TRIM24 Recombinant Rabbit Monoclonal Antibody [JE64-31]
cat.: HA721052
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human
Applications: WB, IHC-P
Clonality: Monoclonal
Clone number: JE64-31
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 117 kDa
Isotype: IgG
Immunogen: Synthetic peptide within human TRIM24 aa 405-455/1,050.
Positive control: HepG2 cell lysate, HeLa cell lysate, human bladder carcinoma tissue, human breast carcinoma tissue, human thyroid tissue.
Subcellular location: Nucleus, Cytoplasm.
Recommended Dilutions:
  WB
  IHC-P

1:500
1:400-1:2,000
Uniprot #: SwissProt: O15164 Human
Alternative names: E3 ubiquitin protein ligase TRIM24 E3 ubiquitin-protein ligase Trim24 hTIF1 PTC6 RING finger protein 82 RNF82 TF1A TIF1 alpha TIF1 TIF1-alpha TIF1A TIF1A_HUMAN TIF1ALPHA Transcription intermediary factor 1-alpha Transcriptional intermediary factor 1 alpha Transcriptional intermediary factor 1 Trim24 Tripartite motif containing 24 Tripartite motif-containing protein 24
Images
HA721052_1.jpg Fig1: Western blot analysis of TRIM24 on different lysates with Rabbit anti-TRIM24 antibody at 1/500 dilution.

Lane 1: HepG2 cell lysate
Lane 2: HeLa cell lysate

Lysates/proteins at 10 µg/Lane.

Predicted band size: 117 kDa
Observed band size: 130 kDa

Exposure time: 2 minutes;

6 % SDS-PAGE gel.

Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody TRIM24 at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:300,000 dilution was used for 1 hour at room temperature.
HA721052_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human bladder carcinoma tissue with Rabbit anti-TRIM24 antibody at 1/2,000 dilution.

The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody TRIM24 at 1/2,000 dilution for 1 hour 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.
HA721052_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue with Rabbit anti-TRIM24 antibody at 1/400 dilution.

The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody TRIM24 at 1/400 dilution for 1 hour 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.
HA721052_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded human thyroid tissue with Rabbit anti-TRIM24 antibody at 1/1,000 dilution.

The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody TRIM24 at 1/1,000 dilution for 1 hour 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.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.