Product Type: | Recombinant Mouse monoclonal IgG1, primary antibodies |
---|---|
Species reactivity: | Zebrafish |
Applications: | IHC-P, IF-Tissue |
Clonality: | Monoclonal |
Clone number: | A3B10-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: 94.5 kDa |
Isotype: | IgG1 |
Immunogen: | Recombinant protein within zebrafish ddx24 aa 562-819 / 832. |
Positive control: | Zebrafish tissue. |
Subcellular location: | Nucleolus. |
Recommended Dilutions:
IHC-P IF-Tissue |
1:1,000 1:50 |
Uniprot #: | SwissProt: A0A0R4IA19 Zebrafish |
Alternative names: | DEAD (Asp-Glu-Ala-Asp) box helicase 24 ddx24 |
Fig1:
Immunofluorescence analysis of paraffin-embedded zebrafish (head) tissue labeling ddx24 with Mouse anti-ddx24 antibody (HA601183) at 1/50 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 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (HA601183, green) at 1/50 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Mouse IgG H&L (iFluor™ 488, HA1125) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue). |
|
Fig2:
Immunofluorescence analysis of paraffin-embedded zebrafish (tail) tissue labeling ddx24 with Mouse anti-ddx24 antibody (HA601183) at 1/50 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 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (HA601183, green) at 1/50 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Mouse IgG H&L (iFluor™ 488, HA1125) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue). |
|
Fig3:
Immunohistochemical analysis of paraffin-embedded zebrafish tissue with Mouse anti-ddx24 antibody (HA601183) 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 (HA601183) 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. |