StAR Recombinant Rabbit Monoclonal Antibody [JE32-23]
cat.: HA721469
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human
Applications: WB, IHC-P
Clonality: Monoclonal
Clone number: JE32-23
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: 32 kDa
Isotype: IgG
Immunogen: Synthetic peptide within Human StAR aa 235-285.
Positive control: K-562 cell lysates, human adrenal gland tissue.
Subcellular location: Mitochondrion.
Recommended Dilutions:
  WB
  IHC-P

1:1,000
1:1,000
Uniprot #: SwissProt: P49675 Human
Alternative names: Cholesterol trafficker Luteinizing hormone induced protein mitochondrial Mitochondrial steroid acute regulatory protein StAR StAR related lipid transfer (START) domain containing 1 STAR_HUMAN StARD1 START domain containing 1 START domain containing protein 1 START domain-containing protein 1 Steroid acute regulatory protein Steroidogenic acute regulator Steroidogenic acute regulatory protein Steroidogenic acute regulatory protein mitochondrial
Images
HA721469_1.jpg Fig1: Western blot analysis of StAR on K-562 cell lysates with Rabbit anti-StAR antibody (HA721469) at 1/1,000 dilution.

Lysates/proteins at 20 µg/Lane.

Predicted band size: 32 kDa
Observed band size: 26 kDa

Exposure time: 3 minutes;

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 (HA721469) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:100,000 dilution was used for 1 hour at room temperature.
HA721469_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human adrenal gland tissue with Rabbit anti-StAR antibody (HA721469) 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 (HA721469) 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”.