Phospho-PLK1 (T210) Recombinant Rabbit Monoclonal Antibody [JJ20-58]
cat.: ET1701-33
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse
Applications: WB, IF-Cell, IF-Tissue, FC, IHC-P
Clonality: Monoclonal
Clone number: JJ20-58
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: 68 kDa
Isotype: IgG
Immunogen: Synthetic phospho-peptide corresponding to residues surrounding Thr210 of Human PLK1 aa 181-230 / 603.
Positive control: Mouse thymus tissue, MCF-7.
Subcellular location: Nucleus, Chromosome, Cytoplasm, Midbody.
Recommended Dilutions:
  WB
  IF-Cell
  IF-Tissue
  FC
  IHC-P

1:500-1:1,000
1:10-1:50
1:10-1:50
1:10-1:50
1:200
Uniprot #: SwissProt: P53350 Human | Q07832 Mouse
Alternative names: Cell cycle regulated protein kinase PLK 1 PLK PLK-1 plk1 PLK1_HUMAN Polo like kinase 1 Polo-like kinase 1 Serine/threonine protein kinase 13 Serine/threonine protein kinase PLK1 Serine/threonine-protein kinase 13 Serine/threonine-protein kinase PLK1 STPK 13 STPK13
Images
ET1701-33_1.jpg Fig1: Immunohistochemical analysis of paraffin-embedded mouse thymus tissue with Rabbit anti-Phospho-PLK1 (T210) antibody (ET1701-33) at 1/200 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 (ET1701-33) at 1/200 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.
ET1701-33_2.jpg Fig2: Flow cytometric analysis of Phospho-PLK1 (T210) was done on MCF-7 cells. The cells were fixed, permeabilized and stained with the primary antibody (ET1701-33, 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”.