Wild-type (WT) and PRDX1 knockout (KO) U2OS cell extracts (10 μg) were separated by gradient gel% SDS-PAGE, and the membrane was blotted with PRX I antibody [N1C3] (GTX113793) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.
Data provided by YCharOS Inc., an open science company with the mission of characterizing commercially available antibody reagents for all human proteins using knockout technology.

Wild-type (WT) and PRDX1 knockout (KO) U2OS cell extracts (10 μg) were separated by gradient gel% SDS-PAGE, and the membrane was blotted with PRX I antibody [N1C3] (GTX113793) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.<br><I>Data provided by YCharOS Inc., an open science company with the mission of characterizing commercially available antibody reagents for all human proteins using knockout technology.</I>

Various whole cell extracts (30 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with PRX I antibody [N1C3] (GTX113793) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Sample (30 ug of whole cell lysate)
A: U87-MG
B: MCF-7
12% SDS PAGE
GTX113793 diluted at 1:1000

Immunohistochemical analysis of paraffin-embedded HT29 xenograft, using PRX I(GTX113793) antibody at 1:100 dilution.
Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min

Sample (50 ug of whole cell lysate)
A: mouse brain
12% SDS PAGE
GTX113793 diluted at 1:1000