Western blot analysis of anti-14-3-3 alpha/beta antibody (BM4752). 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 Caco-2 whole cell lysates,
Lane 3: human SiHa whole cell lysates,
Lane 4: human Hacat whole cell lysates,
Lane 5: rat brain tissue lysates,
Lane 6: rat lung tissue lysates,
Lane 7: mouse brain tissue lysates,
Lane 8: mouse lung tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-14-3-3 alpha/beta antigen affinity purified monoclonal antibody (BM4752) 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 14-3-3 alpha/beta at approximately 28 kDa. The expected band size for 14-3-3 alpha/beta is at 28 kDa.

Western blot analysis of ASPP2 expression in MCF7 cell lysate.

Western blot analysis of anti-ACC1/ACACA antibody (BM4414). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human HepG2 whole cell lysates,
Lane 2: rat liver tissue lysates,
Lane 3: mouse liver tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ACC1/ACACA antigen affinity purified monoclonal antibody (BM4414) 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 ACC1/ACACA at approximately 266 kDa. The expected band size for ACC1/ACACA is at 266 kDa.

Immunohistochemical analysis of paraffin-embedded human kidney, using Acetyl-CoA Carboxylase Antibody.

Western blot analysis of ACE2 expression in Human kidney lysate.

Western blot analysis of ADIPOR1 expression in Human heart lysate.

Immunohistochemical analysis of paraffin-embedded human kidney, using ADIPOR1 Antibody.

All lanes use the Antibody for 1 hour at room temperature.

All lanes use the Antibody for 1 hour at room temperature.

Western blot analysis of AFP expression in HepG2 cell lysate.

All lanes use the Antibody for 1 hour at room temperature.

Western blot analysis of anti-AGO2 antibody (BM4920). 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 K562 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-AGO2 antigen affinity purified monoclonal antibody (BM4920) 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 AGO2 at approximately 97 kDa. The expected band size for AGO2 is at 97 kDa.

Western blot analysis of AGTR1 expression in (1) HeLa cell lysate; (2) PC-12 cell lysate.

Western blot analysis of anti-AGTR2 antibody (BM4557). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human HepG2 whole cell lysates,
Lane 2: human SH-SY5Y whole cell lysates,
Lane 3: human Caco-2 whole cell lysates,
Lane 4: rat lung tissue lysates,
Lane 5: mouse lung tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-AGTR2 antigen affinity purified monoclonal antibody (BM4557) 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 AGTR2 at approximately 45 kDa. The expected band size for AGTR2 is at 41 kDa.

Western blot analysis of anti-AHR antibody (BM4965). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human RT4 whole cell lysates,
Lane 2: human U-87MG whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-AHR antigen affinity purified monoclonal antibody (BM4965) 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 AHR at approximately 96, 105 kDa. The expected band size for AHR is at 96 kDa.

Western blot analysis of anti- AKT1 antibody (BM4390). The sample well of each lane was loaded with 50ug of sample under reducing conditions.
Lane 1: HEPG2 whole cell lysates,
Lane 2: A549 whole cell lysates,
Lane 3: HELA whole cell lysates,
Lane 4: Raji whole cell lysates,
Lane 5: MCF-7 whole cell lysates,
Lane 6: SIHA whole cell lysates,
Lane 7: 293T whole cell lysates.
Use rabbit Anti-AKT1 1:1000, probed with a goat Anti-rabbit IgG-HRP secondary antibody. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002). A specific band was detected for AKT1 at approximately 60KD. The expected band size for AKT1 is at 56KD.

Western blot analysis of anti- AKT1 antibody (BM4390). The sample well of each lane was loaded with 50ug of sample under reducing conditions.
Lane 1: rat liver tissue lysates,
Lane 2: rat brain tissue lysates,
Lane 3: C6 whole cell lysates,
Lane 4: RH35 whole cell lysates,
Lane 5:mouse liver tissue lysates,
Lane 6: mouse brain tissue lysates,
Lane 7: Neuro-2a whole cell lysates.
Lane 8: HEPA1-6 whole cell lysates.
Use rabbit Anti-AKT1 1:1000, probed with a goat Anti-rabbit IgG-HRP secondary antibody. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002). A specific band was detected for AKT1 at approximately 60KD. The expected band size for AKT1 is at 56KD.

