WB
Western blot analysis of TAZ on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (1/500) was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:200,000 dilution was used for 1 hour at room temperature. Positive control: Lane 1: Human placenta tissue lysate Lane 2: 293T cell lysateIHC
Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-TAZ antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (1/400) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.ICC/IF
ICC staining of TAZ in A549 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 10% negative goat serum for 15 minutes at room temperature. Cells were probed with the primary antibody (1/200) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 conjugate-Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).| Product Name | TAZ Rabbit Polyclonal Antibody |
|---|---|
| Antibody Type | Primary Antibodies |
| Immunogen | Recombinant protein within human TAZ aa 1-200 / 400. |
| Clonality | Polyclonal |
|---|---|
| Isotype | IgG |
| Host Species | Rabbit |
| Tested Applications | ICC/IFIHCWB |
| WB:1:500-1:1000 IHC:1:100-1:500 ICC:1:100-1:200 |
|
| Species Reactivity | HumanMouse |
| Concentration | 1mg/ml |
| Purification | Protein A |
| Gene Symbol | WWTR1 |
|---|---|
| Gene Synonyms | TAZ |
| Gene Full Name | WW domain containing transcription regulator 1 |
| Gene Summary | Enables transcription coactivator activity. Involved in several processes, including hippo signaling; positive regulation of cell differentiation; and regulation of signal transduction. Located in cytosol and nuclear body. [provided by Alliance of Genome Resources, Apr 2022] |
| Alternative Names | DKFZP586I1419 antibody FLJ27004 antibody FLJ45718 antibody OTTHUMP00000215994 antibody OTTHUMP00000215995 antibody OTTHUMP00000215996 antibody OTTHUMP00000216001 antibody TAZ antibody Transcriptional co activator with PDZ binding motif antibody Transcriptional coactivator with PDZ binding motif antibody DKFZP586I1419 antibody FLJ27004 antibody FLJ45718 antibody OTTHUMP00000215994 antibody OTTHUMP00000215995 antibody OTTHUMP00000215996 antibody OTTHUMP00000216001 antibody TAZ antibody Transcriptional co activator with PDZ binding motif antibody Transcriptional coactivator with PDZ binding motif antibody Transcriptional coactivator with PDZ-binding motif antibody WW domain containing transcription regulator 1 antibody WW domain containing transcription regulator protein 1 antibody WW domain-containing transcription regulator protein 1 antibody WWTR 1 antibody WWTR1 antibody WWTR1_HUMAN antibody |
| Molecular Weight(MW) | 44kDa |
| Cellular Localization | Cell membrane, Cytoplasm, Membrane, Nucleus. |
WB
Western blot analysis of TAZ on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (1/500) was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:200,000 dilution was used for 1 hour at room temperature. Positive control: Lane 1: Human placenta tissue lysate Lane 2: 293T cell lysate
IHC
Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-TAZ antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 20 minutes. The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (1/400) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
ICC/IF
ICC staining of TAZ in A549 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 10% negative goat serum for 15 minutes at room temperature. Cells were probed with the primary antibody (1/200) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 conjugate-Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).| Application Notes | WB:1:500-1:1000 IHC:1:100-1:500 ICC:1:100-1:200 |
|---|
| Form | Liquid |
|---|---|
| Storage Instructions | Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles. |
| Storage Buffer | 1*TBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide. |
