Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse |
Applications: | WB, IHC-P |
Clonality: | Monoclonal |
Clone number: | JJ09-34 |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Protein A affinity purified. |
Molecular weight: | Predicted band size: 309 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein within Human Von Willebrand Factor aa 1170-1320 / 2813. |
Positive control: | BEnd.3 cell lysate, human lung tissue lysate, mouse lung tissue lysate, mouse liver tissue lysate, human tonsil tissue. |
Subcellular location: | Secreted. |
Recommended Dilutions:
WB IHC-P |
1:1,000-1:5,000 1:50-1:200 |
Uniprot #: | SwissProt: P04275 Human | Q8CIZ8 Mouse |
Alternative names: | Coagulation factor VIII Coagulation factor VIII VWF F8VWF Factor VIII related antigen von Willebrand antigen 2 von Willebrand antigen II Von Willebrand disease VWD vWF VWF_HUMAN |
Fig1:
Western blot analysis of Von Willebrand Factor on different lysates with Rabbit anti-Von Willebrand Factor antibody (ET1701-87) at 1/1,000 dilution. Lane 1: bEnd.3 cell lysate Lane 2: Human lung tissue lysate Lane 3: Mouse lung tissue lysate Lane 4: Mouse liver tissue lysate Lysates/proteins at 20 µg/Lane. Predicted band size: 309 kDa Observed band size: 309 kDa Exposure time: 5 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 (ET1701-87) 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 1/50,000 dilution was used for 1 hour at room temperature. |
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Fig2:
Immunohistochemical analysis of paraffin-embedded human tonsil tissue with Rabbit anti-Von Willebrand Factor antibody (ET1701-87) at 1/400 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 (ET1701-87) at 1/400 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. |