Key features and details
- Rabbit polyclonal to DPP3
- Suitable for: WB, IP
- Reacts with: Mouse, Human
- Isotype: IgG
Product nameAnti-DPP3 antibody
See all DPP3 primary antibodies
DescriptionRabbit polyclonal to DPP3
Tested applicationsSuitable for: WB, IPmore details
Species reactivityReacts with: Mouse, Human
Predicted to work with: Rat
- HeLa, 293T, Jurkat, TCMK1 and NIH 3T3 cell lysates.
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 bufferpH: 7
Preservative: 0.09% Sodium azide
Constituent: 99% Tris citrate/phosphate
pH 7.0 to 8.0
Concentration information loading...
PurityImmunogen affinity purified
Purification notesab217127 was affinity purified using an epitope specific to DPP3 immobilized on solid support.
Our Abpromise guarantee covers the use of ab217127 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|WB||1/2000 - 1/10000. Predicted molecular weight: 83 kDa.|
|IP||Use at 2-10 µg/mg of lysate.|
Sequence similaritiesBelongs to the peptidase M49 family.
- Information by UniProt
- Dipeptidyl aminopeptidase III antibody
- Dipeptidyl arylamidase III antibody
- Dipeptidyl peptidase 3 antibody
All lanes : Anti-DPP3 antibody (ab217127) at 0.1 µg/ml
Lane 1 : HeLa whole cell lysate
Lane 2 : 293T whole cell lysate
Lane 3 : Jurkat whole cell lysate
Lane 4 : TCMK1 whole cell lysate
Lane 5 : NIH 3T3 whole cell lysate
Lysates/proteins at 15 µg per lane.
Developed using the ECL technique.
Predicted band size: 83 kDa
Exposure time: 30 seconds
Lysis buffer: NETN
Detection of DPP3 in Immunoprecipitates of 293T whole cell lysates (1 mg for IP, 20% of IP loaded) using ab217127 at 6 µg/mg lysate for IP (Lane 1). For WB detection ab217127 was used at 1µg/ml. Lane 2 Control IgG IP. Detection: Chemiluminescence with an exposure time of 10 seconds.
ab217127 has not yet been referenced specifically in any publications.