombinant Human ADAT2 protein is a Human Full Length protein, in the 1 to 191 aa range, expressed in Escherichia coli, with >90% purity and suitable for SDS-PAGE, MS.
pH: 8
Constituents: 10% Glycerol (glycerin, glycerine), 0.316% Tris HCl, 0.29% Sodium chloride, 0.0308% (R*,R*)-1,4-Dimercaptobutan-2,3-diol
Probably participates in deamination of adenosine-34 to inosine in many tRNAs.
Belongs to the cytidine and deoxycytidylate deaminase family. ADAT2 subfamily.
ADAT2 also known as ADAT2 deaminase plays an important role in RNA editing by converting adenosines to inosines in tRNA molecules. This deaminase has a mass of roughly 50 kDa and is widely expressed in various tissues. Its presence is important for maintaining RNA stability and accurate coding which together plays pivotal part in protein synthesis.
ADAT2 works as part of the ADAT complex that includes ADAT3. This complex specifically targets anticodon regions of tRNAs. The conversion of adenosine to inosine by ADAT2 changes the reading of certain codons allowing for proper interpretation of genetic code elements important for cell function and viability. ADAT2’s activity impacts the modification process essential for accurate protein translation.
Four important mechanisms involve ADAT2 in RNA metabolic processes. It plays an integral role in the post-transcriptional modification of RNA particularly within the tRNA maturation pathway. This pathway collaborates with proteins such as ADAT3 and their interaction governs fidelity in transcribing genetic information into proteins. The editing by ADAT2 ensures that tRNA molecules can correctly interpret codons during translation.
Four recognized conditions involve faulty ADAT2 activity: one is neurodevelopmental disorders where genetic mutations affecting its function impact brain development. Another is some types of cancer where RNA editing disruptions play part in tumorigenic processes. These diseases can involve interactions with other proteins like ADAT3 that need for proper RNA editing balance. Understanding these interactions may help in developing therapeutic strategies targeting RNA editing mechanisms.
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ab101153 used in 15% SDS-PAGE (3 μg)
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