Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
---|---|
Species reactivity: | Human |
Applications: | IHC-P |
Clonality: | Monoclonal |
Clone number: | PD00-57 |
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: 35 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide. |
Positive control: | Human malignant melanoma tissue, human glioma tissue. |
Subcellular location: | Secreted, extracellular space, extracellular matrix, basement membrane. |
Recommended Dilutions:
IHC-P |
1:500-1:2,000 |
Uniprot #: | SwissProt: P09486 Human |
Alternative names: | AA517111 Basement membrane protein 40 Basement-membrane protein 40 BM 40 BM-40 BM40 Cysteine rich protein hm:zeh0062 MGC128090 OI17 ON Osteonectin Secreted acidic cystein rich glycoprotein Secreted protein acidic and cysteine rich Secreted protein acidic and rich in cysteine Secreted protein acidic cysteine rich (osteonectin) Secreted protein acidic cysteine rich SPARC SPRC SPRC_HUMAN |
Fig1:
Immunohistochemical analysis of paraffin-embedded human malignant melanoma tissue with Rabbit anti-SPARC antibody (HA721199) at 1/500 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 (HA721199) at 1/500 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. |
|
Fig2:
Immunohistochemical analysis of paraffin-embedded human glioma tissue with Rabbit anti-SPARC antibody (HA721199) at 1/2,000 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 (HA721199) 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. |