Anti-1-methylguanosine (m1G) antibody [EPR19833-150]
- 20ul selling size
- RabMAb
- Recombinant
- What is this?
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- Dot
Supplier Data
Dot Blot - Anti-1-methylguanosine (m1G) antibody [EPR19833-150] (AB208199)
Dot blot analysis of 1-methylguanosine (m1G) using ab208199 at 1/500 dilution, followed by Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1/20,000 dilution (Left) or Methylene Blue (Right).
Lane 1 : HeLa total RNA
Lane 2 : Yeast tRNA
Exposure time : 8 seconds
- ELISA
Supplier Data
ELISA - Anti-1-methylguanosine (m1G) antibody [EPR19833-150] (AB208199)
BSA-conjugated m1G (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 ab208199 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-1-methylguanosine (m1G) antibody [EPR19833-150] (AB208199)
The IP was performed in a U-bottom non-adsorbing propylene 96-well plate.
ab208199 (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.[m1G]*.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-1-methylguanosine (m1G) antibody [EPR19833-150] (ab208199)
true
- FRET
Supplier Data
FRET - Anti-1-methylguanosine (m1G) antibody [EPR19833-150] (AB208199)
A FRET-based assay was performed using 25 nm of each biotinylated oligo using ab208199 at a concentration range of 0.001-4.000 µg/ml.
- Dot
Supplier Data
Dot Blot - Anti-1-methylguanosine (m1G) antibody [EPR19833-150] (AB208199)
Dot blot analysis of 1-methylguanosine (m1G) using ab208199 at 1/500 dilution, followed by Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1/20,000 dilution (Upper) or a Streptavidin-Alexa®488 conjugate (Lower).
Lane 1 : Biotin-m1G RNA oligo
Lane 2 : Biotin-G RNA oligo
Lane 3 : Biotin-m2G RNA oligo
Lane 4 : Biotin-m22G RNA oligo
Exposure time 5 seconds
Related conjugates and formulations (1)
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Anti-1-methylguanosine (m1G) antibody [EPR19833-150] - 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
M1G impacts RNA functionality by influencing RNA folding and structural conformation. It forms integral parts of RNA molecules and contributes to their stability and function. m1G does not act in isolation but is part of a broader set of modified nucleosides that collectively enhance RNA function. The modifications involving m1G occur as part of post-transcriptional modification processes. These are often important for ensuring proper decoding and function of RNA during gene expression.
Pathways
Research indicates that the presence of m1G within RNA molecules can influence specific biological pathways related to translation and RNA stability. m1G impacts the efficiency and fidelity of translational machinery playing a part in the translation pathway. Additionally it interacts with various proteins like tRNA methyltransferases which facilitate its methylation in RNA. These enzymes are critical in pathways that ensure the correctness of RNA modifications which ultimately influence protein synthesis.
Product protocols
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Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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