Application
Western blot analysis of TOB2 Antibody (N-term) in HepG2 cell line lysates (35ug/lane). TOB2 (arrow) was detected using the purified Pab.Application
Formalin-fixed and paraffin-embedded human lung carcinoma tissue reacted with TOB2 antibody (N-term), which was peroxidase-conjugated to the secondary antibody, followed by DAB staining. This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated.| Product Name | TOB2 Antibody (N-term) |
|---|---|
| Antibody Type | Primary Antibodies |
| Antigen Alias | TOB2; KIAA1663; TOB4; TROB2; Protein Tob2; Protein Tob4; Transducer of erbB-2 2 |
| Clonality | Polyclonal |
|---|---|
| Isotype | Ig |
| Host Species | Rabbit |
| Tested Applications | WBIHC |
| WB:1:100~500 IHC |
|
| Species Reactivity | Human |
| Concentration | 1mg/ml |
| Gene Synonyms | KIAA1663 TOB4 TROB2 |
|---|---|
| Alternative Names | TOB2 KIAA1663 TOB4 TROB2 Protein Tob2 Protein Tob4 Transducer of erbB-2 2 |
| Molecular Weight(MW) | 36632 Da |
| Function | Anti-proliferative protein inhibits cell cycle progression from the G0/G1 to S phases |
| Tissue Specificity | Ubiquitous. |
| Cellular Localization | Cytoplasm. |
| Entrez Gene | 10766 |
|---|
Application
Western blot analysis of TOB2 Antibody (N-term) in HepG2 cell line lysates (35ug/lane). TOB2 (arrow) was detected using the purified Pab.
Application
Formalin-fixed and paraffin-embedded human lung carcinoma tissue reacted with TOB2 antibody (N-term), which was peroxidase-conjugated to the secondary antibody, followed by DAB staining. This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated.| Application Notes | WB:1:100~500 IHC |
|---|
| Form | Liquid |
|---|---|
| Storage Instructions | For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles. |
| Storage Buffer | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS. |
