Product nameAnti-ADFP antibody [EPR3713] (HRP)
See all ADFP primary antibodies
DescriptionRabbit monoclonal [EPR3713] to ADFP (HRP)
Tested applicationsSuitable for: WBmore details
Species reactivityReacts with: Mouse, Rat
Predicted to work with: Human
Synthetic peptide within Human ADFP aa 1-100. The exact sequence is proprietary.
Database link: Q99541
- WB: Mouse brain and Rat brain tissue lysates.
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. Stable for 12 months at -20°C. Store In the Dark.
Storage bufferpH: 7.4
Preservative: 0.1% Proclin
Constituents: 30% Glycerol, 1% BSA, PBS
Concentration information loading...
PurityProtein A purified
- Pathways and Processes
- Metabolic signaling pathways
- Lipid and lipoprotein metabolism
- Lipid metabolism
Our Abpromise guarantee covers the use of ab201721 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|WB||1/5000. Detects a band of approximately 48 kDa (predicted molecular weight: 48 kDa).|
FunctionMay be involved in development and maintenance of adipose tissue.
Tissue specificityMilk lipid globules.
Sequence similaritiesBelongs to the perilipin family.
modificationsAcylated; primarily with C14, C16 and C18 fatty acids.
- Information by UniProt
- ADFP antibody
- Adipophilin antibody
- Adipose differentiation related protein antibody
All lanes : Anti-ADFP antibody [EPR3713] (HRP) (ab201721) at 5000 µg
Lane 1 : Brain (Mouse) Tissue Lysate
Lane 2 : Brain (Rat) Tissue Lysate
Lysates/proteins at 10 µg per lane.
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 48 kDa
Observed band size: 48 kDa
Exposure time: 30 seconds
This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 3% milk before being incubated with ab201721 overnight at 4°C. Antibody binding was visualised using ECL development solution ab133406.
ab201721 has not yet been referenced specifically in any publications.