NPY5R Recombinant Rabbit Monoclonal Antibody [JE61-56]
cat.: HA720061
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IF-Cell, IHC-P, FC
Clonality: Monoclonal
Clone number: JE61-56
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: 51 kDa
Isotype: IgG
Immunogen: Synthetic peptide within human NPY5R aa 1-50/445.
Positive control: Human brain tissue lysate, rat brain tissue lysate, A549 cell lysate, mouse spleen tissue lysate, A549, SiHa, human skin tissue, mouse brain tissue.
Subcellular location: Cell membrane.
Recommended Dilutions:
  WB
  IF-Cell
  IHC-P
  FC

1:500-1:2,000
1:50-1:200
1:50-1:200
1:500-1:1,000
Uniprot #: SwissProt: Q15761 Human | O70342 Mouse | Q63634 Rat
Alternative names: Neuropeptide Y receptor type 5 Neuropeptide Y receptor Y5 NPY 5R NPY R5 NPY Y5 NPY Y5 receptor NPY-Y5 receptor NPY5 R NPY5-R NPY5R NPY5R_HUMAN NPYR 5 NPYR5 NPYY 5 NPYY5 NPYY5-R Y5 receptor
Images
HA720061_1.jpg Fig1: Western blot analysis of NPY5R on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA720061, 1/500) was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:200,000 dilution was used for 1 hour at room temperature.
Positive control:
Lane 1: Human brain tissue lysate
Lane 2: Rat brain tissue lysate
Lane 3: A549 cell lysate
Lane 4: Mouse spleen tissue lysate
HA720061_2.jpg Fig2: ICC staining of NPY5R in A549 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 10% negative goat serum for 15 minutes at room temperature. Cells were probed with the primary antibody (HA720061, 1/200) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).
HA720061_3.jpg Fig3: ICC staining of NPY5R in SiHa cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 10% negative goat serum for 15 minutes at room temperature. Cells were probed with the primary antibody (HA720061, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue).
HA720061_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded human skin tissue using anti-NPY5R antibody. 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 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA720061, 1/50) for 30 minutes 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.
HA720061_5.jpg Fig5: Immunohistochemical analysis of paraffin-embedded mouse brain tissue using anti-NPY5R antibody. 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 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA720061, 1/50) for 30 minutes 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.
HA720061_6.jpg Fig6: Flow cytometric analysis of NPY5R was done on A549 cells. The cells were stained with the primary antibody (HA720061, 1ug/ml) (red) compared with Rabbit IgG, monoclonal - Isotype Control (green). After incubation of the primary antibody at at +4℃ for 1 hour, the cells were stained with a Alexa Fluor®488 conjugate-Goat anti-Rabbit IgG Secondary antibody at 1/1,000 dilution for 30 min at +4℃ (dark incubation).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”.