Product Type: | Rabbit polyclonal IgG, primary antibodies |
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Species reactivity: | Human |
Applications: | WB, IF-Cell, IHC-P, FC |
Clonality: | Polyclonal |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | PBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Immunogen affinity purified. |
Molecular weight: | Predicted band size: 97 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide within human IL-12RB2 aa 751-800. |
Positive control: | HepG2 cell lysate, 293T cell lysate, Hela, human placenta tissue, THP-1. |
Subcellular location: | Membrane. |
Recommended Dilutions:
WB IF-Cell IHC-P FC |
1:500 1:200 1:600 1:500-1:1,000 |
Uniprot #: | SwissProt: Q99665 Human |
Alternative names: | I12R2_HUMAN IL-12 receptor subunit beta-2 IL-12R subunit beta-2 IL-12R-beta-2 IL-12RB2 IL12 receptor beta 2 IL12R beta2 IL12RB2 Interleukin 12 receptor beta 2 Interleukin 12 receptor beta 2 chain Interleukin-12 receptor subunit beta-2 RP11 102M16.1 |
Fig1:
Western blot analysis of IL-12RB2 on different lysates with Rabbit anti-IL-12RB2 antibody (HA500320) at 1/2,000 dilution. Lane 1: HepG2 cell lysate Lane 2: 293T cell lysate Lysates/proteins at 10 µg/Lane. Predicted band size: 97 kDa Observed band size: 97 kDa Exposure time: 2 minutes; 8% 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 (HA500320) at 1/2,000 dilution was used in 5% NFDM/TBST 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. |
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Fig2:
Immunocytochemistry analysis of Hela cells labeling IL-12RB2 with Rabbit anti-IL-12RB2 antibody (HA500320) at 1/200 dilution. Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-IL-12RB2 antibody (HA500320) at 1/200 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. |
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Fig3:
Immunohistochemical analysis of paraffin-embedded human placenta tissue with Rabbit anti-IL-12RB2 antibody (HA500320) at 1/600 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 (HA500320) at 1/600 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. |
Fig4:
Flow cytometric analysis of THP-1 cells labeling IL-12RB2. Cells were washed twice with cold PBS and resuspend. Then stained with the primary antibody (HA500320, 1ug/ml) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a Alexa Fluor® 488 conjugate-Goat anti-Rabbit IgG Secondary antibody at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black). |