Apolipoprotein E Recombinant Antibody [PSH10-52] - Rat IgG1 (Chimeric)
cat.: HA601391
Product Type: Recombinant Chimeric Antibody IgG1, primary antibodies
Species reactivity: Mouse, Rat
Applications: IHC-Fr, IHC-P, WB
Clone number: PSH10-52
Form: Liquid
Storage condition: Shipped at 4℃. Store at +4℃ short term (1-2 weeks). It is recommended to aliquot into single-use upon delivery. Store at -20℃ long term.
Storage buffer: 1*PBS (pH7.4), 0.1% BSA, 40% Glycerol, 0.2% Proclean 950.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 36 kDa
Isotype: IgG1
Immunogen: Recombinant protein within Mouse Apolipoprotein E aa 19-311.
Positive control: Mouse brain tissue, rat brain tissue, rat striatum tissue, Mouse brain tissue lysate, Mouse liver tissue lysate, Rat brain tissue lysate, Rat liver tissue lysate.
Subcellular location: Secreted, extracellular space, extracellular matrix.
Recommended Dilutions:
  IHC-Fr
  IHC-P
  WB

1:500
1:2,000
1:5,000
Uniprot #: SwissProt: P08226 Mouse | P02650 Rat
Alternative names: AD2 Apo-E APOE APOE_HUMAN APOEA Apolipoprotein E Apolipoprotein E3 ApolipoproteinE Apoprotein LDLCQ5 LPG
Images
HA601391_1.jpg Fig1: Immunofluorescence analysis of frozen mouse brain tissue with Rat anti-Apolipoprotein E antibody (HA601391) at 1/500 dilution.

The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for about 2 minutes in microwave oven. 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 (HA601391, green) at 1/500 dilution overnight at 4 ℃, washed with PBS. Goat Anti-Rat IgG H&L (iFluor™ 488, HA1133) was used as the secondary antibody at 1/1,000 dilution. Nuclei were counterstained with DAPI (blue).
HA601391_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded mouse brain tissue with Rat anti-Apolipoprotein E antibody (HA601391) at 1/2,000 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 (HA601391) at 1/2,000 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.
HA601391_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded rat brain tissue with Rat anti-Apolipoprotein E antibody (HA601391) at 1/2,000 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 (HA601391) at 1/2,000 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.
HA601391_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded rat striatum tissue with Rat anti-Apolipoprotein E antibody (HA601391) at 1/2,000 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 (HA601391) at 1/2,000 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.
HA601391_5.jpg Fig5: Western blot analysis of Apolipoprotein E on different lysates with Rat anti-Apolipoprotein E antibody (HA601391) at 1/5,000 dilution.

Lane 1: Mouse brain tissue lysate
Lane 2: Mouse liver tissue lysate
Lane 3: C2C12 cell lysate (negative)
Lane 4: Rat brain tissue lysate
Lane 5: Rat liver tissue lysate

Lysates/proteins at 20 µg/Lane.

Predicted band size: 36 kDa
Observed band size: 33 kDa

Exposure time: 10 seconds; ECL: K1801;
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 (HA601391) at 1/5,000 dilution was used in primary antibody dilution (K1803) at 4℃ overnight. Goat Anti-Rat IgG H&L - HRP Secondary Antibody (HA1023) at 1/5,000 dilution was used for 1 hour at room temperature.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.