Product Type: | Rabbit polyclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse |
Applications: | WB, IHC-P |
Clonality: | Polyclonal |
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: | 2.22ug/ul |
Purification: | Immunogen affinity purified. |
Molecular weight: | Predicted band size: 63.5 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide within human FZD2 aa 301-327 (Extracellular domain). |
Positive control: | 293 cell lysate, HepG2 cell lysate, Hela cell lysate, mouse heart tissue. |
Subcellular location: | Cell membrane. |
Recommended Dilutions:
WB IHC-P |
1:1,000 1:600 |
Uniprot #: | SwissProt: Q14332 Human | Q9JIP6 Mouse |
Alternative names: | Frizzled homolog 2 Frizzled-2 Frizzled2 Fz 2 Fz-2 Fz2 FZD 2 FZD2 FZD2_HUMAN FzE 2 FzE2 hFz 2 hFz2 Mfz10 |
Fig1:
Western blot analysis of FZD2 on different lysates with Rabbit anti-FZD2 antibody (HA500406) at 1/1,000 dilution. Lane 1: 293 cell lysate Lane 2: HepG2 cell lysate Lane 3: Hela cell lysate Lysates/proteins at 10 µg/Lane. Predicted band size: 63.5 kDa Observed band size: 85 kDa Exposure time: 2 minutes; 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 (HA500406) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:100,000 dilution was used for 1 hour at room temperature. |
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Fig2:
Immunohistochemical analysis of paraffin-embedded mouse heart tissue with Rabbit anti-FZD2 antibody (HA500406) at 1/600 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 (HA500406) at 1/600 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. |