CD3 epsilon antibody [HL5848]

CD3 epsilon antibody [HL5848] detects CD3 epsilon protein by immunohistochemical analysis.
Sample: Paraffin-embedded rat tissues.
CD3 epsilon stained by CD3 epsilon antibody [HL5848] (GTX647166) diluted at 1:200.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min

CD3 epsilon antibody [HL5848] detects CD3 epsilon protein by immunohistochemical analysis.
Sample: Paraffin-embedded rat tissues.
CD3 epsilon stained by CD3 epsilon antibody [HL5848] (GTX647166) diluted at 1:200.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min

Various tissue extracts (50 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with CD3 epsilon antibody [HL5848] (GTX647166) 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.

CD3 epsilon antibody [HL5848] detects CD3 epsilon protein by immunohistochemical analysis.
Sample: Paraffin-embedded human tissues.
CD3 epsilon stained by CD3 epsilon antibody [HL5848] (GTX647166) diluted at 1:200.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min

CD3 epsilon antibody [HL5848] detects CD3 epsilon protein by immunofluorescent analysis.
Sample: Jurkat cells were fixed in 4% paraformaldehyde at RT for 15 min.
Green: CD3 epsilon stained by CD3 epsilon antibody [HL5848] (GTX647166) diluted at 1:500.
Blue: Fluoroshield™ with DAPI (GTX30920).

CD3 epsilon antibody [HL5848] detects CD3 epsilon protein by immunohistochemical analysis.
Sample: Paraffin-embedded mouse tissues.
CD3 epsilon stained by CD3 epsilon antibody [HL5848] (GTX647166) diluted at 1:200.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min

Various whole cell extracts (30 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with CD3 epsilon antibody [HL5848] (GTX647166) diluted at 1:410. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Various tissue extracts (50 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with CD3 epsilon antibody [HL5848] (GTX647166) 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 whole cell extracts (30 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with CD3 epsilon antibody [HL5848] (GTX647166) 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.