Lrp2 / Megalin Recombinant Rabbit Monoclonal Antibody [PSH02-91]
cat.: HA721910
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human
Applications: IHC-P, IF-Tissue, WB
Clonality: Monoclonal
Clone number: PSH02-91
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 522 kDa
Isotype: IgG
Immunogen: Synthetic peptide within human Lrp2 aa 2,500-3,200 / 4,655.
Positive control: Human kidney tissue lysates, human kidney tissue, human liver tissue.
Subcellular location: Apical cell membrane, Endosome lumen, Membrane, coated pit, Cell projection, dendrite, axon.
Recommended Dilutions:
  IHC-P
  IF-Tissue
  WB

1:1,000
1:50
1:2,000
Uniprot #: SwissProt: P98164 Human
Alternative names: Calcium sensor protein DBS Glycoprotein 330 gp330 Heymann nephritis antigen homolog Low-density lipoprotein receptor-related protein 2 LRP-2 Lrp2 LRP2_HUMAN Megalin
Images
HA721910_1.jpg Fig1: Western blot analysis of Lrp2 / Megalin on human kidney tissue lysates with Rabbit anti-Lrp2 / Megalin antibody (HA721910) at 1/2,000 dilution.

Lysates/proteins at 40 µg/Lane.

Predicted band size: 522 kDa
Observed band size: 600 kDa

Exposure time: 2 minutes;

4-20% 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 (HA721910) at 1/2,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.
HA721910_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human kidney tissue with Rabbit anti-Lrp2 / Megalin antibody (HA721910) at 1/1000 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 (HA721910) at 1/200 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.
HA721910_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded human skeletal muscle tissue (negative) with Rabbit anti-Lrp2 / Megalin antibody (HA721910) at 1/1000 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 (HA721910) at 1/200 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.
HA721910_4.jpg Fig4: Immunofluorescence analysis of paraffin-embedded human liver tissue labeling Lrp2 / Megalin with Rabbit anti-Lrp2 / Megalin antibody (HA721910) at 1/50 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 10% negative goat serum for 1 hour at room temperature, washed with PBS, and then probed with the primary antibody (HA721910, green) at 1/50 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue).
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.