Rabbit Recombinant Monoclonal 2-methyladenosine (m2A) antibody. Carrier free. Suitable for IP, ELISA and reacts with Modified Nucleic Acid samples.
pH: 7.2 - 7.4
Constituents: PBS
IP | ELISA | |
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Modified Nucleic Acid | Tested | Tested |
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 - |
2-methyladenosine, m2A
Rabbit Recombinant Monoclonal 2-methyladenosine (m2A) antibody. Carrier free. Suitable for IP, ELISA and reacts with Modified Nucleic Acid samples.
pH: 7.2 - 7.4
Constituents: PBS
Has been developed to discriminate between the modified base 2-methyladenosine (m2A) and the unmodified counterpart Adenosine (A).
ab251530 is the carrier-free version of Anti-2-methyladenosine (m2A) antibody [EPR -19851-59] ab211495.
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.
This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
2-methyladenosine (m2A) is a modified nucleoside that plays a significant role in RNA structures impacting RNA stability and function. It is an adenosine derivative where a methyl group is added to the nitrogen at position 2 of the adenine ring altering its chemical properties. This modification has a relatively small molecular mass of approximately 281.3 Da. m2A is found primarily in tRNA and rRNA molecules within the cell contributing to their proper folding and stability. It is ubiquitously expressed across various tissues reflecting its broad functional significance.
The modification of RNA by 2-methyladenosine contributes significantly to RNA processing and function. It plays a role in the structural integrity and proper folding of tRNA and rRNA by maintaining the stability of the RNA molecules they modify. m2A acts within ribonucleoprotein complexes where it influences the recognition and interaction between RNA and protein components. This modification ensures the accuracy of translation by maintaining the correct conformation of the RNA molecules involved in protein synthesis.
2-methyladenosine engages in essential biological processes such as translation and RNA processing. It is involved in the ribosome biogenesis pathway which is important for protein synthesis in cells. Within this pathway m2A interacts with other RNA modifications and proteins like the ribosomal proteins and various RNA-binding proteins that guide RNA through the maturation process. The presence of m2A aids the efficient assembly of ribosomal units necessary for the synthesis of proteins.
Altered levels of 2-methyladenosine have been implicated in disorders related to dysfunction in protein synthesis. Aberrant m2A modification has been linked to certain cancers wherein improper RNA processing might contribute to uncontrolled cellular proliferation. Additionally it relates to neurodegenerative diseases where misfolded proteins result from translation dysregulation. In this context m2A modifications can affect the function of proteins such as ribosome-associated proteins and those involved in RNA methylation influencing disease outcomes through changes in RNA stability and processing.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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In the unlikely event of one of our products not working as expected, you are covered by our product promise.
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Terms & Conditions.
This data was developed using Anti-2-methyladenosine (m2A) antibody [EPR -19851-59] ab211495, the same antibody clone in a different buffer formulation.
The IP was performed in a U-bottom non-adsorbing propylene 96-well plate.
Anti-2-methyladenosine (m2A) antibody [EPR -19851-59] ab211495 (0.2 μg) was coated into Dynabeads® sheep-anti-rabbit IgG (50 μl) for 1h at RT.
Unmodified/modified oligonucleotides (5 μM) were added to samples containing the antibody/bead complexes and incubated with agitation for 1 hour at RT.
After washing, Peroxidase-conjugated Streptavidin was incubated at 1/1000 dilution with agitation for 1 hour at RT.
ECL substrate was then added and the results read in a non-transparent 96-well plate with a digital detector and analyzed using ImageJ.
Lane 1: Buffer only.
Lane 2: Modified oligonucleotide (5 μM), 5' Biotin-mN.mN.mN.mN.mN.[ m2A]*.mN.mN.mN.mN.mN 3'
Lane 3: Unmodified oligonucleotide (5 μM), 5' Biotin-mN.mN.mN.mN.mN.[A]*.mN.mN.mN.mN.mN 3'
N - equimolar mixture of (A/U/G/C)
m - 2'O methyl protection
* - phosphorothioate protection
Blocking buffer: 5% NFDM/TBST
Dilution buffer: TBST/0.1% Triton X-100/1 mM EDTA.
All lanes: Immunoprecipitation - Anti-2-methyladenosine (m2A) antibody [EPR -19851-59] (Anti-2-methyladenosine (m2A) antibody [EPR -19851-59] ab211495)
Developed using the ECL technique.
This data was developed using Anti-2-methyladenosine (m2A) antibody [EPR -19851-59] ab211495, the same antibody clone in a different buffer formulation.Biotinylated m2A (modified) and A (unmodified) oligonucleotides with the below sequence were coated onto wells of a 96 well plate. Modified oligonucleotide (5 μM), 5’ Biotin-mN.mN.mN.mN.mN.[ m2A]*.mN.mN.mN.mN.mN 3’ Unmodified oligonucleotide (5 μM), 5’ Biotin-mN.mN.mN.mN.mN.[A]*.mN.mN.mN.mN.mN 3’ N - equimolar mixture of (A/U/G/C)
m - 2’O methyl protection
* - phosphorothioate protection ELISA was performed on 1.0 µg/ml of antigen using Anti-2-methyladenosine (m2A) antibody [EPR -19851-59] ab211495 at a concentration range of 0.005-4.000 µg/ml, followed by Goat Anti-Rabbit IgG, (H+L), alkaline phosphatase conjugated secondary antibody at 1/2500 dilution.
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