Figure 1. Western blot analysis of ABCE1 using anti-ABCE1 antibody (AZQ6TNW3). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: zebrafish embryo tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ABCE1 antigen affinity purified polyclonal antibody (AZQ6TNW3) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for ABCE1 at approximately 67 kDa. The expected band size for ABCE1 is at 67 kDa.

Figure 2. IHC analysis of ABCE1 using anti-ABCE1 antibody (AZQ6TNW3).
ABCE1 was detected in a paraffin-embedded section of zebrafish brain tissue. The tissue section was incubated with rabbit anti-ABCE1 Antibody (AZQ6TNW3) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1022) as the chromogen.

Figure 3. IHC analysis of ABCE1 using anti-ABCE1 antibody (AZQ6TNW3).
ABCE1 was detected in a paraffin-embedded section of zebrafish eye tissue. The tissue section was incubated with rabbit anti-ABCE1 Antibody (AZQ6TNW3) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1022) as the chromogen.

Figure 1. Western blot analysis of AFG3L2 using anti-AFG3L2 antibody (AZA9JRG9). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: zebrafish head tissue lysates,
Lane 2: zebrafish embryo tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-AFG3L2 antigen affinity purified polyclonal antibody (AZA9JRG9) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for AFG3L2 at approximately 80-90 kDa. The expected band size for AFG3L2 is at 89 kDa.

Figure 1. IHC analysis of AGO4 using anti-AGO4 antibody (AZK4IAH1).
AGO4 was detected in a paraffin-embedded section of zebrafish cerebellum tissue. The tissue section was incubated with rabbit anti-AGO4 Antibody (AZK4IAH1) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1022) as the chromogen.

Figure 1. IHC analysis of ATG5 using anti-ATG5 antibody (AZF1RDC0).
ATG5 was detected in a paraffin-embedded section of zebrafish cerebellum tissue. The tissue section was incubated with rabbit anti-ATG5 Antibody (AZF1RDC0) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1022) as the chromogen.

Figure 1. Western blot analysis of BAG5 using anti-BAG5 antibody (AZF1QGM6). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: zebrafish tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-BAG5 antigen affinity purified polyclonal antibody (AZF1QGM6) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for BAG5 at approximately 50 kDa. The expected band size for BAG5 is at 57 kDa.

Figure 2. IHC analysis of BAG5 using anti-BAG5 antibody (AZF1QGM6).
BAG5 was detected in a paraffin-embedded section of zebrafish heart tissue. The tissue section was incubated with rabbit anti-BAG5 Antibody (AZF1QGM6) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1022) as the chromogen.

Figure 1. Western blot analysis of C1QBP using anti-C1QBP antibody (AZF1R3F7). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: zebrafish tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-C1QBP antigen affinity purified polyclonal antibody (AZF1R3F7) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for C1QBP at approximately 35 kDa. The expected band size for C1QBP is at 30 kDa.

Figure 1. Western blot analysis of CCT2 using anti-CCT2 antibody (AZQ6PBW6). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: zebrafish tissue lysates,
Lane 2: zebrafish embryo tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-CCT2 antigen affinity purified polyclonal antibody (AZQ6PBW6) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for CCT2 at approximately 58 kDa. The expected band size for CCT2 is at 58 kDa.

Figure 1. Western blot analysis of CCT5 using anti-CCT5 antibody (AZQ6NVI6). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: zebrafish head tissue lysates,
Lane 2: zebrafish embryo tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-CCT5 antigen affinity purified polyclonal antibody (AZQ6NVI6) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for CCT5 at approximately 59 kDa. The expected band size for CCT5 is at 59 kDa.