AGO3 Recombinant Rabbit Monoclonal Antibody [JJ201-07]
cat.: ET1701-26
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IF-Cell, IF-Tissue, IHC-P, FC
Clonality: Monoclonal
Clone number: JJ201-07
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: 97 kDa
Isotype: IgG
Immunogen: Recombinant protein within human EIF2C3/ Argonaute 3 aa 689-860/860.
Positive control: HeLa cell lysate, C6 cell lysate, N2A, SHG-44, F9, NCCIT, rat spinal cord tissue, rat brain tissue, mouse brain tissue, rat testis tissue.
Subcellular location: Cytoplasm,Nucleus.
Recommended Dilutions:
  WB
  IF-Cell
  IF-Tissue
  IHC-P
  FC

1:1,000
1:100-1:500
1:100-1:500
1:50-1:200
1:50-1:100
Uniprot #: SwissProt: Q9H9G7 Human | Q8CJF9 Mouse
Unigene: 92025 Rat
Alternative names: 5730550L01Rik Ago 3 Ago3 AGO3_HUMAN argonaute 3 Argonaute3 eIF 2C 3 eIF-2C 3 eIF2C 3 Eif2c3 EIF2C3 protein Eukaryotic translation initiation factor 2C 3 Eukaryotic translation initiation factor 2C3 FLJ12765 hAgo3 MGC86946 Protein argonaute-3
Images
ET1701-26_1.jpg Fig1: Western blot analysis of AGO3 on different lysates with Rabbit anti-AGO3 antibody (ET1701-26) at 1/1,000 dilution.

Lane 1: HeLa cell lysate
Lane 2: C6 cell lysate

Lysates/proteins at 20 µg/Lane.

Predicted band size: 97 kDa
Observed band size: 97 kDa

Exposure time: 3 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 (ET1701-26) 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.
ET1701-26_2.jpg Fig2: ICC staining AGO3 in N2A cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
ET1701-26_3.jpg Fig3: ICC staining AGO3 in SHG-44 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
ET1701-26_4.jpg Fig4: ICC staining AGO3 in F9 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
ET1701-26_5.jpg Fig5: ICC staining AGO3 in NCCIT cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
ET1701-26_6.jpg Fig6: Immunohistochemical analysis of paraffin-embedded rat spinal cord tissue using anti-AGO3 antibody. Counter stained with hematoxylin.
ET1701-26_7.jpg Fig7: Immunohistochemical analysis of paraffin-embedded rat brain tissue using anti-AGO3 antibody. Counter stained with hematoxylin.
ET1701-26_8.jpg Fig8: Immunohistochemical analysis of paraffin-embedded mouse brain tissue using anti-AGO3 antibody. Counter stained with hematoxylin.
ET1701-26_9.jpg Fig9: Immunohistochemical analysis of paraffin-embedded rat testis tissue using anti-AGO3 antibody. Counter stained with hematoxylin.
ET1701-26_10.jpg Fig10: Flow cytometric analysis of N2A cells with AGO3 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”.