NR1D1 Recombinant Rabbit Monoclonal Antibody [JU34-31]
cat.: ET7106-92
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IHC-P
Clonality: Monoclonal
Clone number: JU34-31
Form: Liquid
Storage condition: Shipped at 4℃. Store at +4℃ short term (1-2 weeks). Store at -20℃ long term.
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: 67 kDa
Isotype: IgG
Immunogen: Recombinant protein within Human NR1D1 aa 510-614 / 614.
Positive control: HepG2 cell lysate, SiHa cell lysate, human colon cancer tissue, mouse fallopian tube tissue, mouse kidney tissue, mouse brain tissue, rat brain tissue.
Subcellular location: Nucleus, Cytoplasm, Cell projection, dendrite, dendritic spine.
Recommended Dilutions:
  WB
  IHC-P

1:500-1:1,000
1:200
Uniprot #: SwissProt: P20393 Human | Q3UV55 Mouse | Q63503 Rat
Alternative names: EAR-1 EAR1 ERBA-related 1 hRev Nr1d1 NR1D1_HUMAN Nuclear receptor Rev ErbA alpha Nuclear receptor subfamily 1 group D member 1 Rev erbAalpha Rev erbalpha Rev-erbA-alpha Rev-ErbAalpha Reverba THRA1 THRAL Thyroid hormone receptor, alpha like Thyroid hormone receptor, alpha-1- like V-erbA-related protein 1
Images
ET7106-92_1.jpg Fig1: Immunohistochemical analysis of paraffin-embedded human colon cancer tissue with Rabbit anti-NR1D1 antibody (ET7106-92) at 1/200 dilution.

The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) 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 (ET7106-92) at 1/200 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.
ET7106-92_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded mouse fallopian tube tissue with Rabbit anti-NR1D1 antibody (ET7106-92) at 1/200 dilution.

The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) 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 (ET7106-92) at 1/200 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.
ET7106-92_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded mouse kidney tissue with Rabbit anti-NR1D1 antibody (ET7106-92) at 1/200 dilution.

The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) 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 (ET7106-92) at 1/200 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.
ET7106-92_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded mouse brain tissue with Rabbit anti-NR1D1 antibody (ET7106-92) at 1/200 dilution.

The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) 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 (ET7106-92) at 1/200 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.
ET7106-92_5.jpg Fig5: Immunohistochemical analysis of paraffin-embedded rat brain tissue with Rabbit anti-NR1D1 antibody (ET7106-92) at 1/200 dilution.

The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) 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 (ET7106-92) at 1/200 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”.