TRP53 antibody | knockout validation | Novocastra NCL-p53-CM5p
DOI
//dx.doi.org/10.13070/ko.en.7.2207
Date
2017-03-18

This is a knockout-validated antibody summary, based on the publication "An inducible lentiviral guide RNA platform enables the identification of tumor-essential genes and tumor-promoting mutations in vivo", as cited below [1]. Labome curates formal publications to compile a list of antibodies with unambiguous specificity within Validated Antibody Database (VAD).

TRP53 antibody | knockout validation | Novocastra NCL-p53-CM5p figure 1
Figure 1. (Upper panel) Western blot analysis of each lymphoma for TRP53 protein and p19 with probing for b-actin used as a loading control. 41.2% of Eμ-Myc isgTrp53 tumors assessed display abnormally high (stabilized) TRP53 protein, indicative of mutations in Trp53. (Lower panel) Western blot analysis of lymphomas before and after treatment with etoposide (0.5 mg/ml for 24 hr) in the presence of the broad-spectrum caspase inhibitor QVD-OPH (25 mM) to prevent apoptosis. i: inducible, cont: constitutive. From [1].
Antibody information

Rabbit polyclonal IgG

Company: Novocastra

Antibody: TRP53

Catalog number: NCL-p53-CM5p

Summary: Rabbit polyclonal IgG against recombinant mouse p53 protein. Reacts with mouse and rat. Suitable for western blot and immunohistochemistry (paraffin).

Validation Method

Western blot

Sample

Tumors formed by injection of Eμ-Myc lymphoma cells having WT, mutated or deleted p53. Cells and primary tumor samples were lysed in RIPA buffer supplemented with protease inhibitors (complete protease inhibitor cocktail, Roche).

Blocking agent

5% milk in PBS with 0.1% Tween 20.

References
  1. Aubrey B, Kelly G, Kueh A, Brennan M, O'Connor L, Milla L, et al. An inducible lentiviral guide RNA platform enables the identification of tumor-essential genes and tumor-promoting mutations in vivo. Cell Rep. 2015;10:1422-32 pubmed publisher