Noxa Recombinant Rabbit Monoclonal Antibody [JA30-03]
cat.: ET1704-35
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IHC-P
Clonality: Monoclonal
Clone number: JA30-03
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. 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: 6 kDa
Isotype: IgG
Immunogen: Synthetic peptide within Human Noxa aa 5-54 / 54.
Positive control: Human spleen tissue, human liver tissue, Jurkat, mouse lung tissue, rat lung tissue.
Subcellular location: Mitochondrion.
Recommended Dilutions:
  WB
  IHC-P

1:500
1:8,000
Uniprot #: SwissProt: Q13794 Human | Q9JM54 Mouse | Q5U777 Rat
Alternative names: Adult T cell leukemia derived PMA responsive APR APR_HUMAN ATL-derived Immediate early response protein APR Immediate-early-response protein APR NOXA Phorbol 12 myristate 13 acetate induced protein 1 Phorbol-12-myristate-13-acetate-induced protein 1 PMA induced protein 1 PMA-induced protein 1 PMA-responsive gene Pmaip1 Protein Noxa
Images
ET1704-35_1.jpg Fig1: Immunohistochemical analysis of paraffin-embedded mouse lung tissue with Rabbit anti-Noxa antibody (ET1704-35) at 1/8,000 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 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 (ET1704-35) at 1/8,000 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.
ET1704-35_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded rat lung tissue with Rabbit anti-Noxa antibody (ET1704-35) at 1/8,000 dilution.

The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 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 (ET1704-35) at 1/8,000 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”.