SOCS2 Recombinant Rabbit Monoclonal Antibody [JG36-86]
cat.: ET7108-40
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IF-Cell, IF-Tissue, IP, IHC-P
Clonality: Monoclonal
Clone number: JG36-86
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. 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: 22 kDa
Isotype: IgG
Immunogen: Recombinant protein within Human SOCS2 aa 1-198 / 198.
Positive control: SH-SY-5Y cell lysate, NIH/3T3 cell lysate, PC-12 cell lysate, mouse thymus tissue lysate, rat thymus tissue lysate, rat epididymis tissue, LOVO, PC-3M, SH-SY-5Y.
Subcellular location: Cytosol.
Recommended Dilutions:
  WB
  IF-Cell
  IP
  IHC-P

1:500-1:2,000
1:50-1:200
1:10-1:50
1:1,000
Uniprot #: SwissProt: O14508 Human | O35717 Mouse | O88582 Rat
Alternative names: CIS 2 CIS-2 CIS2 Cish 2 Cish2 Cytokine inducible SH2 protein 2 Cytokine-inducible SH2 protein 2 SOCS 2 SOCS-2 Socs2 SOCS2_HUMAN SSI 2 SSI-2 SSI2 STAT induced STAT inhibitor 2 STAT-induced STAT inhibitor 2 STATI 2 STATI2 Suppressor of cytokine signaling 2
Images
ET7108-40_1.jpg Fig1: Western blot analysis of SOCS2 on different lysates with Rabbit anti-SOCS2 antibody (ET7108-40) at 1/1,000 dilution.

Lane 1: SH-SY-5Y cell lysate
Lane 2: NIH/3T3 cell lysate
Lane 2: PC-12 cell lysate
Lane 3: Mouse thymus tissue lysate
Lane 4: Rat thymus tissue lysate

Lysates/proteins at 40 µg/Lane.

Predicted band size: 22 kDa
Observed band size: 22 kDa

Exposure time: 3 minutes 53 seconds;

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 (ET7108-40) 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.
ET7108-40_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded rat epididymis tissue with Rabbit anti-SOCS2 antibody (ET7108-40) 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 (ET7108-40) 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.
ET7108-40_3.jpg Fig3: Immunocytochemistry analysis of LOVO cells labeling SOCS2 with Rabbit anti-SOCS2 antibody (ET7108-40) at 1/50 dilution.

Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-SOCS2 antibody (ET7108-40) at 1/50 dilution in 2% negative goat serum overnight at 4 ℃.Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. Nuclear DNA was labelled in blue with DAPI.
ET7108-40_4.jpg Fig4: Immunocytochemistry analysis of PC-3M cells labeling SOCS2 with Rabbit anti-SOCS2 antibody (ET7108-40) at 1/50 dilution.

Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-SOCS2 antibody (ET7108-40) at 1/50 dilution in 2% negative goat serum overnight at 4 ℃.Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. Nuclear DNA was labelled in blue with DAPI.
ET7108-40_5.jpg Fig5: Immunocytochemistry analysis of SH-SY-5Y cells labeling SOCS2 with Rabbit anti-SOCS2 antibody (ET7108-40) at 1/50 dilution.

Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-SOCS2 antibody (ET7108-40) at 1/50 dilution in 2% negative goat serum overnight at 4 ℃.Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. Nuclear DNA was labelled in blue with DAPI.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.