NMU抗体 [HL5007]

Various whole cell extracts (30 μg) were separated by 15% SDS-PAGE, and the membrane was blotted with NMU antibody [HL5007] (GTX645100) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody. Corresponding RNA expression data are based on Human Protein Atlas program.

Various tissue extracts (50 μg) were separated by 15% SDS-PAGE, and the membrane was blotted with NMU antibody [HL5007] (GTX645100) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody, and the signal was developed with Trident femto Western HRP Substrate.

Various tissue extracts (50 μg) were separated by 15% SDS-PAGE, and the membrane was blotted with NMU antibody [HL5007] (GTX645100) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody, and the signal was developed with Trident femto Western HRP Substrate. Corresponding RNA expression data are based on NCBI database.

K562 whole cell extract and conditioned medium (30 μg) were separated by 15% SDS-PAGE, and the membrane was blotted with NMU antibody [HL5007] (GTX645100) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.