MUC16 Recombinant Rabbit Monoclonal Antibody [SN0715]
cat.: ET1611-73
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human
Applications: WB, IF-Cell, IF-Tissue, IHC-P, FC
Clonality: Monoclonal
Clone number: SN0715
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: 1519 kDa
Isotype: IgG
Immunogen: Recombinant protein within Human MUC16 aa 12331-12339 / 14,507.
Positive control: SK-OV-3 cell lysate, NIH:OVCAR-3 cell lysate, HepG2, Hela, SKOV-3, human endometrium tissue.
Subcellular location: Cell membrane, extracellular space.
Recommended Dilutions:
  WB
  IF-Cell
  IF-Tissue
  IHC-P
  FC
1:1,000
1:100-1:500
1:200
1:1,000
1:50-1:100
Uniprot #: SwissProt: Q8WXI7 Human
Alternative names: CA 125 CA-125 CA125 CA125 ovarian cancer antigen Cancer antigen 125 FLJ14303 MUC 16 MUC-16 MUC16 MUC16_HUMAN Mucin 16 Mucin 16 cell surface associated Mucin-16 Mucin16 Ovarian cancer related tumor marker CA125 Ovarian cancer-related tumor marker CA125 Ovarian carcinoma antigen CA125
Images
ET1611-73_1.jpg Fig1: Western blot analysis of MUC16 on different lysates with Rabbit anti-MUC16 antibody (ET1611-73) at 1/1,000 dilution.

Lane 1: SK-OV-3 cell lysate (negative) (20 µg/Lane)
Lane 2: NIH:OVCAR-3 cell lysate (20 µg/Lane)

Predicted band size: 1519 kDa

Exposure time: 1 minutes; ECL: K1801;
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 (ET1611-73) at 1/1,000 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.
ET1611-73_2.jpg Fig2: ICC staining of MUC16 in HepG2 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1611-73, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).
ET1611-73_3.jpg Fig3: ICC staining of MUC16 in Hela cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1611-73, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).
ET1611-73_4.jpg Fig4: ICC staining of MUC16 in SKOV-3 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 1% Blocker BSA for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1611-73, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).
ET1611-73_5.jpg Fig5: Immunohistochemical analysis of paraffin-embedded human endometrium tissue with Rabbit anti-MUC16 antibody (ET1611-73) 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 (ET1611-73) 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.
ET1611-73_6.jpg Fig6: Flow cytometric analysis of MUC16 was done on Hela cells. The cells were fixed, permeabilized and stained with the primary antibody (ET1611-73, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.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”.