Agrisera is a Swedish company offering the most well-published plant antibodies, combined with high titer secondary antibodies, blocking and detection reagents. Over 40 years in the antibody business have taught us a lot, and we are proud to say there are few problems we cannot help you solve. Our experienced scientific staff are on hand to answer all your antibody queries promptly.

Est. 1985

Choosing the right antibodies for your research, voiceover
3:32
Choosing the right antibodies for your research, voiceover
Choosing the right antibodies for your research
3:06
Choosing the right antibodies for your research
Agrisera Western blot workshop, United Kingdom, held 2024-12-10
1:12:21
Agrisera Western blot workshop, United Kingdom, held 2024-12-10
Agrisera Western blot workshop, Taiwan 2024, part 2
1:02:46
Agrisera Western blot workshop, Taiwan 2024, part 2
Agrisera Western blot workshop, Taiwan 2024, part 1
1:01:59
Agrisera Western blot workshop, Taiwan 2024, part 1
Agrisera Western blot workshop, Australia/New Zealand, held 2024-03-20
1:33:57
Agrisera Western blot workshop, Australia/New Zealand, held 2024-03-20
How do I cite antibodies in scientific papers?
1:01
How do I cite antibodies in scientific papers?
Can I use the same antibody in different species and applications?
2:02
Can I use the same antibody in different species and applications?
What Western blot protocol should I use?
2:42
What Western blot protocol should I use?
How to get an intense signal in Western blot using a weak antibody?
1:57
How to get an intense signal in Western blot using a weak antibody?
Why isn't my epitope tag antibody working?
2:14
Why isn't my epitope tag antibody working?
How do I determining the molecular weight of my target protein?
1:44
How do I determining the molecular weight of my target protein?
Which detection method should I use?
0:38
Which detection method should I use?
When should I use colorimetric detection?
1:06
When should I use colorimetric detection?
When should I use fluorescent detection?
1:30
When should I use fluorescent detection?
When should I use chemiluminescent detection?
3:40
When should I use chemiluminescent detection?
What are the key considerations for selecting secondary antibodies?
3:33
What are the key considerations for selecting secondary antibodies?
Which antibody incubation buffer should I use?
3:17
Which antibody incubation buffer should I use?
How do I know that I have equal protein load per well?
1:48
How do I know that I have equal protein load per well?
How do I perform antibody titration for optimal results?
1:00
How do I perform antibody titration for optimal results?
How is membrane blocking done?
4:05
How is membrane blocking done?
How do I remove background in Western blot?
2:21
How do I remove background in Western blot?
Primary antibody does not work – What to do?
2:04
Primary antibody does not work – What to do?
Can primary antibodies be reused?
1:37
Can primary antibodies be reused?
Which antibody format is better – serum, total IgG or affinity purified?
2:48
Which antibody format is better – serum, total IgG or affinity purified?
How do I know if the protein transfer was successful?
3:16
How do I know if the protein transfer was successful?
How do I remove air bubbles when assembling a Western blot sandwich?
1:22
How do I remove air bubbles when assembling a Western blot sandwich?
How do I succeed with gel electrophoresis?
5:58
How do I succeed with gel electrophoresis?
Is wet or semi-dry protein transfer more efficient?
1:08
Is wet or semi-dry protein transfer more efficient?
Which membrane is better – PVDF or Nitrocellulose?
1:36
Which membrane is better – PVDF or Nitrocellulose?