Anti-N6, N6-dimethyladenosine (m6,6A) 抗体 [EPR- 19831-44]
Anti-N6, N6-dimethyladenosine (m6,6A) antibody [EPR- 19831-44]
- RabMAb
- Recombinant
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(2 Publications)
Rabbit Recombinant Monoclonal N6, N6-dimethyladenosine (m6,6A) antibody. Suitable for IP, ELISA and reacts with Modified Nucleic Acid samples. Cited in 2 publications.
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Di-m6A, N6, N6 dimethyladenosine
- ELISA
Lab
ELISA - Anti-N6, N6-dimethyladenosine (m6,6A) antibody [EPR- 19831-44] (AB208198)
Biotinylated m6,6A (modified), m6A (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.[m6,6A]*.mN.mN.mN.mN.mN 3'
Modified oligonucleotide (5 μM), 5' Biotin-mN.mN.mN.mN.mN.[m6A]*.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 ab208198 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.
- IP
Supplier Data
Immunoprecipitation - Anti-N6, N6-dimethyladenosine (m6,6A) antibody [EPR- 19831-44] (AB208198)
The IP was performed in a U-bottom non-adsorbing propylene 96-well plate.
ab208198 (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.[m6,6A]*.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 and concentration : 5% NFDM/TBST
Dilution buffer and concentration : TBST/0.1% Triton X-100/1 mM EDTA
All lanes:
Immunoprecipitation - Anti-N6, N6-dimethyladenosine (m6,6A) antibody [EPR- 19831-44] (ab208198)
false
関連する標識済み抗体及び組成の異なる製品 (1)
-
Anti-N6, N6-dimethyladenosine (m6,6A) antibody [EPR- 19831-44] - BSA and Azide free
Reactivity data
製品の詳細
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
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製品の状態
精製方法
バッファー組成
出荷温度
短期保存期間
短期保存温度
長期保存温度
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補足情報
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
M66A can affect RNA's structural configuration and its interaction with other molecules. It is a part of the broader modification network within RNAs often found with other RNA modifications such as m6A and m1A. The presence of m66A influences RNA stability splicing and export which can alter the outcome of gene expression. In the context of gene expression regulation m66A interacts with multiple proteins that recognize and modify RNA structures. Consequently it forms part of the dynamic and responsive mechanisms that control cellular activities.
Pathways
M66A participates in the RNA metabolism and gene expression pathways. It associates with critical biological functions through interactions with proteins like METTL3 and FTO which regulate RNA methylation status. These pathways are important for processes such as translation regulation and RNA decay. METTL3 a methyltransferase adds methyl groups to RNA while FTO a demethylase removes them creating a balance in the modification states essential for proper cellular function.
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文献 (2)
Recent publications for all applications. Explore the full list and refine your search
Annals of medicine 57:2546670 PubMed40798940
2025
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Advanced science (Weinheim, Baden-Wurttemberg, Germany) 12:e2417067 PubMed40019372
2025
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