CD63抗体 [HL4361]

Whole cell extract (30 μg) was separated by 12% SDS-PAGE, and the membrane was blotted with CD63 antibody [HL4361] (GTX643611) 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.

CD63 antibody [HL4361] detects CD63 protein by immunohistochemical analysis.
Sample: Paraffin-embedded mouse tissues.
CD63 stained by CD63 antibody [HL4361] (GTX643611) diluted at 1:400.
Antigen Retrieval: Tris-EDTA buffer, pH 9.0, 15 min

CD63 antibody [HL4361] detects CD63 protein by immunohistochemical analysis.
Sample: Paraffin-embedded mouse tissues.
CD63 stained by CD63 antibody [HL4361] (GTX643611) diluted at 1:400.
Antigen Retrieval: Tris-EDTA buffer, pH 9.0, 15 min

CD63 antibody [HL4361] detects CD63 protein by immunohistochemical analysis.
Sample: Paraffin-embedded human placenta.
CD63 stained by CD63 antibody [HL4361] (GTX643611) diluted at 1:200.
Antigen Retrieval: Tris-EDTA buffer, pH 9.0, 15 min

CD63 antibody [HL4361] detects CD63 protein by immunohistochemical analysis.
Sample: Paraffin-embedded human tonsil.
CD63 stained by CD63 antibody [HL4361] (GTX643611) diluted at 1:2000.
Antigen Retrieval: Tris-EDTA buffer, pH 9.0, 15 min

Various whole cell extracts (30 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with CD63 antibody [HL4361] (GTX643611) diluted at 1:5000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.

Various whole cell extracts (30 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with CD63 antibody [HL4361] (GTX643611) 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.