mouse monoclonal (AT2G2)
reactivity: human, mouse
application: western blot, ELISA, immunohistochemistry, enzyme immunoassay
reactivity: human, mouse
application: western blot, ELISA, immunohistochemistry, enzyme immunoassay
goat polyclonal
reactivity: human, mouse, rat, dog, cow
application: western blot, immunohistochemistry, enzyme immunoassay
reactivity: human, mouse, rat, dog, cow
application: western blot, immunohistochemistry, enzyme immunoassay
rabbit polyclonal
reactivity: human, mouse, rat
application: western blot, immunohistochemistry, immunoprecipitation
reactivity: human, mouse, rat
application: western blot, immunohistochemistry, immunoprecipitation
rabbit polyclonal
reactivity: human, mouse
application: western blot, ELISA, immunohistochemistry, immunocytochemistry, enzyme immunoassay
reactivity: human, mouse
application: western blot, ELISA, immunohistochemistry, immunocytochemistry, enzyme immunoassay
MBS9608333 staining HepG2 cells by IF/ICC. The samples were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25°C. Samples were then incubated with primary Ab(MBS9608333 1:200) and mouse anti-beta tubulin Ab(MBS9610328 1:200) for 1 hour at 37°C. An AlexaFluor594 conjugated goat anti-rabbit IgG(H+L) Ab(Red) and an AlexaFluor488 conjugated goat anti-mouse IgG(H+L) Ab(Green) were used as the secondary antibody.
MBS9608333 at 1/100 staining Human liver cancer tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22°C. An HRP conjugated goat anti-rabbit antibody was used as the secondary.
Western blot analysis of extracts from various samples, using ATGL Antibody. Lane 1: HepG2 cells, treated with blocking peptide;. Lane 2: HepG2 cells;. Lane 3: Hela cells.
quantity: 0.1 mL
price: 240 USD
to the supplier