WB
Western blot analysis of ALDH1L1 on different lysates with Rabbit anti-ALDH1L1 antibody at 1/5,000 dilution.
Lane 1: Mouse brain tissue lysate,
Lane 2: Mouse liver tissue lysate,
Lane 3: Mouse kidney tissue lysate,
Lane 4: Rat brain tissue lysate,
Lane 5: Rat liver tissue lysate,
Lane 6: Rat kidney tissue lysate,
Lysates/proteins at 40 µg/Lane.
Exposure time: 10 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 at 1/5,000 dilution was used in primary antibody dilution at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1/50,000 dilution was used for 1 hour at room temperature.
IHC
Immunohistochemical analysis of paraffin-embedded human liver tissue with Rabbit anti-ALDH1L1 antibody 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 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.
IHC
Immunohistochemical analysis of paraffin-embedded mouse liver tissue with Rabbit anti-ALDH1L1 antibody 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 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.
IHC
Immunohistochemical analysis of paraffin-embedded rat liver tissue with Rabbit anti-ALDH1L1 antibody 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 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.
IF-F
Species: Mouse,
Site: Cerebral cortex,
Sample: Frozen section,
Antibody concentration: 1:500,
Antigen retrieval: Not required.
IF-F
Species: Rat,
Site: Cerebral cortex,
Sample: Frozen section,
Antibody concentration: 1:500,
Antigen retrieval: Not required.
IF-P
Species: Mouse,
Site: Cerebral cortex,
Sample: Paraffin-embedded section,
Antibody concentration: 1:500.
IF-P
Species: Rat,
Site: Cerebral cortex,
Sample: Paraffin-embedded section,
Antibody concentration: 1:500.