P Glycoprotein Rabbit Polyclonal Antibody
cat.: HA500502
Product Type: Rabbit polyclonal IgG, primary antibodies
Species reactivity: Human, Mouse, Rat
Applications: WB, IHC-P, FC
Clonality: Polyclonal
Form: Liquid
Storage condition: Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage buffer: 1*TBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide.
Concentration: 1ug/ul
Purification: Immunogen affinity purified.
Molecular weight: Predicted band size: 141 kDa.
Isotype: IgG
Immunogen: Synthetic peptide within human P Glycoprotein aa 1,151-1,200.
Positive control: Mouse brain tissue lysate, rat brain tissue lysate, human brain tissue lysate, rat brain tissue, SH-SY5Y.
Subcellular location: Cell membrane, Apical cell membrane.
Recommended Dilutions:
  WB
  IHC-P
  FC

1:2,000-1:5,000
1:1,000
1:50-1:200
Uniprot #: SwissProt: P08183 Human | P06795 Mouse | P43245 Rat
Alternative names: ABC20 ABCB1 ATP binding cassette, sub family B (MDR/TAP), member 1 ATP-binding cassette sub-family B member 1 CD243 CLCS Colchicin sensitivity Doxorubicin resistance GP170 MDR1 MDR1_HUMAN Multidrug resistance 1 Multidrug resistance protein 1 P glycoprotein 1 P gp P-glycoprotein 1 PGY1
Images
HA500502_1.jpg Fig1: Western blot analysis of P Glycoprotein on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (HA500502, 1/2,000) was used in 5% BSA 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: Mouse brain tissue lysate
Lane 2: Rat brain tissue lysate
Lane 3: Human brain tissue lysate
HA500502_2.jpg Fig2: Immunohistochemical analysis of paraffin-embedded rat brain tissue using anti-P Glycoprotein 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 1% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA500502, 1/1,000) 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.
HA500502_3.jpg Fig3: Flow cytometric analysis of P Glycoprotein was done on SH-SY5Y cells. The cells were fixed, permeabilized and stained with the primary antibody (HA500502, 1ug/ml) (red) compared with Rabbit IgG, monoclonal - Isotype Control ( green). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor®488 conjugate-Goat anti-Rabbit IgG Secondary antibody at 1/1000 dilution for 30 minutes.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”.