Flow cytometric analysis of EPH receptor B3 expression in C2C12 cells using EPH receptor B3 antibody (Cat#61361, 1:2,000). Green, isotype control; red, EPH receptor B3.
Western blotting analysis using anti-EPH receptor B3 antibody (Cat#61361). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-EPH receptor B3 antibody (Cat#61361, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Western blotting analysis using anti-EPH receptor B3 antibody (Cat#61361). EPH receptor B3 expression in wild-type (WT) and EPH receptor B3 (EPHB3) knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with anti-EPH receptor B3 antibody (Cat#61361, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Applications Tested: Western blotting (WB), flow cytometry (FCM)
Immunogen
A synthesized peptide derived from human Eph receptor B3
Isotype
Rabbit IgG
Storage Buffer
Supplied in PBS (pH 7.4) containing 50% glycerol, and 0.02% sodium azide.
Storage
Store at -20 °C for one year.
Recommended Dilutions
Western Blotting (WB): 1:1,000-1:5,000 Flow Cytometry (FCM): 1:2,000
Note
This product is for research use only.
Picture
Flow cytometric analysis of EPH receptor B3 expression in C2C12 cells using EPH receptor B3 antibody (Cat#61361, 1:2,000). Green, isotype control; red, EPH receptor B3.
Western blotting analysis using anti-EPH receptor B3 antibody (Cat#61361). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-EPH receptor B3 antibody (Cat#61361, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Western blotting analysis using anti-EPH receptor B3 antibody (Cat#61361). EPH receptor B3 expression in wild-type (WT) and EPH receptor B3 (EPHB3) knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with anti-EPH receptor B3 antibody (Cat#61361, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).
Flow cytometric analysis of EPH receptor B3 expression in C2C12 cells using EPH receptor B3 antibody (Cat#61361, 1:2,000). Green, isotype control; red, EPH receptor B3.
Western blotting analysis using anti-EPH receptor B3 antibody (Cat#61361). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-EPH receptor B3 antibody (Cat#61361, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using FeQ™ ECL Substrate Kit (Cat#226).
Western blotting analysis using anti-EPH receptor B3 antibody (Cat#61361). EPH receptor B3 expression in wild-type (WT) and EPH receptor B3 (EPHB3) knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with anti-EPH receptor B3 antibody (Cat#61361, 1:5,000) and HRP-conjugated goat anti-rabbit secondary antibody (Cat#201, 1:20,000) respectively. Image was developed using NaQ™ ECL Substrate Kit (Cat#716).