Product nameAnti-MEF2BNB antibody [EPR14012]
See all MEF2BNB primary antibodies
DescriptionRabbit monoclonal [EPR14012] to MEF2BNB
Tested applicationsSuitable for: WBmore details
Species reactivityReacts with: Mouse, Rat, Human
Recombinant fragment within Human MEF2BNB aa 1 to the C-terminus. The exact sequence is proprietary.
Database link: Q96FH0
- Human small intestine, prostate and skeletal muscle lysate
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 production
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
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.
Storage bufferPreservative: 0.01% Sodium azide
Constituents: 40% Glycerol, 59% PBS, 0.05% BSA
Concentration information loading...
PurityTissue culture supernatant
Our Abpromise guarantee covers the use of ab181872 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|WB||1/1000 - 1/10000. Detects a band of approximately 13 kDa (predicted molecular weight: 13 kDa).|
Sequence similaritiesBelongs to the MEF2BNB family.
- Information by UniProt
- MEF2B neighbor gene protein antibody
- mef2bnb antibody
- MF2NB_HUMAN antibody
- Protein MEF2BNB antibody
All lanes : Anti-MEF2BNB antibody [EPR14012] (ab181872) at 1/10000 dilution
Lane 1 : Human small intestine tissue lysate
Lane 2 : Human prostate tissue lysate
Lane 3 : Human skeletal muscle tissue lysate
Lysates/proteins at 10 µg per lane.
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab136636) at 1/500 dilution
Predicted band size: 13 kDa
Observed band size: 13 kDa
ab181872 has not yet been referenced specifically in any publications.