Anti-N6-methyladenosine (m6A) antibody [17-3-4-1] (ab208577) is a mouse monoclonal antibody detecting N6-methyladenosine (m6A) in IP.
- Over 60 publications
Preservative: 0.02% Sodium azide
Constituents: 99.98% PBS
IP | SB | Northwestern | |
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Modified Nucleic Acid | Tested | Tested | Tested |
Species | Dilution info | Notes |
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Species Modified Nucleic Acid | Dilution info - | Notes Best results are obtained by pre-binding the antibody to the beads before washing off unbound immunoglobulin. It is recommended to start with an excess of antibody in order to ensure the Protein G beads are saturated.Used 3μg in 500μl for IP which yielded positive results. |
Species | Dilution info | Notes |
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Species Modified Nucleic Acid | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Modified Nucleic Acid | Dilution info - | Notes - |
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N6-methyladenosine, m6A
Anti-N6-methyladenosine (m6A) antibody [17-3-4-1] (ab208577) is a mouse monoclonal antibody detecting N6-methyladenosine (m6A) in IP.
- Over 60 publications
Preservative: 0.02% Sodium azide
Constituents: 99.98% PBS
This antibody recognises N6-methyladenosine in both modified RNA and DNA.
N6-methyladenosine (m6A) is a chemical modification present in RNA molecules specifically marking the adenosine base with a methyl group at the nitrogen-6 position. This modification weighing approximately 14 Da occurs in diverse eukaryotic species and influences RNA metabolism. m6A methylation can be detected using techniques like m6A dots blot or m6A ELISA. The modification is abundant in tissues like the brain and testis reflecting its critical role in varying cell types. Also m6A is known as a dynamic and reversible mark with its levels continuously adjusted by enzymes called writers (methyltransferases) erasers (demethylases) and readers (RNA-binding proteins).
M6A methylation affects mRNA processing stability translation and decay. It integrates into large multi-protein complexes where it influences gene expression outcomes by affecting the RNA's interaction with the cellular machinery. This methylation modification acts as a regulatory signal that influences essential processes such as cell differentiation and circadian rhythms. Elucidating the biological functions of m6A involves studying how it affects RNA fate and its downstream gene regulatory networks.
M6A modification is central to the mRNA metabolic pathway and the PI3K-Akt signaling pathway. It interacts with various proteins such as METTL3 an m6A methyltransferase which is vital for mediating m6A modification. It also interacts with YTH domain-containing proteins that recognize m6A marks influencing transcript dynamics and gene expression. The interplay of m6A with proteins in these pathways underlines its role in fine-tuning cellular processes and responses.
M6A modification has a significant impact on cancer and neurological disorders. In cancers alterations in m6A methylation patterns can promote oncogenic transformation and metastasis. m6A-related proteins such as FTO an m6A demethylase have shown connections to these pathways affecting cancer progression. In neurological disorders m6A impacts aspects of neural development and function and abnormalities in its regulation may contribute to diseases like Alzheimer's. Understanding the roles of m6A in diverse diseases can pave the way for novel therapeutic approaches.
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N6-methyladenosine (m6A) was immunoprecipitated using ab208577 from radiolabeled synthetic methylated transcript (Bound); radiolabeled Non methylated control (Non bound) and radiolabeled Input RNA control.
All lanes: Immunoprecipitation - Anti-N6-methyladenosine (m6A) antibody [17-3-4-1] (ab208577)
Use of ab208577 for northwestern blot using synthetic methlyated and non methlyated RNA.
Lane 2 Double stranded DNA
Labelled with ab208577. Arrow shows m6A containing fragment.
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