Western blotting analysis using anti-SNRPC antibody (Cat#65623). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-SNRPC antibody (Cat#65623, 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).
Western blotting analysis using anti-SNRPC antibody (Cat#65623). SNRPC expression in wild-type (WT) and SNRPC shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with anti-SNRPC antibody (Cat#65623, 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 SNRPC expression in HAP-1 cells using anti-SNRPC antibody (Cat#65623, 1:2,000). Green, isotype control; red, SNRPC.
SNRPC; Small Nuclear Ribonucleoprotein Polypeptide C; U1-C; Yhc1; U1 Small Nuclear Ribonucleoprotein C; U1 SnRNP C; U1C; U1 Small Nuclear RNP Specific C; U1 SnRNP Protein C
Applications Tested: Western blotting (WB), flow cytometry (FCM)
Immunogen
A synthesized peptide derived from human SNRPC
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
Western blotting analysis using anti-SNRPC antibody (Cat#65623). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-SNRPC antibody (Cat#65623, 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).
Western blotting analysis using anti-SNRPC antibody (Cat#65623). SNRPC expression in wild-type (WT) and SNRPC shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with anti-SNRPC antibody (Cat#65623, 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 SNRPC expression in HAP-1 cells using anti-SNRPC antibody (Cat#65623, 1:2,000). Green, isotype control; red, SNRPC.
Western blotting analysis using anti-SNRPC antibody (Cat#65623). Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-SNRPC antibody (Cat#65623, 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).
Western blotting analysis using anti-SNRPC antibody (Cat#65623). SNRPC expression in wild-type (WT) and SNRPC shRNA knockdown (KD) HeLa cells with 30 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with anti-SNRPC antibody (Cat#65623, 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 SNRPC expression in HAP-1 cells using anti-SNRPC antibody (Cat#65623, 1:2,000). Green, isotype control; red, SNRPC.
