Optimal dilutions for each application to be determined by the researcher.
Application Notes:
WB: 1:1000 - 1:4000IF: 1:50 - 1:200
Western blot analysis of extracts of various cell lines, using ZP2 antibody (13-444) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 10s.
Immunofluorescence analysis of rat oophoroma cells using ZP2 antibody (13-444) at dilution of 1:100. Blue: DAPI for nuclear staining.
Immunofluorescence analysis of rat oophoroma cells using ZP2 antibody (13-444) at dilution of 1:100. Blue: DAPI for nuclear staining.
Immunofluorescence analysis of mouse oophoroma cells using ZP2 antibody (13-444) at dilution of 1:100. Blue: DAPI for nuclear staining.
Immunofluorescence analysis of mouse oophoroma cells using ZP2 antibody (13-444) at dilution of 1:100. Blue: DAPI for nuclear staining.
Immunofluorescence analysis of mouse oophoroma cells using ZP2 antibody (13-444) at dilution of 1:100. Blue: DAPI for nuclear staining.
Immunofluorescence analysis of mouse oophoroma cells using ZP2 antibody (13-444) at dilution of 1:100. Blue: DAPI for nuclear staining.
Immunofluorescence analysis of mouse oophoroma cells using ZP2 antibody (13-444) at dilution of 1:100. Blue: DAPI for nuclear staining.
Immunofluorescence analysis of mouse oophoroma cells using ZP2 antibody (13-444) at dilution of 1:100. Blue: DAPI for nuclear staining.
* VAT and and shipping costs not included. Errors and price changes excepted