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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.

If you need a specific antibody and can’t find it in our webshop, please contact our technical support.

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Figure 1. Western blot analysis of ODAPH using anti-ODAPH antibody (A32235-1). 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 placenta tissue 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-ODAPH antigen affinity purified polyclonal antibody (Catalog # A32235-1) 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 ODAPH at approximately 20 kDa. The expected band size for ODAPH is at 16 kDa.
Product group Antibodies
Boster Bio
Anti-ODAPH Antibody Picoband(r)A32235-1-CY3
TargetODAPH
  • SizePrice
Figure 1. Western blot analysis of ODAPH using anti-ODAPH antibody (A32235-1). 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 placenta tissue 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-ODAPH antigen affinity purified polyclonal antibody (Catalog # A32235-1) 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 ODAPH at approximately 20 kDa. The expected band size for ODAPH is at 16 kDa.
Product group Antibodies
Boster Bio
Anti-ODAPH Antibody Picoband(r)A32235-1-DYLIGHT488
TargetODAPH
  • SizePrice
Figure 1. Western blot analysis of ODAPH using anti-ODAPH antibody (A32235-1). 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 placenta tissue 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-ODAPH antigen affinity purified polyclonal antibody (Catalog # A32235-1) 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 ODAPH at approximately 20 kDa. The expected band size for ODAPH is at 16 kDa.
Product group Antibodies
Boster Bio
Anti-ODAPH Antibody Picoband(r)A32235-1-DYLIGHT550
TargetODAPH
  • SizePrice
Figure 1. Western blot analysis of ODAPH using anti-ODAPH antibody (A32235-1). 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 placenta tissue 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-ODAPH antigen affinity purified polyclonal antibody (Catalog # A32235-1) 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 ODAPH at approximately 20 kDa. The expected band size for ODAPH is at 16 kDa.
Product group Antibodies
Boster Bio
Anti-ODAPH Antibody Picoband(r)A32235-1-DYLIGHT594
TargetODAPH
  • SizePrice
Figure 1. Western blot analysis of ODAPH using anti-ODAPH antibody (A32235-1). 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 placenta tissue 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-ODAPH antigen affinity purified polyclonal antibody (Catalog # A32235-1) 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 ODAPH at approximately 20 kDa. The expected band size for ODAPH is at 16 kDa.
Product group Antibodies
Boster Bio
Anti-ODAPH Antibody Picoband(r)A32235-1-FITC
TargetODAPH
  • SizePrice
Figure 1. Western blot analysis of ODAPH using anti-ODAPH antibody (A32235-1). 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 placenta tissue 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-ODAPH antigen affinity purified polyclonal antibody (Catalog # A32235-1) 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 ODAPH at approximately 20 kDa. The expected band size for ODAPH is at 16 kDa.
Product group Antibodies
Boster Bio
Anti-ODAPH Antibody Picoband(r)A32235-1-HRP
TargetODAPH
  • SizePrice
Figure 1. Western blot analysis of ODAPH using anti-ODAPH antibody (A32235-1). 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 placenta tissue 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-ODAPH antigen affinity purified polyclonal antibody (Catalog # A32235-1) 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 ODAPH at approximately 20 kDa. The expected band size for ODAPH is at 16 kDa.
Product group Antibodies
Boster Bio
Anti-ODAPH Antibody Picoband(r)A32235-1-IFLUOR647
TargetODAPH
  • SizePrice
Figure 1. Western blot analysis of ODAPH using anti-ODAPH antibody (A32235-1). 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 placenta tissue 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-ODAPH antigen affinity purified polyclonal antibody (Catalog # A32235-1) 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 ODAPH at approximately 20 kDa. The expected band size for ODAPH is at 16 kDa.
Product group Antibodies
Boster Bio
Anti-ODAPH Antibody Picoband(r)A32235-1-PE
TargetODAPH
  • SizePrice
Figure 1. Western blot analysis of ODAPH using anti-ODAPH antibody (A32235-1). 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 placenta tissue 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-ODAPH antigen affinity purified polyclonal antibody (Catalog # A32235-1) 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 ODAPH at approximately 20 kDa. The expected band size for ODAPH is at 16 kDa.
Product group Antibodies
Boster Bio
Anti-ODAPH Antibody Picoband(r)A32235-1
TargetODAPH
  • SizePrice
Western blot analysis of PRKCDBP in A20 cell lysate with PRKCDBP antibody at 1 microg/mL in (A) the absence and (B) the presence of blocking peptide.
Product group Antibodies
Boster Bio
Anti-PRKCDBP CAVIN3 AntibodyA32244
TargetCAVIN3
  • SizePrice
Figure 1. Immunofluorescent staining data of BUD23 using Anti-WBSCR22 BUD23 Antibody (A32249). Immunofluorescence analysis of MCF7 cell using WBSCR22 antibody. Blue: DAPI for nuclear staining.
Product group Antibodies
Boster Bio
Anti-WBSCR22 BUD23 AntibodyA32249
TargetBUD23
  • SizePrice
Figure 1. Western blot analysis of Adam28 using anti-Adam28 antibody (A06873-2). 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 50ug of sample under reducing conditions. Lane 1: rat brain tissue lysates. After Electrophoresis, proteins were transferred to a Nitrocellulose membrane at 150mA 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-Adam28 antigen affinity purified polyclonal antibody (Catalog # A06873-2) 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 Adam28 at approximately 87KD. The expected band size for Adam28 is at 87KD.
Product group Antibodies
Boster Bio
Anti-Adam28 Antibody Picoband(r)A06873-2-DYLIGHT550
TargetAdam28
  • SizePrice
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