Von Willebrand Factor Recombinant Rabbit Monoclonal Antibody [JJ09-34]
cat.: ET1701-87
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse
Applications: WB, IHC-P, FC
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, bEnd.3.
Subcellular location: Secreted.
Recommended Dilutions:
  WB
  IHC-P
  FC

1:1,000-1:5,000
1:50-1:200
1:1,000
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
Images
ET1701-87_1.jpg 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;

3-8% 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.
ET1701-87_2.jpg 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.
ET1701-87_3.jpg Fig3: Flow cytometric analysis of bEnd.3 cells labeling Von Willebrand Factor.

Cells were fixed and permeabilized. Then stained with the primary antibody (ET1701-87, 1/1,000) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.