Product Type: | Rabbit polyclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse |
Applications: | WB, IF-Cell, IHC-P, FC |
Clonality: | Polyclonal |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | 1*TBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Immunogen affinity purified. |
Molecular weight: | Predicted band size: 96 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein within human VLDL Receptor aa 400-630. |
Positive control: | MCF7 cell lysates, mouse brain tissue, human skeletal muscle tissue. |
Subcellular location: | Cell membrane, Membrane, clathrin-coated pit. |
Recommended Dilutions:
WB IHC-P |
1:1,000 1:50-1:200 |
Uniprot #: | SwissProt: P98155 Human | P98156 Mouse |
Alternative names: | FLJ35024 Very low density lipoprotein receptor Very low-density lipoprotein receptor VLDL R VLDL receptor VLDL-R VLDLR VLDLR_HUMAN VLDLRCH |
Fig1:
Western blot analysis of VLDL Receptor on MCF7 cell lysates with Rabbit anti-VLDL Receptor antibody (HA500194) at 1/1,000 dilution. Lysates/proteins at 30 µg/Lane. Predicted band size: 96 kDa Observed band size: 130 kDa Exposure time: 43 seconds; 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 (HA500194) at 1/1,000 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. |
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Fig2: Immunohistochemical analysis of paraffin-embedded mouse brain tissue using anti-VLDL Receptor antibody. 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 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA500194, 1/100) for 30 minutes 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. | |
Fig3: Immunohistochemical analysis of paraffin-embedded human skeletal muscle tissue using anti-VLDL Receptor antibody. 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 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA500194, 1/100) for 30 minutes 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. |