p53 Rabbit Monoclonal Antibody(ARA752)
WB | 1:1000-1:5000 |
IHC | 1:1000-1:2000 |
IF/ICC | 1:200-1:1000 |
Description | Rabbit Monoclonal Antibody to p53 |
Antibody Type | Primary antibody |
Predicted MW | 53kDa |
Immunogen | A synthetic peptide corresponding to residues on the N-terminus of human p53 was used as an immunogen. |
Purification | ProA affinity purified IgG |
Form/Buffer | PBS 59%, Sodium azide 0.01%, Glycerol 40%, BSA 0.27%. |
Alternative Names | P53; Cellular tumor antigen p53; Antigen NY-CO-13; Phosphoprotein p53; Tumor suppressor p53 |
Gene Symbol | TP53 |
Entrez Gene | 7157(Human) |
Swissprot | P04637 |
*Clone Number, Reactivity, Source/Host and Clonality can be found in the product name and Key Features section above.

All lanes: Anti-p53 antibody at 1:5,000 dilution
Predicted MW: 44 kDa
Observed MW: 53 kDa
Lane 1: A431
Lane 2: HaCat
Lane 3: T47D
Lysates at 10 µg per lane
2nd Ab:
GAR HRP(H+L) 1:10,000
Exposure: 30s

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human colonic adenocarcinoma tissue labelling p53 with ARA752 at 1:1,000. Heat mediated antigen retrieval was performed using Tris/EDTA buffer pH 9.0.

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human ovarian cancer tissue labelling p53 with ARA752 at 1:1,000. Heat mediated antigen retrieval was performed using Tris/EDTA buffer pH 9.0.

ARA752 staining p53 in A431 cells by IF/ICC (immunofluorescence/immunocytochemistry). Cells were fixed with paraformaldehyde, permeabilized with 0.1% Triton X-100 and blocked with 10% goat serum for half an hour at room temperature. Samples were incubated with primary antibody (1:1,000) at 4°C. An Alexa Fluor<sup>®</sup> 594-conjugated Goat Anti-Rabbit IgG polyclonal was used as the secondary antibody (1:500). DAPI (blue) was used as the nuclear counter stain.
Control: PBS and secondary antibody, An Alexa Fluor<sup>®</sup> 594-conjugated Goat Anti-Rabbit IgG (1:500).

Overlay histogram showing A431 cells stained with ARA752 (Red). The cells were fixed with 4% paraformaldehyde (10 min) and then permeabilized with 0.1% TritonX-100 for 15 min. The cells were then incubated in the antibody (ARA752, 1:100 dilution) in 1x PBS/1% BSA for 30 min at room temperature. The secondary antibody used was a Goat Anti-Rabbit Alexa Fluor<sup>®</sup> 488 (IgG H+L) at 1:2,000 dilution for 20 min at room temperature. Unlabelled sample (Black) was used as a control.
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