Mouse anti-Wilms Tumor 1 Antibody DL99608A
Specifications
| 50µl / 100µl |
Background:
Mouse monoclonal antibody to Wilms Tumor 1
Alternative names:
Wilms tumor protein; WT33
Clonality:
Monoclonal
Species reactivity:
H
Host:
Mouse
Immunogen:
KLH-conjugated synthetic peptide encompassing a sequence within human Wilms Tumor 1. The exact sequence is proprietary.
Purification method:
The antibody was purified by immunogen affinity chromatography.
Concentration:
1mg/mL
Buffer:
Mouse IgG2b. Liquid in PBS containing 50% glycerol, 0.2% BSA and 0.01% sodium azide.
Applications:
IH
Recommended dilution:
IH (1/100 - 1/300)
Storage:
Shipped at 4°C. Upon delivery aliquot and store at -20°C for one year. Avoid freeze/thaw cycles.
WB description:
N/A
IHC description:
Immunohistochemical analysis of Wilms Tumor 1 staining in human mesothelioma formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
IF/ICC description:
Immunohistochemical analysis of Wilms Tumor 1 staining in human ovarian serous cystadenocarcinoma formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
IP description:
Immunohistochemical analysis of Wilms Tumor 1 staining in human wilms' tumor formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
FC description:
N/A
ChIP description:
N/A
More info:
Email: info@sobekbio.com
Orders:
Email: orders@sobekbio.com
