Western blot analysis of ABCD3 using anti-ABCD3 antibody (BA3339). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Rat Lung tissue lysates,
Lane 2: Rat Ovary tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ABCD3 antigen affinity purified polyclonal antibody (BA3339) 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 ABCD3 at approximately 74 kDa. The expected band size for ABCD3 is at 75 kDa.

IHC analysis of ABCD3 using anti-ABCD3 antibody (BA3339).
ABCD3 was detected in a paraffin-embedded section of human lung cancer tissue. The tissue section was incubated with rabbit anti-ABCD3 Antibody (BA3339) 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.

IHC analysis of ABCD3 using anti-ABCD3 antibody (BA3339).
ABCD3 was detected in a paraffin-embedded section of rat brain tissue. The tissue section was incubated with rabbit anti-ABCD3 Antibody (BA3339) 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.

Western blot analysis of ADRA2A using anti-ADRA2A antibody (BA3302-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: HELA whole cell lysates,
Lane 2: PANC whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ADRA2A antigen affinity purified polyclonal antibody (BA3302-2) 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 ADRA2A at approximately 55 kDa. The expected band size for ADRA2A is at 51 kDa.

Western blot analysis of APLN using anti-APLN antibody (BA3388-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: U87 whole cell lysates,
Lane 2: MCF-7 whole cell lysates,
Lane 3: HELA whole cell lysates,
Lane 4: MM453 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-APLN antigen affinity purified polyclonal antibody (BA3388-2) 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 APLN at approximately 9 kDa. The expected band size for APLN is at 9 kDa.

Western blot analysis of Alpha Antichymotrypsin/SERPINA3 using anti-Alpha Antichymotrypsin/SERPINA3 antibody (BA3355). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human SMMC whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Alpha Antichymotrypsin/SERPINA3 antigen affinity purified polyclonal antibody (BA3355) 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 Antichymotrypsin/SERPINA3 at approximately 50-60 kDa. The expected band size for Alpha Antichymotrypsin/SERPINA3 is at 48 kDa.

IHC analysis of Alpha Antichymotrypsin/SERPINA3 using anti-Alpha Antichymotrypsin/SERPINA3 antibody (BA3355).
Alpha Antichymotrypsin/SERPINA3 was detected in a paraffin-embedded section of human liver cancer tissue. The tissue section was incubated with rabbit anti-Alpha Antichymotrypsin/SERPINA3 Antibody (BA3355) 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.

Western blot analysis of BMPR1B using anti-BMPR1B antibody (BA3305).
Lane 1: recombinant Human BMPR1B Protein 10ng,
Lane 2: recombinant Human BMPR1B Protein 5ng,
Lane 3: recombinant Human BMPR1B Protein 2.5ng,
Lane 4: recombinant Human BMPR1B Protein 1.25ng.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-BMPR1B antigen affinity purified polyclonal antibody (BA3305) 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 BMPR1B at approximately 49 kDa.

Western blot analysis of Bcl-XS/BCL2L1 using anti-Bcl-XS/BCL2L1 antibody (BA3368). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: HELA whole cell lysates,
Lane 2: PC-12 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Bcl-XS/BCL2L1 antigen affinity purified polyclonal antibody (BA3368) 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 Bcl-XS/BCL2L1 at approximately 26 kDa、19 kDa. The expected band size for Bcl-XS/BCL2L1 is at 26 kDa.

IHC analysis of Bcl-XS/BCL2L1 using anti-Bcl-XS/BCL2L1 antibody (BA3368).
Bcl-XS/BCL2L1 was detected in a paraffin-embedded section of human colon cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Bcl-XS/BCL2L1 Antibody (BA3368) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.

Western blot analysis of CD90/THY1 using anti-CD90/THY1 antibody (BA3391). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human Hela whole cell lysates,
Lane 2: human Jurkat whole cell lysates,
Lane 3: human HT1080 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-CD90/THY1 antigen affinity purified polyclonal antibody (BA3391) 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 CD90/THY1 at approximately 22-30 kDa. The expected band size for CD90/THY1 is at 18 kDa.

IHC analysis of CD90/THY1 using anti-CD90/THY1 antibody (BA3391).
CD90/THY1 was detected in a paraffin-embedded section of human lung cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-CD90/THY1 Antibody (BA3391) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.

