Figure 1. IHC analysis of Anp32e using anti-Anp32e antibody (DZ41646) .
Anp32e was detected in a paraffin-embedded section of zebrafish brain tissue. The tissue section was incubated with rabbit anti-Anp32e Antibody (DZ41646) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

Figure 2. IHC analysis of Anp32e using anti-Anp32e antibody (DZ41646) .
Anp32e was detected in a paraffin-embedded section of zebrafish heart tissue. The tissue section was incubated with rabbit anti-Anp32e Antibody (DZ41646) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

Figure 3. IHC analysis of Anp32e using anti-Anp32e antibody (DZ41646) .
Anp32e was detected in a paraffin-embedded section of zebrafish intestines tissue. The tissue section was incubated with rabbit anti-Anp32e Antibody (DZ41646) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

Figure 1. IHC analysis of aqp8a.1 using anti-aqp8a.1 antibody (DZ41642) .
aqp8a.1 was detected in a paraffin-embedded section of zebrafish heart tissue. The tissue section was incubated with rabbit anti-aqp8a.1 Antibody (DZ41642) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

Figure 1. IHC analysis of gpr179 using anti-gpr179 antibody (DZ41643) .
gpr179 was detected in a paraffin-embedded section of zebrafish brain tissue. The tissue section was incubated with rabbit anti-gpr179 Antibody (DZ41643) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

Figure 2. IHC analysis of gpr179 using anti-gpr179 antibody (DZ41643) .
gpr179 was detected in a paraffin-embedded section of zebrafish brain tissue. The tissue section was incubated with rabbit anti-gpr179 Antibody (DZ41643) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

Figure 1. IHC analysis of ABCB11 using anti-ABCB11 antibody (DZ01657) .
ABCB11 was detected in a paraffin-embedded section of zebrafish liver tissue. The tissue section was incubated with rabbit anti-ABCB11 Antibody (DZ01657) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

Figure 1. IHC analysis of ABCC12 using anti-ABCC12 antibody (DZ10852) .
ABCC12 was detected in a paraffin-embedded section of zebrafish colon tissue. The tissue section was incubated with rabbit anti-ABCC12 Antibody (DZ10852) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

Figure 2. IHC analysis of ABCC12 using anti-ABCC12 antibody (DZ10852) .
ABCC12 was detected in a paraffin-embedded section of zebrafish liver tissue. The tissue section was incubated with rabbit anti-ABCC12 Antibody (DZ10852) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

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 # AR1027) 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 # AR1027) as the chromogen.

Figure 1. Western blot analysis of ABCE1 using anti-ABCE1 antibody (AZQ6TNW3-1). 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-ABCE1 antigen affinity purified polyclonal antibody (AZQ6TNW3-1) 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 (AZQ6TNW3-1) .
ABCE1 was detected in a paraffin-embedded section of zebrafish brain tissue. The tissue section was incubated with rabbit anti-ABCE1 Antibody (AZQ6TNW3-1) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

Figure 3. IHC analysis of ABCE1 using anti-ABCE1 antibody (AZQ6TNW3-1) .
ABCE1 was detected in a paraffin-embedded section of zebrafish colon tissue. The tissue section was incubated with rabbit anti-ABCE1 Antibody (AZQ6TNW3-1) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

Figure 4. IHC analysis of ABCE1 using anti-ABCE1 antibody (AZQ6TNW3-1) .
ABCE1 was detected in a paraffin-embedded section of zebrafish kidney tissue. The tissue section was incubated with rabbit anti-ABCE1 Antibody (AZQ6TNW3-1) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

Figure 5. IHC analysis of ABCE1 using anti-ABCE1 antibody (AZQ6TNW3-1) .
ABCE1 was detected in a paraffin-embedded section of zebrafish retina tissue. The tissue section was incubated with rabbit anti-ABCE1 Antibody (AZQ6TNW3-1) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

Figure 1. Western blot analysis of ACADM using anti-ACADM antibody (AZA2CG95). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: zebrafish head tissue lysates,
Lane 2: female zebrafish viscera tissue lysates,
Lane 3: male zebrafish viscera tissue lysates,
Lane 4: whole zebrafish tissue lysates,
Lane 5: zebrafish embryo tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ACADM antigen affinity purified polyclonal antibody (AZA2CG95) 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 ACADM at approximately 43 kDa. The expected band size for ACADM is at 47 kDa.

Figure 1. Western blot analysis of ACADM using anti-ACADM antibody (AZA2CG95-1). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: zebrafish head tissue lysates,
Lane 2: female zebrafish viscera tissue lysates,
Lane 3: male zebrafish viscera tissue lysates,
Lane 4: whole zebrafish tissue lysates,
Lane 5: zebrafish embryo tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ACADM antigen affinity purified polyclonal antibody (AZA2CG95-1) 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 ACADM at approximately 43 kDa. The expected band size for ACADM is at 47 kDa.

Figure 1. Western blot analysis of ADRM1 using anti-ADRM1 antibody (AZQ6NZ09). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: zebrafish head tissue lysates,
Lane 2: female zebrafish viscera tissue lysates,
Lane 3: male zebrafish viscera tissue lysates,
Lane 4: whole zebrafish tissue lysates,
Lane 5: zebrafish embryo tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ADRM1 antigen affinity purified polyclonal antibody (AZQ6NZ09) 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 ADRM1 at approximately 42 kDa. The expected band size for ADRM1 is at 42 kDa.

