Anti-LIF antibody was prepared from whole rabbit serum produced by repeated immunizations with a 16 amino acid synthetic peptide near the internal region of human LIF.
Anti-LIF Antibody has been tested for use in ELISA, Western Blotting and Immunofluorescence. Specific conditions for reactivity should be optimized by the end user. Expect a band at approximately 22 kDa in Western Blots of specific cell lysates and tissu
Immunofluorescence Validation of LIF. Cell: Mouse 3T3 Cells. Fixation: 4% paraformaldehyde-fixed. Primary Antibody: LIF at 20 µg/mL. Secondary: goat anti-rabbit IgG secondary antibody at 1:500 dilution (red).
Western Blot Validation of LIF. Load: 15 µg of mouse 3T3 lysates per lane. Primary Antibody: LIF at (lane A: 1 µg/mL, lane B: 2 µg/mL) for 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
Western Blot Validation of LIF. Load: 15 µg of human lysates per lane. Lane 1: Caco-2, Lane 2: Daudi, Lane 3: HeLa, Lane 4: HepG2, Lane 5: K562, Lane 6: MCF7, Lane 7: Jurkat, Lane 8: SK-N-SH. Primary Antibody: LIF at 1µg/mL at 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
Western Blot Validation of LIF. Load: 15 µg of recombinant protein per lane. Primary Antibody: LIF at (Lane 1: 1 µg/mL, lane 2: 2µg/mL, lane 3: 4 µg/mL) for 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
Western Blot Validation of LIF.Load: 15 µg of Mouse cell and tissue lysates per lane. Lane 1: 3T3/NIH, Lane 2: Mouse Colon, Lane 3: EL4. Primary Antibody: LIF, (1 µg/mL), 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
Western Blot Validation of LIF. Load: 15 µg of rat lung lysates per lane. Primary Antibody: LIF at (lane 1: 1 µg/mL, lane 2: 2 µg/mL) for 1h incubation at RT in 5% NFDM/TBST. Secondary: Goat anti-rabbit IgG HRP conjugate at 1:10000 dilution.
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