Western blot analysis of AKT1/2 expression in (1) HeLa cell lysate; (2) NIH/3T3 cell lysate.

All lanes use the Antibody for 1 hour at room temperature.

All lanes use the Antibody for 1 hour at room temperature.

Western blot analysis of anti-AKT1/2/3 antibody (BM4400). 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: human 293T whole cell lysates,
Lane 4: human U2OS whole cell lysates,
Lane 5: rat brain tissue lysates,
Lane 6: rat heart tissue lysates,
Lane 7: mouse brain tissue lysates,
Lane 8: mouse heart tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-AKT1/2/3 antigen affinity purified monoclonal antibody (BM4400) 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 60 kDa. The expected band size for AKT1/2/3 is at 60 kDa.

Immunohistochemical analysis of paraffin-embedded human testis, using Akt(pan)1/2/3 Antibody.

Immunohistochemical analysis of paraffin-embedded Human pituitary tumor, using the Antibody.

Immunohistochemical analysis of paraffin-embedded Human ovarian cancer, using the Antibody.

Immunohistochemical analysis of paraffin-embedded Human astrocytoma, using the Antibody.

Immunofluorescent analysis of MCF-7 cells, using Akt(pan)1/2/3 Antibody.

Immunoprecipitate (IP) analysis using the Antibody. (wb)

Western blot analysis of anti-ALDH1A1 antibody (BM4034). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human HepG2 whole cell lysates,
Lane 2: human A549 whole cell lysates,
Lane 3: rat kidney tissue lysates,
Lane 4: mouse liver tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ALDH1A1 antigen affinity purified monoclonal antibody (BM4034) 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 ALDH1A1 at approximately 50 kDa. The expected band size for ALDH1A1 is at 55 kDa.

Immunohistochemical analysis of paraffin-embedded human liver cancer, using ALDH1A1 Antibody.

Immunohistochemical analysis of paraffin-embedded human liver, using Alkaline Phosphatase Antibody.

Immunofluorescent analysis of Hela cells, using Alkaline Phosphatase Antibody .

Western blot analysis of anti-ALPL antibody (BM4284). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human HepG2 whole cell lysates,
Lane 2: human Jurkat whole cell lysates,
Lane 3: human MCF-7 whole cell lysates,
Lane 4: human K562 whole cell lysates,
Lane 5: rat liver tissue lysates,
Lane 6: rat spleen tissue lysates,
Lane 7: mouse liver tissue lysates,
Lane 8: mouse spleen tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ALPL antigen affinity purified monoclonal antibody (BM4284) at a dilution of 1:2000 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 ALPL at approximately 80 kDa. The expected band size for ALPL is at 57 kDa.

Western blot analysis of anti-AMPK Alpha 1/PRKAA1 antibody (BM4202). 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 U-87 MG whole cell lysates,
Lane 3: human PC-3 whole cell lysates,
Lane 4: rat PC-12 whole cell lysates,
Lane 5: rat RH-35 whole cell lysates,
Lane 6: mouse RAW264.7 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-AMPK Alpha 1/PRKAA1 antigen affinity purified monoclonal antibody (BM4202) 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 AMPK Alpha 1/PRKAA1 at approximately 64 kDa. The expected band size for AMPK Alpha 1/PRKAA1 is at 64 kDa.

Immunohistochemical analysis of paraffin-embedded Human lung adenocarcinoma, using the Antibody.

Immunohistochemical analysis of paraffin-embedded Human tonsil, using the Antibody.

Immunohistochemical analysis of paraffin-embedded Human pituitary tumor, using the Antibody.

Immunohistochemical analysis of paraffin-embedded human kidney, using AMPK alpha 1 Antibody.

Immunofluorescent analysis of Hela cells, using AMPK alpha 1 Antibody.

Western blot analysis of anti-ARID1A antibody (BM4822). 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 A375 whole cell lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ARID1A antigen affinity purified monoclonal antibody (BM4822) 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 ARID1A at approximately 270 kDa. The expected band size for ARID1A is at 242 kDa.

