BRCA1 Recombinant Mouse Monoclonal Antibody [A7E3-R]
cat.: HA601304
Product Type: Recombinant Mouse monoclonal IgG1, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: IHC-P
Clonality: Monoclonal
Clone number: A7E3-R
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 208 kDa
Isotype: IgG1
Immunogen: Recombinant protein within Human BRCA1 aa 1-200 / 1,863.
Positive control: Human brain tissue, human breast tissue, human breast cancer tissue, human skin tissue, mouse brian tissue, rat brian tissue.
Subcellular location: Cytoplasm, Nucleus, Chromosome.
Recommended Dilutions:
  IHC-P

1:1,000-1:5,000
Uniprot #: SwissProt: P38398 Human | P48754 Mouse | O54952 Rat
Alternative names: BRCA 1 BRCA1 BRCA1 DNA repair associated BRCA1/BRCA2 containing complex subunit 1 BRCA1/BRCA2-containing complex, subunit 1 BRCA1_HUMAN BRCAI BRCC 1 BRCC1 Breast and ovarian cancer susceptibility protein 1 Breast Cancer 1 Breast Cancer 1 Early Onset Breast cancer type 1 susceptibility protein BROVCA1 FANCS IRIS PNCA4 PPP1R53 Protein phosphatase 1 regulatory subunit 53 PSCP RING finger protein 53 RNF53
Images
HA601304_1.jpg Fig1: Immunohistochemical analysis of paraffin-embedded human brain tissue with Mouse anti-BRCA1 antibody (HA601304) 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 (HA601304) 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.
HA601304_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human breast tissue with Mouse anti-BRCA1 antibody (HA601304) 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 (HA601304) 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.
HA601304_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded human breast cancer tissue with Mouse anti-BRCA1 antibody (HA601304) 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 (HA601304) 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.
HA601304_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded human skin tissue with Mouse anti-BRCA1 antibody (HA601304) 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 (HA601304) 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.
HA601304_5.jpg Fig5: Immunohistochemical analysis of paraffin-embedded mouse brian tissue with Mouse anti-BRCA1 antibody (HA601304) at 1/5,000 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 (HA601304) at 1/5,000 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.
HA601304_6.jpg Fig6: Immunohistochemical analysis of paraffin-embedded rat brian tissue with Mouse anti-BRCA1 antibody (HA601304) at 1/5,000 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 (HA601304) at 1/5,000 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”.