Summary & Explanation
{"type":"root","children":[{"type":"paragraph","children":[{"type":"text","value":"Wilms’ Tumor Protein (WT1) is a suppressor gene located on Chromosome 11p13. Mutations of the WT1 gene on Chromosome 11 are observed in approximately 20% of Wilms tumors. At least half of the Wilms tumors with mutations in WT1 also carry mutations in CTNNB1, the gene encoding the proto-oncogene beta-catenin."}]},{"type":"paragraph","children":[{"type":"text","value":"Wilms’ tumor is a neoplasm of the kidneys that typically occurs in children. It is also known as a Nephroblastoma. WT1 has been identified in proliferative mesothelial cells, Malignant Mesothelioma, Ovarian Cystadenocarcinoma, Gonadoblastoma, Nephroblastoma and Desmoplastic Small Round Cell Tumor. Lung Adenocarcinomas\n rarely stain positive with this antibody."}]}]}
Antibody Type
Mouse Monoclonal
Clone
6F-H2
Isotype
IgG1/K
Localization
Nuclear
Dilution
1:100-1:500
Species Reactivity
Human
Immunogen
Recombinant protein corresponding to amino acids 1-181 of human WT1.