Immunohistochemical analysis of paraffin-embedded human adenocarcinoma of colon, using ARID1A Antibody.

Immunofluorescent analysis of SH-SY5Y cells, using ARID1A Antibody.

Western blot analysis of p16 Arc expression in Human fetal brain lysate.

Immunohistochemical analysis of paraffin-embedded human colon, using p16 ARC Antibody.

All lanes use the Antibody for 1 hour at room temperature.

All lanes use the Antibody for 1 hour at room temperature.

Western blot analysis of anti-ASK1/MAP3K5 antibody (BM4220). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human RT4 whole cell lysates,
Lane 2: human HEL whole cell lysates,
Lane 3: human SIHA whole cell lysates,
Lane 4: mouse heart tissue lysates,
Lane 5: mouse lung tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ASK1/MAP3K5 antigen affinity purified monoclonal antibody (BM4220) 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 ASK1/MAP3K5 at approximately 155 kDa. The expected band size for ASK1/MAP3K5 is at 155 kDa.

IHC analysis of ASK1/MAP3K5 using anti-ASK1/MAP3K5 antibody (BM4220) .
ASK1/MAP3K5 was detected in a paraffin-embedded section of human liver cancer tissue. The tissue section was incubated with rabbit anti-ASK1/MAP3K5 Antibody (BM4220) 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 ASK1/MAP3K5 using anti-ASK1/MAP3K5 antibody (BM4220) .
ASK1/MAP3K5 was detected in a paraffin-embedded section of human liver cancer tissue. The tissue section was incubated with rabbit anti-ASK1/MAP3K5 Antibody (BM4220) 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 ASK1/MAP3K5 using anti-ASK1/MAP3K5 antibody (BM4220) .
ASK1/MAP3K5 was detected in a paraffin-embedded section of human placenta tissue. The tissue section was incubated with rabbit anti-ASK1/MAP3K5 Antibody (BM4220) 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 ASK1/MAP3K5 using anti-ASK1/MAP3K5 antibody (BM4220) .
ASK1/MAP3K5 was detected in a paraffin-embedded section of human placenta tissue. The tissue section was incubated with rabbit anti-ASK1/MAP3K5 Antibody (BM4220) 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 ASK1/MAP3K5 using anti-ASK1/MAP3K5 antibody (BM4220) .
ASK1/MAP3K5 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. The tissue section was incubated with rabbit anti-ASK1/MAP3K5 Antibody (BM4220) 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 ASK1/MAP3K5 using anti-ASK1/MAP3K5 antibody (BM4220) .
ASK1/MAP3K5 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. The tissue section was incubated with rabbit anti-ASK1/MAP3K5 Antibody (BM4220) 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 ASK1/MAP3K5 using anti-ASK1/MAP3K5 antibody (BM4220) .
ASK1/MAP3K5 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. The tissue section was incubated with rabbit anti-ASK1/MAP3K5 Antibody (BM4220) 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 ASK1/MAP3K5 using anti-ASK1/MAP3K5 antibody (BM4220) .
ASK1/MAP3K5 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. The tissue section was incubated with rabbit anti-ASK1/MAP3K5 Antibody (BM4220) 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.

Immunofluorescent analysis using the Antibody.

Western blot analysis of anti-ATF5 antibody (BM4714). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human Jurkat whole cell lysates,
Lane 2: human K562 whole cell lysates,
Lane 3: human THP-1 whole cell lysates,
Lane 4: rat liver tissue lysates,
Lane 5: mouse liver tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ATF5 antigen affinity purified monoclonal antibody (BM4714) 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 ATF5 at approximately 35 kDa. The expected band size for ATF5 is at 31 kDa.

IHC analysis of ATF5 using anti-ATF5 antibody (BM4714) .
ATF5 was detected in a paraffin-embedded section of human pancreas cancer tissue. The tissue section was incubated with rabbit anti-ATF5 Antibody (BM4714) 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 ATF5 using anti-ATF5 antibody (BM4714) .
ATF5 was detected in a paraffin-embedded section of mouse liver tissue. The tissue section was incubated with rabbit anti-ATF5 Antibody (BM4714) 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.