Product nameAnti-1-methyladenosine (m1A) antibody [EPR-19836-208] - BSA and Azide free
See all 1-methyladenosine (m1A) primary antibodies
DescriptionRabbit monoclonal [EPR-19836-208] to 1-methyladenosine (m1A) - BSA and Azide free
Has been developed to discriminate between the modified base 1-methyladenosine (m1A) and the unmodified counterpart Adenosine (A).
Tested applicationsSuitable for: Dot blot, ELISA, IPmore details
Species reactivityReacts with: Synthetic fragment
Chemical/ Small Molecule corresponding to 1-methyladenosine (m1A).
Ab251495 is the carrier-free version of ab208196. This format is designed for use in antibody labeling, including fluorochromes, metal isotopes, oligonucleotides, enzymes.
Our carrier-free formats are supplied in a buffer free of BSA, sodium azide and glycerol for higher conjugation efficiency.
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.
ab251495 is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm.
Maxpar® is a trademark of Fluidigm Canada Inc.
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 rabbit monoclonal antibody.
Storage instructionsShipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term. Avoid freeze / thaw cycle.
Concentration information loading...
Our Abpromise guarantee covers the use of ab251495 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|Dot blot||Use at an assay dependent concentration.|
|ELISA||Use at an assay dependent concentration.|
|IP||Use at an assay dependent concentration.|
- 1 methyladenosine antibody
- 1-methyladenosine antibody
- m1A antibody
ab251495 has not yet been referenced specifically in any publications.