SUMO4 Recombinant Rabbit Monoclonal Antibody [JJ085-01]
cat.: ET1701-8
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Rat, Mouse
Applications: WB, IF-Cell, IF-Tissue, FC, IP
Clonality: Monoclonal
Clone number: JJ085-01
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: 11 kDa
Isotype: IgG
Immunogen: Recombinant protein within Human SUMO4 aa1-105 / 95.
Positive control: 293T cell lysate, Jurkat cell lysate, 293, MCF-7, HepG2, RH-35.
Subcellular location: Nucleus, SUMO ligase complex.
Recommended Dilutions:
  WB
  FC
  IF-Cell
  IF-Tissue
  IP

1:1,000-1:2,000
1:50-1:100
1:100-1:500
1:100-1:500
Use at an assay dependent concentration.
Uniprot #: SwissProt: Q6EEV6 Human | P61957 Mouse | P61959 Rat
Alternative names: dJ281H8.4 IDDM5 Small ubiquitin like modifier 4 protein Small ubiquitin-like protein 4 Small ubiquitin-related modifier 4 SMT3 suppressor of mif two 3 homolog 2 SMT3 suppressor of mif two 3 homolog 4 (S. cerevisiae) SMT3H4 SUMO 4 SUMO-4 SUMO4 SUMO4_HUMAN
Images
ET1701-8_1.jpg Fig1: Western blot analysis of SUMO4 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (ET1701-8, 1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:200,000 dilution was used for 1 hour at room temperature.
Positive control:
Lane 1: 293T cell lysate
Lane 2: Jurkat cell lysate
ET1701-8_2.jpg Fig2: ICC staining of SUMO4 in 293 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 10% negative goat serum for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1701-8, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 conjugate-Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).
ET1701-8_3.jpg Fig3: ICC staining of SUMO4 in MCF-7 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 10% negative goat serum for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1701-8, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 conjugate-Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).
ET1701-8_4.jpg Fig4: ICC staining of SUMO4 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 10% negative goat serum for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1701-8, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 conjugate-Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).
ET1701-8_5.jpg Fig5: ICC staining of SUMO4 in RH-35 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 10% negative goat serum for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1701-8, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 conjugate-Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).
ET1701-8_6.jpg Fig6: Flow cytometric analysis of SUMO4 was done on 293 cells. The cells were fixed, permeabilized and stained with the primary antibody (ET1701-8, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor®488 conjugate-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”.