Western blot analysis of CUL4B using anti-CUL4B antibody (BA3374-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human Hela whole cell lysates,
Lane 2: human A549 whole cell lysates,
Lane 3: rat thymus tissue lysates,
Lane 4: rat kidney tissue lysates,
Lane 5: mouse kidney tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-CUL4B antigen affinity purified polyclonal antibody (BA3374-2) 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 CUL4B at approximately 104 kDa. The expected band size for CUL4B is at 104 kDa.

IHC analysis of CUL4B using anti-CUL4B antibody (BA3374-2).
CUL4B was detected in a paraffin-embedded section of zebrafish body tissue. The tissue section was incubated with rabbit anti-CUL4B Antibody (BA3374-2) 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.

Western blot analysis of Caspase 6/CASP6 (p18) using anti-Caspase 6/CASP6 (p18) antibody (BA3328). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Rat Liver tissue lysates,
Lane 2: Rat Kidney tissue lysates,
Lane 3: Rat Testis tissue lysates,
Lane 4: NRK whole cell lysates,
Lane 5: Mouse Liver tissue lysates,
Lane 6: Mouse Kidney tissue lysates,
Lane 7: Mouse Testis tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Caspase 6/CASP6 (p18) antigen affinity purified polyclonal antibody (BA3328) 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 Caspase 6/CASP6 (p18) at approximately 33 kDa. The expected band size for Caspase 6/CASP6 (p18) is at 32 kDa.

IHC analysis of Caspase 6/CASP6 (p18) using anti-Caspase 6/CASP6 (p18) antibody (BA3328).
Caspase 6/CASP6 (p18) was detected in a paraffin-embedded section of rat spleen tissue. The tissue section was incubated with rabbit anti-Caspase 6/CASP6 (p18) Antibody (BA3328) 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.

IHC analysis of Caspase 6/CASP6 (p18) using anti-Caspase 6/CASP6 (p18) antibody (BA3328).
Caspase 6/CASP6 (p18) was detected in a paraffin-embedded section of rat intestine tissue. The tissue section was incubated with rabbit anti-Caspase 6/CASP6 (p18) Antibody (BA3328) 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.

IHC analysis of Caspase 6/CASP6 (p18) using anti-Caspase 6/CASP6 (p18) antibody (BA3328).
Caspase 6/CASP6 (p18) was detected in a paraffin-embedded section of mouse lung tissue. The tissue section was incubated with rabbit anti-Caspase 6/CASP6 (p18) Antibody (BA3328) 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.

IHC analysis of Caspase 6/CASP6 (p18) using anti-Caspase 6/CASP6 (p18) antibody (BA3328).
Caspase 6/CASP6 (p18) was detected in frozen section of rat spleen tissue. The tissue section was incubated with rabbit anti-Caspase 6/CASP6 (p18) Antibody (BA3328) 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.

Western blot analysis of FANK1 using anti-FANK1 antibody (BA3322). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human A431 whole cell lysates,
Lane 2: human Hacat whole cell lysates,
Lane 3: human MCF-7 whole cell lysates,
Lane 4: rat testis tissue lysates,
Lane 5: mouse testis tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-FANK1 antigen affinity purified polyclonal antibody (BA3322) 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 FANK1 at approximately 38 kDa. The expected band size for FANK1 is at 38 kDa.

IHC analysis of FANK1 using anti-FANK1 antibody (BA3322) .
FANK1 was detected in a paraffin-embedded section of rat testis tissue. The tissue section was incubated with rabbit anti-FANK1 Antibody (BA3322) 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.

Western blot analysis of FBXL4 using anti-FBXL4 antibody (BA3358). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Rat Liver tissue lysates,
Lane 2: Rat Lung tissue lysates,
Lane 3: HELA whole cell lysates,
Lane 4: PANC whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-FBXL4 antigen affinity purified polyclonal antibody (BA3358) 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 FBXL4 at approximately 70 kDa. The expected band size for FBXL4 is at 70 kDa.

IHC analysis of FBXL4 using anti-FBXL4 antibody (BA3358).
FBXL4 was detected in a paraffin-embedded section of human lung cancer tissue. The tissue section was incubated with rabbit anti-FBXL4 Antibody (BA3358) 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.

Western blot analysis of GLI2 using anti-GLI2 antibody (BA3326-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human placenta tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-GLI2 antigen affinity purified polyclonal antibody (BA3326-2) 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 GLI2 at approximately 180-200 kDa. The expected band size for GLI2 is at 168 kDa.

