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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 PRAG1 using anti-PRAG1 antibody (A32113). 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 Caco-2 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-PRAG1 antigen affinity purified polyclonal antibody (Catalog # A32113) 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 PRAG1 at approximately 200 kDa. The expected band size for PRAG1 is at 150 kDa.
Product group Antibodies
Boster Bio
Anti-PRAG1 Antibody Picoband(r)A32113-DYLIGHT550
TargetPRAG1
  • SizePrice
Figure 1. Western blot analysis of PRAG1 using anti-PRAG1 antibody (A32113). 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 Caco-2 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-PRAG1 antigen affinity purified polyclonal antibody (Catalog # A32113) 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 PRAG1 at approximately 200 kDa. The expected band size for PRAG1 is at 150 kDa.
Product group Antibodies
Boster Bio
Anti-PRAG1 Antibody Picoband(r)A32113-DYLIGHT594
TargetPRAG1
  • SizePrice
Figure 1. Western blot analysis of PRAG1 using anti-PRAG1 antibody (A32113). 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 Caco-2 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-PRAG1 antigen affinity purified polyclonal antibody (Catalog # A32113) 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 PRAG1 at approximately 200 kDa. The expected band size for PRAG1 is at 150 kDa.
Product group Antibodies
Boster Bio
Anti-PRAG1 Antibody Picoband(r)A32113-FITC
TargetPRAG1
  • SizePrice
Figure 1. Western blot analysis of PRAG1 using anti-PRAG1 antibody (A32113). 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 Caco-2 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-PRAG1 antigen affinity purified polyclonal antibody (Catalog # A32113) 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 PRAG1 at approximately 200 kDa. The expected band size for PRAG1 is at 150 kDa.
Product group Antibodies
Boster Bio
Anti-PRAG1 Antibody Picoband(r)A32113-HRP
TargetPRAG1
  • SizePrice
Figure 1. Western blot analysis of PRAG1 using anti-PRAG1 antibody (A32113). 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 Caco-2 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-PRAG1 antigen affinity purified polyclonal antibody (Catalog # A32113) 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 PRAG1 at approximately 200 kDa. The expected band size for PRAG1 is at 150 kDa.
Product group Antibodies
Boster Bio
Anti-PRAG1 Antibody Picoband(r)A32113-IFLUOR647
TargetPRAG1
  • SizePrice
Figure 1. Western blot analysis of PRAG1 using anti-PRAG1 antibody (A32113). 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 Caco-2 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-PRAG1 antigen affinity purified polyclonal antibody (Catalog # A32113) 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 PRAG1 at approximately 200 kDa. The expected band size for PRAG1 is at 150 kDa.
Product group Antibodies
Boster Bio
Anti-PRAG1 Antibody Picoband(r)A32113-PE
TargetPRAG1
  • SizePrice
Figure 1. Western blot analysis of PRAG1 using anti-PRAG1 antibody (A32113). 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 Caco-2 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-PRAG1 antigen affinity purified polyclonal antibody (Catalog # A32113) 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 PRAG1 at approximately 200 kDa. The expected band size for PRAG1 is at 150 kDa.
Product group Antibodies
Boster Bio
Anti-PRAG1 Antibody Picoband(r)A32113
TargetPRAG1
  • SizePrice
Figure 1. Western blotting validation for Anti-Phospho-Pragmin (Y413) PRAG1 Antibody A32113Y413 Western Blot (WB) analysis of A549 cells using Phospho-Pragmin (Y413) polyclonal antibody. Electrophoresis was performed on a SDS-PAGE gel. To determine SDS-PAGE gel concentration
Product group Antibodies
Boster Bio
Anti-Phospho-Pragmin (Y413) PRAG1 AntibodyA32113Y413
TargetPRAG1
  • SizePrice
Figure 1. Western blotting validation for Anti-MINA RIOX2 Antibody A32122-1 Western blot (WB) analysis of MINA polyclonal antibody at 1:500 dilution Lane1:HEK293T whole cell lysate Lane2:NIH-3T3 whole cell lysate Lane3:PC12 whole cell lysate Electrophoresis was performed on a SDS-PAGE gel. To determine SDS-PAGE gel concentration
Product group Antibodies
Boster Bio
Anti-MINA RIOX2 AntibodyA32122-1
TargetRIOX2
  • SizePrice
Figure 1. Western blotting validation for Anti-MINA53 RIOX2 Antibody A32122-2 Western blot analysis of MINA53 on PC-12 cells lysates using anti-MINA53 antibody at 1/500 dilution. Electrophoresis was performed on a SDS-PAGE gel. To determine SDS-PAGE gel concentration
Product group Antibodies
Boster Bio
Anti-MINA53 RIOX2 AntibodyA32122-2
TargetRIOX2
  • SizePrice
Western blot analysis of MINA in human heart tissue lysate with MINA antibody at (A) 1 and (B) 2 microg/mL.
Product group Antibodies
Boster Bio
Anti-MINA RIOX2 AntibodyA32122
TargetRIOX2
  • SizePrice
Figure 1. Western blot analysis of RETREG1 using anti-RETREG1 antibody (A32125). 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 U-87MG whole cell lysates, Lane 2: 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-RETREG1 antigen affinity purified polyclonal antibody (Catalog # A32125) 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 RETREG1 at approximately 55 kDa. The expected band size for RETREG1 is at 55 kDa.
Product group Antibodies
Boster Bio
Anti-RETREG1 Antibody Picoband(r)A32125-10UG
TargetRETREG1
  • SizePrice
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