PRDX3 Monoclonal Antibody, IgG2b, Clone: [12A10C12], Unconjugated, Mouse

Catalog Number: CSB-MA018656A0M
Article Name: PRDX3 Monoclonal Antibody, IgG2b, Clone: [12A10C12], Unconjugated, Mouse
Biozol Catalog Number: CSB-MA018656A0M
Supplier Catalog Number: CSB-MA018656A0m
Alternative Catalog Number: CSB-MA018656A0M-100UL, CSB-MA018656A0M-50UL
Manufacturer: Cusabio
Host: Mouse
Category: Antikörper
Application: ELISA, FC, IF, IHC, WB
Species Reactivity: Human
Conjugation: Unconjugated
Alternative Names: Antioxidant protein 1 antibody, AOP 1 antibody, AOP-1 antibody, AOP1 antibody, HBC189 antibody, MER5 antibody, MGC104387 antibody, MGC24293 antibody, mitochondrial antibody, peroxiredoxin 3 antibody, Peroxiredoxin III antibody, Peroxiredoxin-3 antibody, PRDX3 antibody, PRDX3_HUMAN antibody, PRO1748 antibody, Protein MER5 homolog antibody, PRX III antibody, Prx-III antibody, PRX3 antibody, SP 22 antibody, SP-22 antibody, SP22 antibody, Thioredoxin dependent peroxide reductase mitochondrial antibody, Thioredoxin-dependent peroxide reductase antibody
Clonality: Monoclonal
Clone Designation: [12A10C12]
Isotype: IgG2b
UniProt: P30048
Buffer: Preservative: 0.03% Proclin 300<br />Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
Purity: >95%, Protein G purified
Form: Liquid
Target: PRDX3
Application Dilute: Recommended dilution: WB:1:1000-1:5000, IHC:1:50-1:200, IF:1:50-1:200, FC:1:50-1:200
Overlay Peak curve showing Hela cells stained with CSB-MA018656A0m (red line) at 1:50. The cells were incubated in 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1µg/1*106cells) for 1h at 4C. The secondary antibody used was FITC-conjugated Goat Anti-Mouse IgG(H+L) at 1/100 dilution for 30min at 4C. Isotype control antibody (green line) was mouse IgG1 (1µg/1*106cells) used under the same conditions. Acquisition of >10,000 events was performed.
Immunofluorescence staining of Hela cells with(CSB-MA018656A0m)at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated AffiniPure Goat Anti-Mouse IgG (H+L).
Immunofluorescence staining of MCF7 cells with(CSB-MA018656A0m)at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated AffiniPure Goat Anti-Mouse IgG (H+L).
IHC image of CSB-MA018656A0m diluted at 1:50 and staining in paraffin-embedded human prostate tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
IHC image of CSB-MA018656A0m diluted at 1:50 and staining in paraffin-embedded human endometrial cance tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
Western Blot
Positive WB detected in: Hela whole cell lysate, MCF7 whole cell lysate, 293T whole cell lysate, JK whole cell lysate, HepG2 whole cell lysate, Raji whole cell lysate, U87 whole cell lysate
All lanes: PRDX3 antibody at 1:1000
Secondary
Goat polyclonal to mouse IgG at 1/50000 dilution
Predicted band size: 28 kDa
Observed band size: 28 KDa
Exposure time:5min