Junctophilin-2 Mouse Monoclonal Antibody [3-2]
cat.: M0407-20
Product Type: Mouse monoclonal IgG1, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IHC-P
Clonality: Monoclonal
Clone number: 3-2
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*PBS (pH7.4), 0.2% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 2ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 74 kDa
Isotype: IgG1
Immunogen: Synthetic peptide within Human Junctophilin-2 aa 1-50 / 696.
Positive control: Rat skeletal muscle tissue lysates, human skeletal muscle tissue, mouse skeletal muscle tissue, rat skeletal muscle tissue.
Subcellular location: Cell membrane.
Recommended Dilutions:
  WB
  IHC-P

1:1,000
1:1,000
Uniprot #: SwissProt: Q9BR39 Human | Q9ET78 Mouse | Q2PS20 Rat
Alternative names: FLJ40969 JP-2 JP2 Jph2 JPH2_HUMAN Junctophilin 2 Junctophilin type 2 Junctophilin-2 OTTHUMP00000031651 OTTHUMP00000031652
Images
M0407-20_1.jpg Fig1: Western blot analysis of Junctophilin-2 on rat skeletal muscle tissue lysates with Mouse anti-Junctophilin-2 antibody (M0407-20) at 1/1,000 dilution.

Lysates/proteins at 20 µg/Lane.

Predicted band size: 74 kDa
Observed band size: 70 kDa

Exposure time: 3 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 (M0407-20) at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Mouse IgG - HRP Secondary Antibody (HA1006) at 1/50,000 dilution was used for 1 hour at room temperature.
M0407-20_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human skeletal muscle tissue with Mouse anti-Junctophilin-2 antibody (M0407-20) 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 (M0407-20) 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.
M0407-20_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded mouse skeletal muscle tissue with Mouse anti-Junctophilin-2 antibody (M0407-20) 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 (M0407-20) 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.
M0407-20_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded rat skeletal muscle tissue with Mouse anti-Junctophilin-2 antibody (M0407-20) 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 (M0407-20) 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.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.