WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
GTX109001 WB Image
Immunohistochemical analysis of paraffin-embedded N87 xenograft, using SLC25A13(GTX109001) antibody at 1:500 dilution. Antigen Retrieval: Trilogy™ (EDTA based, pH 8.0) buffer, 15min
SLC25A13 antibody [N3C2], Internal detects SLC25A13 protein at cytoplasm in mouse kidney by immunohistochemical analysis. Sample: Paraffin-embedded mouse kidney. SLC25A13 antibody [N3C2], Internal (GTX109001) diluted at 1:500.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min
Rat tissue extract (50 μg) was separated by 7.5% SDS-PAGE, and the membrane was blotted with SLC25A13 antibody [N3C2], Internal (GTX109001) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.
Sample (50 μg of whole cell lysate) A: mouse liver 7.5% SDS PAGE GTX109001 diluted at 1:1000 The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.
Whole cell extract (30 μg) was separated by 7.5% SDS-PAGE, and the membranes were blotted with SLC25A13 antibody [N3C2], Internal (GTX109001) diluted at 1:1000 and competitor's antibody (10789-1-AP) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.
*The competitor is not affiliated with GeneTex and does not endorse this product.
SLC25A13 antibody [N3C2], Internal detects SLC25A13 protein at mitochondria by immunofluorescent analysis. Sample: HeLa cells were fixed in 4% paraformaldehyde at RT for 15 min. Green: SLC25A13 protein stained by SLC25A13 antibody [N3C2], Internal (GTX109001) diluted at 1:500. Blue: Hoechst 33342 staining.
SLC25A13 antibody [N3C2], Internal detects SLC25A13 protein at cytoplasm in mouse kidney by immunohistochemical analysis. Sample: Paraffin-embedded mouse kidney. SLC25A13 antibody [N3C2], Internal (GTX109001) diluted at 1:500.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min
Wild-type (WT) and SLC25A13 knockout (KO) HeLa cell extracts (30 μg) were separated by 7.5% SDS-PAGE, and the membrane was blotted with SLC25A13 antibody [N3C2], Internal (GTX109001) diluted at 1:3000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.
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