MEKK2 Recombinant Rabbit Monoclonal Antibody [SC68-02]
cat.: ET1610-70
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IF-Cell, IHC-P, IP, FC
Clonality: Monoclonal
Clone number: SC68-02
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: 70 kDa
Isotype: IgG
Immunogen: Synthetic peptide within Human MEKK2 aa 1-47 / 619.
Positive control: SW480, MCF-7, HepG2,HEK293A, MBMEC, mouse brain tissue, human breast carcinoma tissue, rat brain tissue.
Subcellular location: Cytoplasm, Nucleus.
Recommended Dilutions:
  WB
  IF-Cell
  IHC-P
  FC

1:1,000-1:2,000
1:50-1:200
1:50-1:200
1:50-1:100
Uniprot #: SwissProt: Q9Y2U5 Human | Q61083 Mouse
Unigene: 213212 Rat
Alternative names: M3K2_HUMAN Map3k2 MAPK/ERK kinase kinase 2 MEK kinase 2 MEKK 2 MEKK2b Mitogen activated protein kinase kinase kinase 2 Mitogen-activated protein kinase kinase kinase 2
Images
ET1610-70_1.jpg Fig1: All lanes: Western blot analysis of MEKK2 with anti-MEKK2 antibody [SC68-02] (ET1610-70) at 1:1,000 dilution.
Lane 1: Wild-type HEK293A whole cell lysate (20 µg).
Lane 2: MEKK2 knockout HEK293A whole cell lysate (20 µg).
Lane 3: Wild-type MBMEC whole cell lysate (20 µg).
Lane 4: MEKK2 knockout MBMEC whole cell lysate (20 µg).

ET1610-70 was shown to specifically react with MEKK2 in Wild-type HEK293A and Wild-type MBMEC cells. No band was observed when MEKK2 knockout samples were tested. Wild-type and MEKK2 knockout samples were subjected to SDS-PAGE. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM in TBST for 1 hour at room temperature. The primary Anti-MEKK2 antibody (ET1610-70, 1/1,000) and Anti-β-actin antibody (R1207-1, 1/1,000) were used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG H&L (HRP) Secondary Antibody (HA1001) at 1:200,000 dilution was used for 1 hour at room temperature.
ET1610-70_2.jpg Fig2: Western blot analysis of MEKK2 on different lysates using anti-MEKK2 antibody at 1/1,000 dilution.
Positive control:
Lane 1: HepG2
Lane 2: Rat brain
Lane 3: SW480
ET1610-70_3.jpg Fig3: ICC staining MEKK2 in HepG2 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
ET1610-70_4.jpg Fig4: ICC staining MEKK2 in MCF-7 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
ET1610-70_5.jpg Fig5: ICC staining MEKK2 in SW480 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
ET1610-70_6.jpg Fig6: Immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue using anti-MEKK2 antibody. Counter stained with hematoxylin.
ET1610-70_7.jpg Fig7: Immunohistochemical analysis of paraffin-embedded mouse brain tissue using anti-MEKK2 antibody. Counter stained with hematoxylin.
ET1610-70_8.jpg Fig8: Flow cytometric analysis of HepG2 cells with MEKK2 antibody at 1/50 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black). Alexa Fluor 488-conjugated goat anti rabbit IgG was used as the secondary antibody.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.