Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse, Rat |
Applications: | WB, IHC-P, IHC-Fr, IF-Tissue |
Clonality: | Monoclonal |
Clone number: | PSH09-54 |
Form: | Liquid |
Storage condition: | Shipped at 4℃. Store at +4℃ short term (1-2 weeks). It is recommended to aliquot into single-use upon delivery. Store at -20℃ long term. |
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: 28 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide within human PHOS/PDC aa 36-69/246 |
Positive control: | Mouse eyeball tissue lysate, rat eyeball tissue lysate, mouse eyeball tissue, rat eyeball tissue. |
Subcellular location: | Cytoplasm, cytosol, Nucleus, Cell projection, cilium, photoreceptor outer segment, Photoreceptor inner segment, |
Recommended Dilutions:
WB IHC-P IHC-Fr IF-Tissue |
1:2,000 1:1,000-1:8,000 1:500 1:200-1:2,000 |
Uniprot #: | SwissProt: P20941 Human | Q9QW08 Mouse | P20942 Rat |
Alternative names: | 33 kDa phototransducing protein MEKA protein pdc PHD PHOS_HUMAN Phosducin Protein MEKA |
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Fig1:
Western blot analysis of PHOS / PDC on different lysates with Rabbit anti-PHOS / PDC antibody (HA723116) at 1/2,000 dilution. Lane 1: mouse eyeball tissue lysate (40 µg/Lane) Lane 2: mouse liver tissue lysate (negative) (40 µg/Lane) Lane 3: rat eyeball tissue lysate (40 µg/Lane) Lane 4: rat liver tissue lysate (negative) (40 µg/Lane) Predicted band size: 28 kDa Observed band size: 33 kDa Exposure time: 3 minutes ; ECL: K1802; 4-20% 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 (HA723116) at 1/2,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature. |
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Fig2:
Immunohistochemical analysis of paraffin-embedded mouse eyeball tissue with Rabbit anti-PHOS / PDC antibody (HA723116) at 1/1,000 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 (HA723116) 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. |
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Fig3:
Immunohistochemical analysis of paraffin-embedded rat eyeball tissue with Rabbit anti-PHOS / PDC antibody (HA723116) 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 (HA723116) 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. |
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Fig4:
Immunofluorescence analysis of frozen mouse eyeball tissue with Rabbit anti-PHOS / PDC antibody (HA723116) at 1/500 dilution. The section was not undergone antigen retrieval. The tissues were blocked in 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (HA723116, green) at 1/500 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue). |