Western blot analysis of GLI2 using anti-GLI2 antibody (BA3326-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: MCF-7 whole cell lysates,
Lane 2: HELA whole cell lysates,
Lane 3: SKOV whole cell lysates,
Lane 4: HT1080 whole cell lysates,
Lane 5: A549 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-GLI2 antigen affinity purified polyclonal antibody (BA3326-2) 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 GLI2 at approximately 180-200 kDa. The expected band size for GLI2 is at 168 kDa.

Western blot analysis of GLUR3 using anti-GLUR3 antibody (BA3396). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: Rat brain tissue lysates,
Lane 2: Mouse brain tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-GLUR3 antigen affinity purified polyclonal antibody (BA3396) 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 GLUR3 at approximately 101 kDa. The expected band size for GLUR3 is at 101 kDa.

IHC analysis of Gremlin/GREM1 using anti-Gremlin/GREM1 antibody (BA3387).
Gremlin/GREM1 was detected in a paraffin-embedded section of human breast cancer tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-Gremlin/GREM1 Antibody (BA3387) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.

IHC analysis of HAS2 using anti-HAS2 antibody (BA3397-1).
HAS2 was detected in a paraffin-embedded section of human placenta tissue. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The tissue section was incubated with rabbit anti-HAS2 Antibody (BA3397-1) at a dilution of 1:200 and developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.

Western blot analysis of HSD17B1 using anti-HSD17B1 antibody (BA3399). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human T47D whole cell lysates,
Lane 2: human 293T whole cell lysates,
Lane 3: rat C6 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-HSD17B1 antigen affinity purified polyclonal antibody (BA3399) 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 HSD17B1 at approximately 37 kDa. The expected band size for HSD17B1 is at 35 kDa.

IHC analysis of HSD17B1 using anti-HSD17B1 antibody (BA3399).
HSD17B1 was detected in a paraffin-embedded section of rat liver tissue. The tissue section was incubated with rabbit anti-HSD17B1 Antibody (BA3399) 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.

IHC analysis of HSD17B1 using anti-HSD17B1 antibody (BA3399).
HSD17B1 was detected in a paraffin-embedded section of rat ovary tissue. The tissue section was incubated with rabbit anti-HSD17B1 Antibody (BA3399) 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.

IHC analysis of HSD17B1 using anti-HSD17B1 antibody (BA3399).
HSD17B1 was detected in a paraffin-embedded section of human placenta tissue. The tissue section was incubated with rabbit anti-HSD17B1 Antibody (BA3399) 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.

ICC analysis of HSD17B1 using anti- HSD17B1 antibody (BA3399).
HSD17B1 was detected in an immunocytochemical section of Hela cells. The section was incubated with rabbit anti-HSD17B1 Antibody (BA3399) at a dilution of 1:100. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.

Western blot analysis of IFN Gamma/IFNG using anti-IFN Gamma/IFNG antibody (BA3383-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: rat thymus tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-IFN Gamma/IFNG antigen affinity purified polyclonal antibody (BA3383-2) 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 IFN Gamma/IFNG at approximately 19 kDa. The expected band size for IFN Gamma/IFNG is at 18 kDa.

Western blot analysis of ITGA7 using anti-ITGA7 antibody (BA3357-2). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: 293T whole cell lysates,
Lane 2: A431 whole cell lysates,
Lane 3: HELA whole cell lysates,
Lane 4: JURKAT whole cell lysates,
Lane 5: RAJI whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ITGA7 antigen affinity purified polyclonal antibody (BA3357-2) 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 ITGA7 at approximately 130 kDa. The expected band size for ITGA7 is at 129 kDa.

Western blot analysis of Integrin Alpha 6/ITGA6 using anti-Integrin Alpha 6/ITGA6 antibody (BA3356). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human 293T whole cell lysates,
Lane 2: human A431 whole cell lysates,
Lane 3: human Hela whole cell lysates,
Lane 4: human Jurkat whole cell lysates,
Lane 5: human Raji whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Integrin Alpha 6/ITGA6 antigen affinity purified polyclonal antibody (BA3356) 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 Integrin Alpha 6/ITGA6 at approximately 127 kDa. The expected band size for Integrin Alpha 6/ITGA6 is at 127 kDa.

ICC analysis of Integrin Alpha 6/ITGA6 using anti-Integrin Alpha 6/ITGA6 antibody (BA3356).
Integrin Alpha 6/ITGA6 was detected in an immunocytochemical section of Hela cells. The section was incubated with rabbit anti-Integrin Alpha 6/ITGA6 Antibody (BA3356) at a dilution of 1:100. Biotinylated goat anti-rabbit IgG was used as secondary antibody. The section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB (Catalog # AR1027) as the chromogen.