IL-12RB1 Rabbit Polyclonal Antibody
cat.: HA500321
Product Type: Rabbit polyclonal IgG, primary antibodies
Species reactivity: Human
Applications: WB, IHC-P
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: 73 kDa
Isotype: IgG
Immunogen: Synthetic peptide within human IL-12RB1 aa 51-100.
Positive control: 293T cell lysates, human placenta tissue.
Subcellular location: Membrane.
Recommended Dilutions:
  WB
  IHC-P

1:500
1:600
Uniprot #: SwissProt: P42701 Human
Alternative names: CD212 cluster of differentiation 212 I12R1_HUMAN IL-12 receptor beta component IL-12 receptor subunit beta-1 IL-12R subunit beta-1 IL-12R-beta-1 IL-12RB1 IL12 receptor beta component IL12RB Il12rb1 IMD3 IMD30 Interleukin 12 receptor beta 1 chain Interleukin 12 receptor subunit beta 1 Interleukin-12 receptor subunit beta-1 MGC34454
Images
HA500321_1.jpg Fig1: Western blot analysis of IL-12RB1 on 293T cell lysates with Rabbit anti-IL-12RB1 antibody (HA500321) at 1/500 dilution.

Lysates/proteins at 10 µg/Lane.

Predicted band size: 73 kDa
Observed band size: 65 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 (HA500321) at 1/500 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.
HA500321_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human placenta tissue with Rabbit anti-IL-12RB1 antibody (HA500321) 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 (HA500321) 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.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.