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Antibodies

We offer one of the most comprehensive portfolios of antibodies. This includes monoclonal and polyclonal primary, secondary, conjugated, phospho-specific, functional, (isotype) controls, tagged and antibody pairs. In addition, we offer custom antibody services from several manufacturers.

The antibodies are generated in various hosts and react to antigens of different species like human, mouse, rat, rabbit or zebrafish. The antibodies are validated for multiple applications, including immunohistochemistry, western blot, immunoprecipitation, ELISA and flow cytometry, to ensure reliable performance for your research needs.

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Figure 2. Immunohistochemistry validation of TRIP13 using Anti-TRIP13 Antibody (A06921-1). Immunohistochemistry (IHC) analyzes of TRIP13 pAb in paraffin-embedded human lung carcinoma tissue at 1:50.showing cytoplasmic and nucleus staining. Negative control (the right)Using PBS instead of primary antibody
Product group Antibodies
Boster Bio
Anti-TRIP13 AntibodyA06921-1
ApplicationsWestern Blot, ImmunoHistoChemistry
ReactivityHuman, Mouse, Rat
TargetTRIP13
  • SizePrice
Figure 1. Western blot analysis of PCH2/TRIP13 using anti-PCH2/TRIP13 antibody (A06921-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. 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 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCH2/TRIP13 antigen affinity purified polyclonal antibody (Catalog # A06921-2) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCH2/TRIP13 at approximately 49 kDa. The expected band size for PCH2/TRIP13 is at 49 kDa.
Product group Antibodies
Boster Bio
Anti-PCH2/TRIP13 Antibody Picoband(r)A06921-2-10UG
ApplicationsFlow Cytometry, Western Blot, ELISA
ReactivityHuman
TargetTRIP13
  • SizePrice
Figure 1. Western blot analysis of PCH2/TRIP13 using anti-PCH2/TRIP13 antibody (A06921-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. 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 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCH2/TRIP13 antigen affinity purified polyclonal antibody (Catalog # A06921-2) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCH2/TRIP13 at approximately 49 kDa. The expected band size for PCH2/TRIP13 is at 49 kDa.
Product group Antibodies
Boster Bio
Anti-PCH2/TRIP13 Antibody Picoband(r)A06921-2-APC
ApplicationsFlow Cytometry, Western Blot, ELISA
ReactivityHuman
TargetTRIP13
  • SizePrice
Figure 1. Western blot analysis of PCH2/TRIP13 using anti-PCH2/TRIP13 antibody (A06921-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. 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 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCH2/TRIP13 antigen affinity purified polyclonal antibody (Catalog # A06921-2) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCH2/TRIP13 at approximately 49 kDa. The expected band size for PCH2/TRIP13 is at 49 kDa.
Product group Antibodies
Boster Bio
Anti-PCH2/TRIP13 Antibody Picoband(r)A06921-2-BIOTIN
ApplicationsFlow Cytometry, Western Blot, ELISA
ReactivityHuman
TargetTRIP13
  • SizePrice
Figure 1. Western blot analysis of PCH2/TRIP13 using anti-PCH2/TRIP13 antibody (A06921-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. 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 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCH2/TRIP13 antigen affinity purified polyclonal antibody (Catalog # A06921-2) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCH2/TRIP13 at approximately 49 kDa. The expected band size for PCH2/TRIP13 is at 49 kDa.
Product group Antibodies
Boster Bio
Anti-PCH2/TRIP13 Antibody Picoband(r)A06921-2-CARRIER-FREE
ApplicationsFlow Cytometry, Western Blot, ELISA
ReactivityHuman
TargetTRIP13
  • SizePrice
Figure 1. Western blot analysis of PCH2/TRIP13 using anti-PCH2/TRIP13 antibody (A06921-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. 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 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCH2/TRIP13 antigen affinity purified polyclonal antibody (Catalog # A06921-2) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCH2/TRIP13 at approximately 49 kDa. The expected band size for PCH2/TRIP13 is at 49 kDa.
