PDGF B Recombinant Rabbit Monoclonal Antibody [JE75-16]
cat.: HA722003
Product Type: Recombinant Rabbit monoclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IHC-P
Clonality: Monoclonal
Clone number: JE75-16
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: 27 kDa
Isotype: IgG
Immunogen: Synthetic peptide within Human PDGF B aa 192-241 / 241.
Positive control: Human brain tissue lysate, mouse brain tissue lysate, rat brain tissue lysate, human kidney tissue, mouse brain tissue, rat brain tissue.
Subcellular location: Secreted.
Recommended Dilutions:
  WB
  IHC-P

1:2,000
1:2,000
Uniprot #: SwissProt: P01127 Human | P31240 Mouse | Q05028 Rat
Alternative names: Becaplermin c sis FLJ12858 Oncogene SIS PDGF 2 PDGF B chain PDGF Beta PDGF subunit B PDGF-2 PDGF2 Pdgfb PDGFB_HUMAN Platelet derived growth factor 2 Platelet derived growth factor B chain Platelet derived growth factor beta Platelet derived growth factor beta polypeptide (oncogene SIS) Platelet derived growth factor beta polypeptide (simian sarcoma viral (v sis) oncogene homolog) Platelet derived growth factor beta polypeptide Platelet-derived growth factor B chain Platelet-derived growth factor beta polypeptide Platelet-derived growth factor subunit B Proto-oncogene c-Sis Simian sarcoma viral (v sis) oncogene homolog SIS SSV v sis platelet derived growth factor beta polypeptide
Images
HA722003_1.jpg Fig1: Western blot analysis of PDGF B on different lysates with Rabbit anti-PDGF B antibody (HA722003) at 1/2,000 dilution.

Lane 1: Human brain tissue lysate
Lane 2: Mouse brain tissue lysate
Lane 3: Rat brain tissue lysate

Lysates/proteins at 40 µg/Lane.

Predicted band size: 27 kDa
Observed band size: 27 kDa

Exposure time: 2 minutes 18 seconds;

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 (HA722003) at 1/2,000 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.
HA722003_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded human kidney tissue with Rabbit anti-PDGF B antibody (HA722003) at 1/2,000 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 (HA722003) at 1/2,000 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.
HA722003_3.jpg Fig3: Immunohistochemical analysis of paraffin-embedded mouse brain tissue with Rabbit anti-PDGF B antibody (HA722003) at 1/2,000 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 (HA722003) at 1/2,000 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.
HA722003_4.jpg Fig4: Immunohistochemical analysis of paraffin-embedded rat brain tissue with Rabbit anti-PDGF B antibody (HA722003) at 1/2,000 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 (HA722003) at 1/2,000 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”.