Key features and details
- Rabbit polyclonal to GBAS
- Suitable for: ICC/IF, IHC-P, WB
- Reacts with: Human
- Isotype: IgG
Product nameAnti-GBAS antibody
See all GBAS primary antibodies
DescriptionRabbit polyclonal to GBAS
Tested applicationsSuitable for: ICC/IF, IHC-P, WBmore details
Species reactivityReacts with: Human
- A-431 cells; RT-4, U-251 MG, liver and tonsil lysates; Human heart muscle tissue.
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: 7.20
Preservative: 0.02% Sodium azide
Constituents: 59% PBS, 40% Glycerol
Concentration information loading...
PurityImmunogen affinity purified
Our Abpromise guarantee covers the use of ab204890 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|ICC/IF||Use a concentration of 0.25 - 2 µg/ml.|
|IHC-P||1/2500 - 1/5000. Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.|
|WB||Use a concentration of 0.04 - 0.4 µg/ml. Predicted molecular weight: 34 kDa.|
Tissue specificityWidely expressed. Most abundant in heart and skeletal muscle.
Sequence similaritiesBelongs to the NipSnap family.
- Information by UniProt
- 4 nitrophenylphosphatase domain and non neuronal SNAP25 like 2 antibody
- gbas antibody
- Glioblastoma amplified sequence antibody
All lanes : Anti-GBAS antibody (ab204890) at 1/250 dilution
Lane 1 : RT-4 cell lysate
Lane 2 : U-251 cell lysate
Lane 3 : Human plasma lysate
Lane 4 : Human liver lysate
Lane 5 : Human tonsil lysate
Predicted band size: 34 kDa
Immunofluorescent analysis of PFA/Triton X-100 fixed and permeabilized A-431 cells labeling GBAS with ab204890 at 4 µg/ml. Antibody staining is shown in green.
Immunohistochemical analysis of formalin-fixed. paraffin-embedded Human heart muscle labeling GBAS with ab204890 at 1/2500.
ab204890 has not yet been referenced specifically in any publications.