OLIG2抗体 [HL6811]

OLIG2 antibody [HL6811] detects OLIG2 protein by immunohistochemical analysis.
Sample: Paraffin-embedded rat cerebral cortex.
OLIG2 stained by OLIG2 antibody [HL6811] (GTX649625) diluted at 1:200.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min

OLIG2 antibody [HL6811] detects OLIG2 protein by immunohistochemical analysis.
Sample: Paraffin-embedded rat hippocampus.
OLIG2 stained by OLIG2 antibody [HL6811] (GTX649625) diluted at 1:200.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min

OLIG2 antibody [HL6811] detects OLIG2 protein by immunohistochemical analysis.
Sample: Paraffin-embedded mouse tissues.
OLIG2 stained by OLIG2 antibody [HL6811] (GTX649625) diluted at 1:200.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min

OLIG2 antibody [HL6811] detects OLIG2 protein by immunohistochemical analysis.
Sample: Paraffin-embedded mouse tissues.
OLIG2 stained by OLIG2 antibody [HL6811] (GTX649625) diluted at 1:200.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min

Human tissue extract (5 μg) was separated by 12% SDS-PAGE, and the membrane was blotted with OLIG2 antibody [HL6811] (GTX649625) diluted at 1:500. 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 12% SDS-PAGE, and the membrane was blotted with OLIG2 antibody [HL6811] (GTX649625) 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 12% SDS-PAGE, and the membrane was blotted with OLIG2 antibody [HL6811] (GTX649625) 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.