pan Cytokeratin Recombinant Mouse Monoclonal Antibody [PD00-15]
cat.: HA601094
Product Type: Recombinant Mouse monoclonal IgG1, primary antibodies
Species reactivity: Human
Applications: IHC-P, IF-Cell, FC, mIHC
Clonality: Monoclonal
Clone number: PD00-15
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.
Isotype: IgG1
Immunogen: Recognizes human cytokeratins 4, 5, 6, 8, 10, 13, and 18.
Positive control: Human skin tissue, human breast tissue, human small intestine tissue, MCF-7, human pancreatic carcinoma.
Subcellular location: Cytoplasm.
Recommended Dilutions:
  IHC-P
  IF-Cell
  FC
  mIHC
1:500-1:1,000
1:50
1:500-1:1,000
1:3,000
Uniprot #: SwissProt: Q01546 Human | Q7Z794 Human
Alternative names: pan ck pan-ck panck
Images
HA601094_1.jpg Fig1: Immunohistochemical analysis of paraffin-embedded human skin tissue with Mouse anti-pan Cytokeratin antibody (HA601094) 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 (HA601094) 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.
HA601094_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human breast tissue with Mouse anti-pan Cytokeratin antibody (HA601094) 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 (HA601094) 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.
HA601094_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded human small intestine tissue with Mouse anti-pan Cytokeratin antibody (HA601094) at 1/500 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 (HA601094) at 1/500 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.
HA601094_4.jpg Fig4: Immunocytochemistry analysis of MCF7 cells labeling pan Cytokeratin with Mouse anti-pan Cytokeratin antibody (HA601094) at 1/50 dilution.

Cells were fixed in 4% paraformaldehyde for 30 minutes, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes, and then blocked with 2% BSA for 30 minutes at room temperature. Cells were then incubated with Mouse anti-pan Cytokeratin antibody (HA601094) at 1/50 dilution in 2% BSA overnight at 4 ℃. Goat Anti-Mouse IgG H&L (iFluor™ 488, HA1125) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.
HA601094_5.jpg Fig5: Fluorescence multiplex immunohistochemical analysis of the human pancreatic carcinoma (Formalin/PFA-fixed paraffin-embedded sections). Panel A: the merged image of anti-CD68 (EM1901-95, green), anti-CD163 (ET1704-43, red) and anti-PanCK (HA601094, violet) on human pancreatic carcinoma. Panel B: anti- CD68 stained on M1 macrophages. Panel C: anti-CD163 stained on M2 macrophages cells. Panel D: anti-panCK stained on cancer cells. HRP Conjugated UltraPolymer Goat Polyclonal Antibody HA1119/HA1120 was used as a secondary antibody. The immunostaining was performed with the Sequential Immuno-staining Kit (IRISKit™MH010101, www.luminiris.cn). The section was incubated in three rounds of staining: in the order of EM1901-95 (1/3,000 dilution), ET1704-43 (1/3,000 dilution), and HA601094 (1/3,000 dilution) for 20 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 30 mins at 95℃. DAPI (blue) was used as a nuclear counter stain. Image acquisition was performed with Nikon ECLIPSE Ni-E microscope.
HA601094_6.jpg Fig6: Flow cytometric analysis of MCF7 cells labeling pan Cytokeratin.

Cells were fixed and permeabilized.Then stained with the primary antibody (HA601094, 1ug/ml) (red) compared with Mouse IgG1 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-Mouse IgG Secondary antibody (HA1125) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
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