PREPL Recombinant Rabbit Monoclonal Antibody [JE65-64]
cat.: HA721069
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IHC-P
Clonality: Monoclonal
Clone number: JE65-64
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: 84 kDa
Isotype: IgG
Immunogen: Recombinant protein within human PREPL aa 621-720/727.
Positive control: NIH/3T3 cell lysates, PC-12 cell lysates, rat hippocampus tissue, rat brain tissue, mouse hippocampus tissue, mouse brain tissue.
Subcellular location: Cytoskeleton, Nucleus, cytosol, trans-Golgi network, Golgi apparatus.
Recommended Dilutions:
  WB
  IHC-P

1:500
1:400
Uniprot #: SwissProt: Q4J6C6 Human | Q8C167 Mouse | Q5HZA6 Rat
Alternative names: PPCEL_HUMAN prepl Prolyl endopeptidase-like Prolylendopeptidase-like putative prolyl oligopeptidase
Images
HA721069_1.jpg Fig1: Western blot analysis of PREPL on NIH/3T3 cell lysates with Rabbit anti-PREPL antibody (HA721069) at 1/500 dilution.

Lysates/proteins at 10 µg/Lane.

Predicted band size: 84 kDa
Observed band size: 70 kDa

Exposure time: 2 minutes;

10% 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 (HA721069) 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 1:300,000 dilution was used for 1 hour at room temperature.
HA721069_2.jpg Fig2: Western blot analysis of PREPL on PC-12 cell lysates with Rabbit anti-PREPL antibody (HA721069) at 1/500 dilution.

Lysates/proteins at 10 µg/Lane.

Predicted band size: 84 kDa
Observed band size: 70 kDa

Exposure time: 2 minutes;

10% 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 (HA721069) 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 1:300,000 dilution was used for 1 hour at room temperature.
HA721069_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded rat hippocampus tissue with Rabbit anti-PREPL antibody (HA721069) at 1/400 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 (HA721069) at 1/400 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.
HA721069_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded rat brain tissue with Rabbit anti-PREPL antibody (HA721069) at 1/400 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 (HA721069) at 1/400 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.
HA721069_5.jpg Fig5: Immunohistochemical analysis of paraffin-embedded mouse hippocampus tissue with Rabbit anti-PREPL antibody (HA721069) at 1/400 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 (HA721069) at 1/400 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.
HA721069_6.jpg Fig6: Immunohistochemical analysis of paraffin-embedded mouse brain tissue with Rabbit anti-PREPL antibody (HA721069) at 1/400 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 (HA721069) at 1/400 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”.