Product group Antibodies
Boster Bio
Anti-PCH2/TRIP13 Antibody Picoband(r)A06921-2-CY3
ApplicationsFlow Cytometry, Western Blot, ELISA
ReactivityHuman
TargetTRIP13
  • SizePrice
Figure 1. Western blot analysis of PCH2/TRIP13 using anti-PCH2/TRIP13 antibody (A06921-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. 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 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCH2/TRIP13 antigen affinity purified polyclonal antibody (Catalog # A06921-2) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCH2/TRIP13 at approximately 49 kDa. The expected band size for PCH2/TRIP13 is at 49 kDa.
Product group Antibodies
Boster Bio
Anti-PCH2/TRIP13 Antibody Picoband(r)A06921-2-DYLIGHT488
ApplicationsFlow Cytometry, Western Blot, ELISA
ReactivityHuman
TargetTRIP13
  • SizePrice
Figure 1. Western blot analysis of PCH2/TRIP13 using anti-PCH2/TRIP13 antibody (A06921-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. 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 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCH2/TRIP13 antigen affinity purified polyclonal antibody (Catalog # A06921-2) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCH2/TRIP13 at approximately 49 kDa. The expected band size for PCH2/TRIP13 is at 49 kDa.
Product group Antibodies
Boster Bio
Anti-PCH2/TRIP13 Antibody Picoband(r)A06921-2-DYLIGHT550
ApplicationsFlow Cytometry, Western Blot, ELISA
ReactivityHuman
TargetTRIP13
  • SizePrice
Figure 1. Western blot analysis of PCH2/TRIP13 using anti-PCH2/TRIP13 antibody (A06921-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. 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 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCH2/TRIP13 antigen affinity purified polyclonal antibody (Catalog # A06921-2) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCH2/TRIP13 at approximately 49 kDa. The expected band size for PCH2/TRIP13 is at 49 kDa.
Product group Antibodies
Boster Bio
Anti-PCH2/TRIP13 Antibody Picoband(r)A06921-2-DYLIGHT594
ApplicationsFlow Cytometry, Western Blot, ELISA
ReactivityHuman
TargetTRIP13
  • SizePrice
Figure 1. Western blot analysis of PCH2/TRIP13 using anti-PCH2/TRIP13 antibody (A06921-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. 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 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCH2/TRIP13 antigen affinity purified polyclonal antibody (Catalog # A06921-2) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCH2/TRIP13 at approximately 49 kDa. The expected band size for PCH2/TRIP13 is at 49 kDa.
Product group Antibodies
Boster Bio
Anti-PCH2/TRIP13 Antibody Picoband(r)A06921-2-FITC
ApplicationsFlow Cytometry, Western Blot, ELISA
ReactivityHuman
TargetTRIP13
  • SizePrice
Figure 1. Western blot analysis of PCH2/TRIP13 using anti-PCH2/TRIP13 antibody (A06921-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. 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 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCH2/TRIP13 antigen affinity purified polyclonal antibody (Catalog # A06921-2) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCH2/TRIP13 at approximately 49 kDa. The expected band size for PCH2/TRIP13 is at 49 kDa.
Product group Antibodies
Boster Bio
Anti-PCH2/TRIP13 Antibody Picoband(r)A06921-2-HRP
ApplicationsFlow Cytometry, Western Blot, ELISA
ReactivityHuman
TargetTRIP13
  • SizePrice
Figure 1. Western blot analysis of PCH2/TRIP13 using anti-PCH2/TRIP13 antibody (A06921-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. 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 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCH2/TRIP13 antigen affinity purified polyclonal antibody (Catalog # A06921-2) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCH2/TRIP13 at approximately 49 kDa. The expected band size for PCH2/TRIP13 is at 49 kDa.
Product group Antibodies
Boster Bio
Anti-PCH2/TRIP13 Antibody Picoband(r)A06921-2-IFLUOR647
ApplicationsFlow Cytometry, Western Blot, ELISA
ReactivityHuman
TargetTRIP13
  • SizePrice
148149150151152

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