| Product Name | DP2 antibody |
|---|---|
| Antibody Type | Primary Antibodies |
| Product description | Mouse monoclonal [BC - 2] to DP2The metabolic function of the APC gene is not known. Defects in this gene cause familial adenomatous polyposis (FAP), an autosomal dominant pre-malignant disease that usually progresses to malignancy. Disease-associated mutations tend to be clustered in a small region designated the mutation cluster region (MCR) and result in a truncated protein product. |
| Immunogen | Recombinant DP2 protein (Human) |
| Clonality | Monoclonal |
|---|---|
| Isotype | IgG1 |
| Host Species | Mouse |
| Tested Applications | EMSAIPWB |
| EMSA: Use at an assay dependent dilution. WB: 0.5-1?ug/mL using a whole extract of transfected 293T (human embryonal kidney) cells expressing DP2 IP: suitable using native and denatured DP2. Optimal dilutions/concentrations should be determined by the end user.: |
|
| Species Reactivity | Human |
| Concentration | 0.5mg/ml |
| Purification | Affinity purified |
| Gene Synonyms | Q14188 Dp-2 602160 TFDP2 Dp2 7029 Dp 2 |
|---|
| Application Notes | EMSA: Use at an assay dependent dilution. WB: 0.5-1?ug/mL using a whole extract of transfected 293T (human embryonal kidney) cells expressing DP2 IP: suitable using native and denatured DP2. Optimal dilutions/concentrations should be determined by the end user.: |
|---|
| Form | Liquid |
|---|---|
| Storage Instructions | Keep as concentrated solution. Store at 4ºC short term. For extended storage aliquot and store at -20ºC or below. Avoid freeze-thaw cycles. |
| Storage Buffer | Phosphate-buffered saline, pH 7.2, |
