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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 PRAM1 using anti-PRAM1 antibody (A10037-2). 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 THP-1 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-PRAM1 antigen affinity purified polyclonal antibody (Catalog # A10037-2) 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 PRAM1 at approximately 90 kDa. The expected band size for PRAM1 is at 70,74,90-100 kDa.
Product group Antibodies
Boster Bio
Anti-PRAM1 Antibody Picoband(r)A10037-2-BIOTIN
TargetPRAM1
  • SizePrice
Figure 1. Western blot analysis of PRAM1 using anti-PRAM1 antibody (A10037-2). 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 THP-1 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-PRAM1 antigen affinity purified polyclonal antibody (Catalog # A10037-2) 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 PRAM1 at approximately 90 kDa. The expected band size for PRAM1 is at 70,74,90-100 kDa.
Product group Antibodies
Boster Bio
Anti-PRAM1 Antibody Picoband(r)A10037-2-CY3
TargetPRAM1
  • SizePrice
Figure 1. Western blot analysis of PRAM1 using anti-PRAM1 antibody (A10037-2). 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 THP-1 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-PRAM1 antigen affinity purified polyclonal antibody (Catalog # A10037-2) 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 PRAM1 at approximately 90 kDa. The expected band size for PRAM1 is at 70,74,90-100 kDa.
Product group Antibodies
Boster Bio
Anti-PRAM1 Antibody Picoband(r)A10037-2-DYLIGHT488
TargetPRAM1
  • SizePrice
Figure 1. Western blot analysis of PRAM1 using anti-PRAM1 antibody (A10037-2). 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 THP-1 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-PRAM1 antigen affinity purified polyclonal antibody (Catalog # A10037-2) 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 PRAM1 at approximately 90 kDa. The expected band size for PRAM1 is at 70,74,90-100 kDa.
Product group Antibodies
Boster Bio
Anti-PRAM1 Antibody Picoband(r)A10037-2-DYLIGHT594
TargetPRAM1
  • SizePrice
Figure 1. Western blot analysis of PRAM1 using anti-PRAM1 antibody (A10037-2). 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 THP-1 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-PRAM1 antigen affinity purified polyclonal antibody (Catalog # A10037-2) 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 PRAM1 at approximately 90 kDa. The expected band size for PRAM1 is at 70,74,90-100 kDa.
Product group Antibodies
Boster Bio
Anti-PRAM1 Antibody Picoband(r)A10037-2-IFLUOR647
TargetPRAM1
  • SizePrice
Figure 2. Immunohistochemistry validation of TUBGCP5 using Anti-GCP5 TUBGCP5 Antibody (A10040-2). Immunohistochemical analysis of paraffin-embedded Human brain. Antibody was diluted at 1:100 (4°C
Product group Antibodies
Boster Bio
Anti-GCP5 TUBGCP5 AntibodyA10040-2
TargetTUBGCP5
  • SizePrice
Product group Antibodies
Boster Bio
Anti-RPAB2 POLR2F AntibodyA10044-1
TargetPOLR2F
  • SizePrice
Product group Antibodies
Boster Bio
Anti-POLR2F AntibodyA10044
TargetPOLR2F
  • SizePrice
Western blot analysis of neurotrypsin in 3T3 cell lysate with neurotrypsin antibody at (A) 0.25 and (B) 0.5 microg/mL.
Product group Antibodies
Boster Bio
Anti-Neurotrypsin PRSS12 AntibodyA10045
TargetPRSS12
  • SizePrice
Western blot analysis of extracts from HT-29 cells, using USP42 antibody A10046.
Product group Antibodies
Boster Bio
Anti-USP42 AntibodyA10046
TargetUSP42
  • SizePrice
Product group Antibodies
Boster Bio
Anti-ZNRF1 AntibodyA10050
TargetZNRF1
  • SizePrice
Figure 1. Western blotting validation for Anti-DNAJB9 Antibody A10053 Western blot analysis of extracts of various cell lines
Product group Antibodies
Boster Bio
Anti-DNAJB9 AntibodyA10053
TargetDNAJB9
  • SizePrice
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