LPP Recombinant Rabbit Monoclonal Antibody [JE55-29]
cat.: ET7111-02
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IHC-P
Clonality: Monoclonal
Clone number: JE55-29
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: 66 kDa.
Isotype: IgG
Immunogen: Recombinant protein within Human LPP aa 1-140 / 612.
Positive control: Human skin tissue lysate, Daudi cell lysate, rat skin tissue lysate, mouse smooth muscle tissue lysate, rat bladder tissue, human kidney intestine tissue, human small intestine tissue.
Subcellular location: Nucleus, cell membrane, cytoplasm, cell junction.
Recommended Dilutions:
  WB
  IHC-P

1:500-1:2,000
1:50-1:200
Uniprot #: SwissProt: Q93052 Human | Q8BFW7 Mouse | Q5XI07 Rat
Alternative names: DKFZp779O0231 FLJ30652 FLJ41512 LIM domain containing preferred translocation partner in lipoma LIM domain-containing preferred translocation partner in lipoma LIM protein Lipoma preferred partner Lipoma-preferred partner lpp LPP_HUMAN
Images
ET7111-02_1.jpg Fig1: Western blot analysis of LPP on different lysates with Rabbit anti-LPP antibody (ET7111-02) at 1/500 dilution.

Lane 1: Human skin tissue lysate
Lane 2: Daudi cell lysate(10 µg/Lane)

Lysates/proteins at 20 µg/Lane.

Predicted band size: 66 kDa
Observed band size: 75 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 (ET7111-02) 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 1:5,000 dilution was used for 1 hour at room temperature.
ET7111-02_2.jpg Fig2: Western blot analysis of LPP on different lysates with Rabbit anti-LPP antibody (ET7111-02) at 1/500 dilution.

Lane 1: Rat skin tissue lysate
Lane 2: Mouse smooth muscle tissue lysate

Lysates/proteins at 20 µg/Lane.

Predicted band size: 66 kDa
Observed band size: 75 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 (ET7111-02) 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 1:5,000 dilution was used for 1 hour at room temperature.
ET7111-02_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded rat bladder tissue with Rabbit anti-LPP antibody (ET7111-02) at 1/400 dilution.

The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 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 (ET7111-02) 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.
ET7111-02_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded human kidney intestine tissue with Rabbit anti-LPP antibody (ET7111-02) at 1/50 dilution.

The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 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 (ET7111-02) at 1/50 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.
ET7111-02_5.jpg Fig5: Immunohistochemical analysis of paraffin-embedded human small intestine tissue with Rabbit anti-LPP antibody (ET7111-02) at 1/50 dilution.

The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 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 (ET7111-02) at 1/50 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”.