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Immunohistochemical analysis of paraffin-embedded human tonsil, using CD86 Antibody (M00220-1) CD86 was detected in paraffin-embedded tissue section. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-CD86 Antibody (M00220-1)overnight at 4°C. Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
Product group Antibodies
Boster Bio
Western blot analysis of LRRK2 expression in GFP-LRRK2 lysate.
Product group Antibodies
Boster Bio
Immunohistochemical analysis of paraffin-embedded human thyroid, using LRRK2 Antibody(M00221-2) LRRK2 was detected in paraffin-embedded tissue section. Heat mediated antigen retrieval was performed in citrate buffer (pH6, epitope retrieval solution) for 20 mins. The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1ug/ml rabbit anti-LRRK2 Antibody (M00221-2)overnight at 4 Biotinylated goat anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37 The tissue section was developed using Strepavidin-Biotin-Complex (SABC)(Catalog # SA1022) with DAB as the chromogen.
Product group Antibodies
Boster Bio
Western blot analysis of LRRK2 in HEK293 cell lysate transfected with 3*Flag wild type, full length LRRK2 (M00221). 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. 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-LRRK2 monoclonal antibody (Catalog # M00221) 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 1:10000 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 LRRK2
Product group Antibodies
Boster Bio
Western blot analysis of BRG1 expression in HeLa cell lysate.
Product group Antibodies
Boster Bio
Western blot analysis of TNFAIP3 expression in Jurkat cell treated with TNF + TPA lysate (M00224). 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. 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-TNFAIP3 monoclonal antibody (Catalog # M00224) 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 1:10000 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 TNFAIP3
Product group Antibodies
Boster Bio
Western blot analysis of AhR expression in HEK293 cell lysate.
Product group Antibodies
Boster Bio
Immunohistochemical analysis of paraffin-embedded human bladder cancer, using GAPDH Antibody.
Product group Antibodies
Boster Bio
Immunofluorescent analysis of HeLa cells, using GAPDH Antibody.
Product group Antibodies
Boster Bio
Western blot analysis of Tuberin expression in Jurkat cell lysate.
Product group Antibodies
Boster Bio
Western blot analysis of IL4 expression in human tonsil lysate.
Product group Antibodies
Boster Bio
Western blot analysis of FGFR2 expression in (1) MCF-7 cell lysate; (2) Mouse brain lysate (M00231). 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. 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-FGFR2 monoclonal antibody (Catalog # M00231) 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 1:10000 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 FGFR2
Product group Antibodies
Boster Bio