ALDH1L1 Recombinant Rabbit Monoclonal Antibody [JU53-54]
cat.: ET7106-64
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IHC-P, IF-Tissue, IHC-Fr
Clonality: Monoclonal
Clone number: JU53-54
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. 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: 99 kDa
Isotype: IgG
Immunogen: Recombinant protein within Human ALDH1L1 aa 155-375 .
Positive control: A431, A549, LOVO, human liver tissue, human kidney tissue, mouse liver tissue, rat kidney tissue, rat brain tissue, mouse brain tissue.
Subcellular location: Cytoplasm.
Recommended Dilutions:
  WB
  IHC-P
  IF-Tissue
  IHC-Fr

1:500-2,000
1:200-1:1,000
1:50-1:200
1:500
Uniprot #: SwissProt: O75891 Human | Q8R0Y6 Mouse | P28037 Rat
Alternative names: 10 formyltetrahydrofolate dehydrogenase 10 FTHFDH 10-formyltetrahydrofolate dehydrogenase 10-FTHFDH AL1L1_HUMAN Aldehyde dehydrogenase 1 family member L1 Aldehyde dehydrogenase family 1 member L1 aldh1l1 Cytosolic 10-formyltetrahydrofolate dehydrogenase DKFZp781N0997 EC 1.5.1.6 FDH formyltetrahydrofolate dehydrogenase FTHFD OTTHUMP00000155221 OTTHUMP00000214696 OTTHUMP00000214700 OTTHUMP00000222724
Images
ET7106-64_1.jpg Fig1: Immunofluorescence analysis of frozen mouse brain tissue with Rabbit anti-ALDH1L1 antibody (ET7106-64) 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 (ET7106-64, green) at 1/500 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).
ET7106-64_2.jpg Fig2: Immunofluorescence analysis of frozen rat brain tissue with Rabbit anti-ALDH1L1 antibody (ET7106-64) 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 (ET7106-64, green) at 1/500 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).
ET7106-64_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded mouse brain tissue with Rabbit anti-ALDH1L1 antibody (ET7106-64) at 1/1,000 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 (ET7106-64) at 1/1,000 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.
ET7106-64_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded rat brain tissue with Rabbit anti-ALDH1L1 antibody (ET7106-64) at 1/200 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 (ET7106-64) 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.
ET7106-64_5.jpg Fig5: Immunofluorescence analysis of paraffin-embedded rat brain tissue labeling ALDH1L1 with Rabbit anti-ALDH1L1 antibody (ET7106-64) 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 (ET7106-64, 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).
ET7106-64_6.jpg Fig6: Immunofluorescence analysis of paraffin-embedded mouse brain tissue labeling ALDH1L1 with Rabbit anti-ALDH1L1 antibody (ET7106-64) at 1/200 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 (ET7106-64, green) at 1/200 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).
ET7106-64_7.jpg Fig7: Immunohistochemical analysis of paraffin-embedded human liver tissue using anti-ALDH1L1 antibody. Counter stained with hematoxylin.
ET7106-64_8.jpg Fig8: Immunohistochemical analysis of paraffin-embedded human kidney tissue using anti-ALDH1L1 antibody. Counter stained with hematoxylin.
ET7106-64_9.jpg Fig9: Immunohistochemical analysis of paraffin-embedded mouse liver tissue using anti-ALDH1L1 antibody. Counter stained with hematoxylin.
ET7106-64_10.jpg Fig10: Immunohistochemical analysis of paraffin-embedded rat kidney tissue using anti-ALDH1L1 antibody. Counter stained with hematoxylin.
ET7106-64_11.jpg Fig11: Western blot analysis of ALDH1L1 on mouse liver tissue lysates using anti-ALDH1L1 antibody at 1/500 dilution.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.