Anti-P2X7/P2RX7 Antibody Picoband, Rabbit, Polyclonal

Artikelnummer: BOB-A01208-3
Artikelname: Anti-P2X7/P2RX7 Antibody Picoband, Rabbit, Polyclonal
Artikelnummer: BOB-A01208-3
Hersteller Artikelnummer: A01208-3
Alternativnummer: BOB-A01208-3-100UG
Hersteller: Boster Bio
Wirt: Rabbit
Kategorie: Antikörper
Applikation: ELISA, FC, IHC, WB
Spezies Reaktivität: Human, Mouse, Rat
Immunogen: E.coli-derived human P2X7/P2RX7 recombinant protein (Position: S47-K311).
Alternative Synonym: P2RX7, P2X7
Boster Bio Anti-P2X7/P2RX7 Antibody Picoband catalog A01208-3. Tested in ELISA, Flow Cytometry, IHC, WB applications. This antibody reacts with Human, Mouse, Rat. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.
Klonalität: Polyclonal
Konzentration: Adding 0.2 ml of distilled water will yield a concentration of 500 µg/ml.
Molekulargewicht: Observed Molecular Weight: 70 kDa. Calculated Molecular Weight: 123799 MW
NCBI: 5027
UniProt: Q99572
Puffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.
Reinheit: Immunogen affinity purified.
Formulierung: Lyophilized
Target-Kategorie: P2X purinoceptor 7
Application Verdünnung: Western blot, 0.25-0.5 µg/ml, Mouse, Rat Immunohistochemistry(Paraffin-embedded Section), 2-5 µg/ml, Human, Rat Flow Cytometry (Fixed), 1-3 µg/1x106 cells, Human ELISA, 0.1-0.5 µg/ml, -
IHC analysis of P2X7/P2RX7 using anti-P2X7/P2RX7 antibody (A01208-3). P2X7/P2RX7 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 µg/ml rabbit anti-P2X7/P2RX7 Antibody (A01208-3) overnight at 4C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog SA1022) with DAB as the chromogen.
IHC analysis of P2X7/P2RX7 using anti-P2X7/P2RX7 antibody (A01208-3). P2X7/P2RX7 was detected in a paraffin-embedded section of human gall bladder adenosquamous carcinomar tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 µg/ml rabbit anti-P2X7/P2RX7 Antibody (A01208-3) overnight at 4C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog SA1022) with DAB as the chromogen.
IHC analysis of P2X7/P2RX7 using anti-P2X7/P2RX7 antibody (A01208-3). P2X7/P2RX7 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 µg/ml rabbit anti-P2X7/P2RX7 Antibody (A01208-3) overnight at 4C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog SA1022) with DAB as the chromogen.
IHC analysis of P2RX7 using anti-P2RX7 antibody (A01208-3). P2RX7 was detected in a paraffin-embedded section of human cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (p
Western blot analysis of P2X7/P2RX7 using anti-P2X7/P2RX7 antibody (A01208-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P2X7/P2RX7 antigen affinity purified polyclonal antibody (Catalog A01208-3) at 0.5 µg/mL overnight at 4C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog EK1002) with Tanon 5200 system. A specific band was detected for P2X7/P2RX7 at approximately 70 kDa. The expected band size for P2X7/P2RX7 is at 70 kDa.
Flow Cytometry analysis of THP-1 cells using anti-P2X7/P2RX7 antibody (A01208-3). Overlay histogram showing THP-1 cells stained with A01208-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-P2X7/P2RX7 Antibody (A01208-3, 1 µg/1x106 cells) for 30 min at 20C. DyLight488 conjugated goat anti-rabbit IgG (BA1127, 5-10 µg/1x106 cells) was used as secondary antibody for 30 minutes at 20C. Isotype control antibody (Green line) was rabbit IgG (1 µg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.