GLPBio

N6-Methyladenosine-5'-Triphosphate

Catalog No.: GN20007Purity:>99.00%

نوكليوزيد N6-مثيل أدينوزين (N6-methyl ATP) هو تحول قاعدي معدّل لأدينوزين وهو يتم العثور عليه كنكليوسايد صغير في الرنا الطبيعية (Meyer et al.).

المنتجات مخصصة للاستخدام البحثي فقط، وليست للاستخدام البشري. نحن لا نبيع للمرضى.


N6-Methyladenosine-5'-Triphosphate
10ul (100 mM)In Stock
$78.00
1
50ul (100 mM)In Stock
$330.00
1
100ul (100 mM)In Stock
$616.00
1

المراجع (Citations)

لا تتوفر حاليًا مراجع لهذا المنتج. فيما يلي مجموعة مختارة من المنشورات التي تستشهد بمنتجات GlpBio.
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    641, 529–536 (2025)
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    632, 686–694 (2024)
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    618, 1017–1023 (2023)
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    610, 366–372 (2022)
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    Cell
    187(9):2288-2304 (2024)
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    183(7):1867-1883 (2020)
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    388(6745) (2025)
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    31, 1291–1307 (2021)

الوصف (Description)

N6-Methyladenosine-5-Triphosphate (N6-methyl ATP; m6ATP) is a base-modified analog of adenosine, identified as a minor nucleoside in natural RNA[1]. N6-Methyladenosine-5’-Triphosphate is a dynamic, reversible, covalent modification of ribonucleotides, commonly found in eukaryotic messenger RNA (mRNA), and plays a crucial regulatory role in RNA splicing, export, stability, and translation[2, 3]. N6-Methyladenosine-5-Triphosphate serves as a substrate for RNA polymerase and is used as a complete substitute for ATP in mRNA modification reactions[4, 5]. Additionally, N6-Methyladenosine-5-Triphosphate is an effective agonist for P2Y purinergic receptors in guinea pigs and Escherichia coli[6]. This product is provided in the form of a lithium salt solution.

References:
[1] Yuan Y, Arneson R, Burke E, et al. Efficient 3′-end tailing of RNA with modified adenosine for nanopore direct total RNA sequencing[J]. bioRxiv, 2024: 2024.02. 24.581884.
[2] Zheng H, Li S, Zhang X, et al. Functional implications of active N6-methyladenosine in plants[J]. Frontiers in Cell and Developmental Biology, 2020, 8: 291.
[3] Anderson S J, Kramer M C, Gosai S J, et al. N6-methyladenosine inhibits local ribonucleolytic cleavage to stabilize mRNAs in Arabidopsis[J]. Cell reports, 2018, 25(5): 1146-1157. e3.
[4] Parr C J C, Wada S, Kotake K, et al. N 1-Methylpseudouridine substitution enhances the performance of synthetic mRNA switches in cells[J]. Nucleic Acids Research, 2020, 48(6): e35-e35.
[5] Potapov V, Fu X, Dai N, et al. Base modifications affecting RNA polymerase and reverse transcriptase fidelity[J]. Nucleic Acids Research, 2018, 46(11): 5753-5763.
[6] Burnstock G, Fischer B, Hoyle C H V, et al. Structure activity relationships for derivatives of adenosine‐5′‐triphosphate as agonists at P2 purinoceptors: Heterogeneity within P2x and P2y subtypes[J]. Drug development research, 1994, 31(3): 206-219.

وثائق المنتج (Product Documents)

Purity:>99.00%

الخصائص الكيميائية (Chemical Properties)

النقاوة
>99.00%
معامل الانقراض
15,567 Lmol-1cm-1 at 265 nm
الصيغة
C11H18N5O13P3 (free acid)
M.Wt
521.20 g/mole (free acid)
الشكل الملحي
Li+
التركيز
100 mM
المحلول المنظم
H2O
التخزين
-20°C or below
المرادفات
N6-Methyl-ATP, m6ATP
الهيكل الأساسي
5'-Triphosphate
نظير القاعدة
Adenosine
نوع السكر
RNA
فئة النيوكليوتيد
Base Modified RNA
التطبيقات
Aptamers, Epigenetics/DNA Damage, In vitro Transcription, Mutagenesis, Photocrosslinking Studies

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