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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 1. Western blot analysis of SELENOT using anti-SELENOT antibody (A31970). 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 A431 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: human T-47D whole cell lysates, Lane 6: human RT4 whole cell lysates, Lane 7: rat pancreas tissue lysates, Lane 8: mouse pancreas tissue lysates, Lane 9: mouse NIH/3T3 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-SELENOT antigen affinity purified polyclonal antibody (Catalog # A31970) 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 SELENOT at approximately 22 kDa. The expected band size for SELENOT is at 22 kDa.
Product group Antibodies
Boster Bio
Anti-SELENOT Antibody Picoband(r)A31970-CY3
TargetSELENOT
  • SizePrice
Figure 1. Western blot analysis of SELENOT using anti-SELENOT antibody (A31970). 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 A431 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: human T-47D whole cell lysates, Lane 6: human RT4 whole cell lysates, Lane 7: rat pancreas tissue lysates, Lane 8: mouse pancreas tissue lysates, Lane 9: mouse NIH/3T3 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-SELENOT antigen affinity purified polyclonal antibody (Catalog # A31970) 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 SELENOT at approximately 22 kDa. The expected band size for SELENOT is at 22 kDa.
Product group Antibodies
Boster Bio
Anti-SELENOT Antibody Picoband(r)A31970-DYLIGHT488
TargetSELENOT
  • SizePrice
Figure 1. Western blot analysis of SELENOT using anti-SELENOT antibody (A31970). 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 A431 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: human T-47D whole cell lysates, Lane 6: human RT4 whole cell lysates, Lane 7: rat pancreas tissue lysates, Lane 8: mouse pancreas tissue lysates, Lane 9: mouse NIH/3T3 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-SELENOT antigen affinity purified polyclonal antibody (Catalog # A31970) 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 SELENOT at approximately 22 kDa. The expected band size for SELENOT is at 22 kDa.
Product group Antibodies
Boster Bio
Anti-SELENOT Antibody Picoband(r)A31970-DYLIGHT550
TargetSELENOT
  • SizePrice
Figure 1. Western blot analysis of SELENOT using anti-SELENOT antibody (A31970). 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 A431 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: human T-47D whole cell lysates, Lane 6: human RT4 whole cell lysates, Lane 7: rat pancreas tissue lysates, Lane 8: mouse pancreas tissue lysates, Lane 9: mouse NIH/3T3 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-SELENOT antigen affinity purified polyclonal antibody (Catalog # A31970) 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 SELENOT at approximately 22 kDa. The expected band size for SELENOT is at 22 kDa.
Product group Antibodies
Boster Bio
Anti-SELENOT Antibody Picoband(r)A31970-DYLIGHT594
TargetSELENOT
  • SizePrice
Figure 1. Western blot analysis of SELENOT using anti-SELENOT antibody (A31970). 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 A431 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: human T-47D whole cell lysates, Lane 6: human RT4 whole cell lysates, Lane 7: rat pancreas tissue lysates, Lane 8: mouse pancreas tissue lysates, Lane 9: mouse NIH/3T3 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-SELENOT antigen affinity purified polyclonal antibody (Catalog # A31970) 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 SELENOT at approximately 22 kDa. The expected band size for SELENOT is at 22 kDa.
Product group Antibodies
Boster Bio
Anti-SELENOT Antibody Picoband(r)A31970-FITC
TargetSELENOT
  • SizePrice
Figure 1. Western blot analysis of SELENOT using anti-SELENOT antibody (A31970). 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 A431 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: human T-47D whole cell lysates, Lane 6: human RT4 whole cell lysates, Lane 7: rat pancreas tissue lysates, Lane 8: mouse pancreas tissue lysates, Lane 9: mouse NIH/3T3 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-SELENOT antigen affinity purified polyclonal antibody (Catalog # A31970) 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 SELENOT at approximately 22 kDa. The expected band size for SELENOT is at 22 kDa.
Product group Antibodies
Boster Bio
Anti-SELENOT Antibody Picoband(r)A31970-HRP
TargetSELENOT
  • SizePrice
Figure 1. Western blot analysis of SELENOT using anti-SELENOT antibody (A31970). 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 A431 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: human T-47D whole cell lysates, Lane 6: human RT4 whole cell lysates, Lane 7: rat pancreas tissue lysates, Lane 8: mouse pancreas tissue lysates, Lane 9: mouse NIH/3T3 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-SELENOT antigen affinity purified polyclonal antibody (Catalog # A31970) 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 SELENOT at approximately 22 kDa. The expected band size for SELENOT is at 22 kDa.
Product group Antibodies
Boster Bio
Anti-SELENOT Antibody Picoband(r)A31970-IFLUOR647
TargetSELENOT
  • SizePrice
Figure 1. Western blot analysis of SELENOT using anti-SELENOT antibody (A31970). 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 A431 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: human T-47D whole cell lysates, Lane 6: human RT4 whole cell lysates, Lane 7: rat pancreas tissue lysates, Lane 8: mouse pancreas tissue lysates, Lane 9: mouse NIH/3T3 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-SELENOT antigen affinity purified polyclonal antibody (Catalog # A31970) 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 SELENOT at approximately 22 kDa. The expected band size for SELENOT is at 22 kDa.
Product group Antibodies
Boster Bio
Anti-SELENOT Antibody Picoband(r)A31970-PE
TargetSELENOT
  • SizePrice
Figure 1. Western blot analysis of SELENOT using anti-SELENOT antibody (A31970). 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 A431 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: human T-47D whole cell lysates, Lane 6: human RT4 whole cell lysates, Lane 7: rat pancreas tissue lysates, Lane 8: mouse pancreas tissue lysates, Lane 9: mouse NIH/3T3 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-SELENOT antigen affinity purified polyclonal antibody (Catalog # A31970) 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 SELENOT at approximately 22 kDa. The expected band size for SELENOT is at 22 kDa.
Product group Antibodies
Boster Bio
Anti-SELENOT Antibody Picoband(r)A31970
TargetSELENOT
  • SizePrice
Figure 1. Western blot analysis of SELENON using anti-SELENON antibody (A31971-1). 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 A549 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Hela 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-SELENON antigen affinity purified polyclonal antibody (Catalog # A31971-1) 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 SELENON at approximately 66-70 kDa. The expected band size for SELENON is at 66-70 kDa.
Product group Antibodies
Boster Bio
Anti-SELENON Antibody Picoband(r)A31971-1-10UG
TargetSELENON
  • SizePrice
Figure 1. Western blot analysis of SELENON using anti-SELENON antibody (A31971-1). 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 A549 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Hela 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-SELENON antigen affinity purified polyclonal antibody (Catalog # A31971-1) 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 SELENON at approximately 66-70 kDa. The expected band size for SELENON is at 66-70 kDa.
Product group Antibodies
Boster Bio
Anti-SELENON Antibody Picoband(r)A31971-1-APC
TargetSELENON
  • SizePrice
Figure 1. Western blot analysis of SELENON using anti-SELENON antibody (A31971-1). 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 A549 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Hela 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-SELENON antigen affinity purified polyclonal antibody (Catalog # A31971-1) 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 SELENON at approximately 66-70 kDa. The expected band size for SELENON is at 66-70 kDa.
Product group Antibodies
Boster Bio
Anti-SELENON Antibody Picoband(r)A31971-1-BIOTIN
TargetSELENON
  • SizePrice
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