Figure 2. IHC analysis of ADRM1 using anti-ADRM1 antibody (AZQ6NZ09) .
ADRM1 was detected in a paraffin-embedded section of zebrafish brain tissue. The tissue section was incubated with rabbit anti-ADRM1 Antibody (AZQ6NZ09) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

Figure 1. Western blot analysis of AFF4 using anti-AFF4 antibody (AZA0A8N7TEI3). 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-AFF4 antigen affinity purified polyclonal antibody (AZA0A8N7TEI3) 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 AFF4 at approximately 170 kDa. The expected band size for AFF4 is at 127 kDa.

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. Western blot analysis of AGO1 using anti-AGO1 antibody (AZK4I6K9). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: zebrafish head tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-AGO1 antigen affinity purified polyclonal antibody (AZK4I6K9) 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 AGO1 at approximately 97 kDa. The expected band size for AGO1 is at 97 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 # AR1027) as the chromogen.

Figure 1. Western blot analysis of AKT1/2/3 using anti-AKT1/2/3 antibody (AZQ802Y3). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: zebrafish head tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-AKT1/2/3 antigen affinity purified polyclonal antibody (AZQ802Y3) 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 AKT1/2/3 at approximately 62 kDa. The expected band size for AKT1/2/3 is at 56 kDa.

Figure 1. Western blot analysis of AKT3 using anti-AKT3 antibody (AZD9IL79). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: female zebrafish viscera tissue lysates,
Lane 2: male zebrafish viscera tissue lysates,
Lane 3: whole zebrafish tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-AKT3 antigen affinity purified polyclonal antibody (AZD9IL79) 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 AKT3 at approximately 56 kDa. The expected band size for AKT3 is at 56 kDa.

Figure 1. Western blot analysis of ALCAMA using anti-ALCAMA antibody (AZQ90460). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: zebrafish head tissue lysates.
Lane 2: whole female zebrafish tissue lysates.
Lane 3: whole male zebrafish tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ALCAMA antigen affinity purified polyclonal antibody (AZQ90460) 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 ALCAMA at approximately 95 kDa. The expected band size for ALCAMA is at 61 kDa.

Figure 2. IHC analysis of ALCAMA using anti-ALCAMA antibody (AZQ90460) .
ALCAMA was detected in a paraffin-embedded section of zebrafish brain tissue. The tissue section was incubated with rabbit anti-ALCAMA Antibody (AZQ90460) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

Figure 3. IHC analysis of ALCAMA using anti-ALCAMA antibody (AZQ90460) .
ALCAMA was detected in a paraffin-embedded section of zebrafish heart tissue. The tissue section was incubated with rabbit anti-ALCAMA Antibody (AZQ90460) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

Figure 4. IHC analysis of ALCAMA using anti-ALCAMA antibody (AZQ90460) .
ALCAMA was detected in a paraffin-embedded section of zebrafish liver tissue. The tissue section was incubated with rabbit anti-ALCAMA Antibody (AZQ90460) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

Figure 5. IHC analysis of ALCAMA using anti-ALCAMA antibody (AZQ90460) .
ALCAMA was detected in a paraffin-embedded section of zebrafish colon tissue. The tissue section was incubated with rabbit anti-ALCAMA Antibody (AZQ90460) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

Figure 6. IHC analysis of ALCAMA using anti-ALCAMA antibody (AZQ90460) .
ALCAMA was detected in a paraffin-embedded section of zebrafish muscle tissue. The tissue section was incubated with rabbit anti-ALCAMA Antibody (AZQ90460) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

Figure 7. IHC analysis of ALCAMA using anti-ALCAMA antibody (AZQ90460) .
ALCAMA was detected in a paraffin-embedded section of zebrafish kidney tissue. The tissue section was incubated with rabbit anti-ALCAMA Antibody (AZQ90460) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

Figure 1. IHC analysis of alk using anti-alk antibody (DZ41261) .
alk was detected in a paraffin-embedded section of zebrafish brain tissue. The tissue section was incubated with rabbit anti-alk Antibody (DZ41261) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.

Figure 1. Western blot analysis of Alpha Parvin/Actopaxin/PARVA using anti-Alpha Parvin/Actopaxin/PARVA antibody (AZQ6DRM4). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: zebrafish head tissue lysates,
Lane 2: female zebrafish viscera tissue lysates,
Lane 3: male zebrafish viscera tissue lysates,
Lane 4: whole female zebrafish tissue lysates,
Lane 5: whole male zebrafish tissue lysates,
Lane 6: zebrafish embryo tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Alpha Parvin/Actopaxin/PARVA antigen affinity purified polyclonal antibody (AZQ6DRM4) 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 Alpha Parvin/Actopaxin/PARVA at approximately 42 kDa. The expected band size for Alpha Parvin/Actopaxin/PARVA is at 42 kDa.

Figure 1. Western blot analysis of Androgen receptor/AR using anti-Androgen receptor/AR antibody (AZA4GT83). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: zebrafish head tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Androgen receptor/AR antigen affinity purified polyclonal antibody (AZA4GT83) 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 Androgen receptor/AR at approximately 96 kDa. The expected band size for Androgen receptor/AR is at 96 kDa.