Anti-N2,N2-dimethylguanosine (m2,2G) antibody [EPR-19838-40]
- 20ul selling size
- RabMAb
- Recombinant
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(3 Publications)
Rabbit Recombinant Monoclonal N2,N2-dimethylguanosine (m2,2G) antibody. Suitable for Dot, IP, ELISA and reacts with Modified Nucleic Acid samples. Cited in 3 publications.
View Alternative Names
Di-m2G, N2,N2-dimethylguanosine, m22G
- IP
Supplier Data
Immunoprecipitation - Anti-N2,N2-dimethylguanosine (m2,2G) antibody [EPR-19838-40] (AB211488)
The IP was performed in a U-bottom non-adsorbing propylene 96-well plate.
ab211488 (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.[m2,2G]*.mN.mN.mN.mN.mN 3'
Lane 3 : Unmodified oligonucleotide (5 μM), 5' Biotin-mN.mN.mN.mN.mN.[G]*.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-N2,N2-dimethylguanosine (m2,2G) antibody [EPR-19838-40] (ab211488)
true
- ELISA
Supplier Data
ELISA - Anti-N2,N2-dimethylguanosine (m2,2G) antibody [EPR-19838-40] (AB211488)
BSA-conjugated m22G (modified) and G (unmodified) nucleosides were coated onto wells of a 96 well plate. ELISA was performed on 1.0 μg/ml of antigen using ab211488 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.
- Dot
Lab
Dot Blot - Anti-N2,N2-dimethylguanosine (m2,2G) antibody [EPR-19838-40] (AB211488)
Primary antibody dilution : 1/500
Secondary antibody : Goat Anti-Rabbit IgG (H+L) Peroxidase conjugated
Secondary antibody dilution : 1/100000
Blocking and dilution buffer : AdvanBlockTM Chemi Blocking buffer
Input : Biotin-m2.2G oligo 2 ng per Dot
Competitive nucleosides : m2.2G m2G m1G
Exposure times : 37 seconds
- Dot
Lab
Dot Blot - Anti-N2,N2-dimethylguanosine (m2,2G) antibody [EPR-19838-40] (AB211488)
Lane 1 : Yeast tRNA
Lane 2 : Biotin-m2.2G RNA oligo
Lane 3 : Biotin-G RNA oligo
Primary antibody dilution : 1/500
Secondary antibody : Goat Anti-Rabbit IgG (H+L) Peroxidase conjugated
Secondary antibody dilution : 1/20000
Blocking and dilution buffer : AdvanBlockTM Chemi Blocking buffer
Related conjugates and formulations (1)
-
Anti-N2,N2-dimethylguanosine (m2,2G) antibody [EPR-19838-40] - BSA and Azide free
Reactivity data
Product details
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The modification of guanine at the N2 position influences RNA stability and function by enhancing the efficiency of translation. It forms part of the ribosome's active sites appearing as part of larger ribonucleoprotein complexes which are important for carrying out protein synthesis. This modification helps maintain the correct structure of ribosomal RNA ensuring accurate and efficient protein production. The presence of m22G in RNA components aids in the prevention of frameshift mutations during translation marking its importance in maintaining genetic fidelity.
Pathways
M22G plays a significant role in the translation and protein synthesis pathway contributing to the proper assembly and function of ribosomes. The presence of m22G within these pathways ensures the proper execution of genetic code translation interacting closely with proteins like ribosomal protein S15 and other translational machinery components. These interactions are essential in coordinating the synthesis of proteins impacting cellular growth and development functions.
Product protocols
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Publications (3)
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STAR protocols 6:103924 PubMed40601427
2025
Applications
Unspecified application
Species
Unspecified reactive species
ACS chemical biology 17:2789-2800 PubMed36190452
2022
Applications
Unspecified application
Species
Unspecified reactive species
Scientific reports 7:11383 PubMed28900184
2017
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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