Prolactin Receptor Mouse Monoclonal Antibody [A6E4]
cat.: HA600099
Product Type: Mouse monoclonal IgG1, primary antibodies
Species reactivity: Human
Applications: WB, IF-Cell, IHC-P, FC
Clonality: Monoclonal
Clone number: A6E4
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: PBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 2ug/ul
Purification: Protein A affinity purified.
Molecular weight: Predicted band size: 70 kDa
Isotype: IgG1
Immunogen: Recombinant protein within Human Prolactin Receptor aa 150-350 / 622.
Positive control: 293T cell lysate, Hela cell lysate, MCF-7, human kidney tissue, human pancreas tissue, HeLa.
Subcellular location: Membrane, Secreted.
Recommended Dilutions:
  WB
  IF-Cell
  IHC-P
  FC

1:500
1:100
1:200
1:1,000
Uniprot #: SwissProt: P16471 Human
Alternative names: AI987712 CLONE SPM213 CPRLP Delta 4-delta 7/11 truncated prolactin receptor Delta 4-SF1b truncated prolactin receptor HPRL hPRL receptor hPRLrI Lactogen receptor MFAB MGC105486 OPR OTTHUMP00000115998 Pr-1 Pr-3 PRL R PRL-R PRLR Prlr-rs1 PRLR_HUMAN Prolactin receptor a Prolactin receptor Prolactin receptor delta 7/11 RATPRLR Secreted prolactin binding protein Truncated testis-specific box 1-C prolactin receptor wu:fj65c07
Images
HA600099_1.jpg Fig1: Western blot analysis of Prolactin Receptor on different lysates with Mouse anti-Prolactin Receptor antibody (HA600099) at 1/500 dilution.

Lane 1: 293T cell lysate (10 µg/Lane)
Lane 2: Hela cell lysate (10 µg/Lane)

Predicted band size: 70 kDa
Observed band size: 100 kDa

Exposure time: 2 minutes;

8% 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 (HA600099) at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody (HA1006) at 1/100,000 dilution was used for 1 hour at room temperature.
HA600099_2.jpg Fig2: Immunocytochemistry analysis of MCF-7 cells labeling Prolactin Receptor with Mouse anti-Prolactin Receptor antibody (HA600099) at 1/100 dilution.

Cells were fixed in 4% paraformaldehyde for 30 minutes, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes, and then blocked with 2% BSA for 30 minutes at room temperature. Cells were then incubated with Mouse anti-Prolactin Receptor antibody (HA600099) at 1/100 dilution in 2% BSA overnight at 4 ℃. Goat Anti-Mouse IgG H&L (iFluor™ 488, HA1125) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.
HA600099_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded human kidney tissue with Mouse anti-Prolactin Receptor antibody (HA600099) 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 (HA600099) 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.
HA600099_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded human pancreas tissue with Mouse anti-Prolactin Receptor antibody (HA600099) 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 (HA600099) 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.
HA600099_5.jpg Fig5: Flow cytometric analysis of HeLa cells labeling Prolactin Receptor.

Cells were fixed and permeabilized. Then stained with the primary antibody (HA600099, 1/1,000) (red) compared with Mouse IgG1 Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Mouse IgG Secondary antibody (HA1125) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Note: All products are “FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE”.