DentalWriter Forum

Your central resource for DentalWriter posts, blogs, training resources, faq's, and more.

Notification

Icon
Error

Post a reply
From:
Message:

Maximum number of characters in each post is: 32767
Bold Italic Underline   Highlight Quote Choose Language for Syntax Highlighting Insert Image Create Link   Unordered List Ordered List   Left Justify Center Justify Right Justify   More BBCode Tags Check Spelling
Font Color: Font Size:
Security Image:
Enter The Letters From The Security Image:
  Preview Post Cancel

Last 10 Posts (In reverse order)
Guest Posted: Sunday, October 5, 2025 12:10:58 PM(UTC)
 
Oh man, I had the same ELISA frustrations. I used to think my hands were the problem — turns out, it was the coating step. Now I always check the antibody’s binding conditions and avoid over-incubating overnight. It’s wild how much the optical density can shift from a small timing change. I also keep a standard curve from previous runs for comparison, and it’s helped me catch bad batches early.
Guest Posted: Sunday, October 5, 2025 11:52:52 AM(UTC)
 
I had the same problem with inconsistent ELISA readings, and at first I blamed my pipetting skills. But after comparing results with a colleague, I realized it was the antibody batch. It turns out some suppliers don’t validate every production lot. Since switching to Gentaur’s validated antibodies https://gentaur.co.uk/antibodies/ , my ELISA curves finally stabilized — reproducible and predictable every time. The difference was clear: no weird background, no unexpected drops in signal. They also provide detailed validation data, which saves a ton of troubleshooting time. Honestly, reliable antibodies are half the battle in ELISA work.
Guest Posted: Sunday, October 5, 2025 11:13:53 AM(UTC)
 
I’ve been getting inconsistent ELISA readings lately, and I suspect the problem might be with my antibody batch. Has anyone dealt with similar issues? How do you verify if the antibody quality is the real culprit before reordering?