ADH4 Recombinant Rabbit Monoclonal Antibody [JE62-24]
cat.: HA722570
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human
Applications: WB, IHC-P
Clonality: Monoclonal
Clone number: JE62-24
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 40 kDa
Isotype: IgG
Immunogen: Recombinant protein within
Positive control: HeLa cell lysate, Human liver tissue lysate, human kidney tissue.
Subcellular location: Cytoplasm.
Recommended Dilutions:
  WB
  IHC-P

1:1,000
1:1,000
Uniprot #: SwissProt: P08319 Human
Alternative names: Ac1002 ADH 4 ADH-1 ADH-2 ADH2 Adh4 ADH4_HUMAN Alcohol dehydrogenase 4 (class II) pi polypeptide Alcohol dehydrogenase 4 Alcohol dehydrogenase class II pi chain Alcohol dehydrogenase pi isozyme ADH class II Aldehyde reductase Class II alcohol dehydrogenase 4 pi subunit
Images
HA722570_1.jpg Fig1: Western blot analysis of ADH4 on different lysates with Rabbit anti-ADH4 antibody (HA722570) at 1/1,000 dilution.

Lane 1: HeLa cell lysate (20 µg/Lane)
Lane 2: Human liver tissue lysate (40 µg/Lane)

Predicted band size: 40 kDa
Observed band size: 40 kDa

Exposure time: Lane 1: 1 minute; Lane 2: 3 minutes; 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 (HA722570) 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.
HA722570_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human kidney tissue with Rabbit anti-ADH4 antibody (HA722570) 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 (HA722570) 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.
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.