8 Questions 10 Answers 0 Followers
Questions related from Zahran Somaya
I'm working on detecting different fragments of cardiac Troponin I (Not using a kit) in the patients' sera of different cardiac diseases. I'm using the best antibodies recommended by Hytest (19c7...
03 March 2016 3,046 3 View
Just wondering how I can stick the 2 antibodies to the wall of the plate? as I have them in separate aliquots. Should I incubate the first Ab O/N then next day incubate the other for another...
09 September 2015 7,139 3 View
I'm detecting Troponin I, using 19C7 for capturing, and M19 for detection. 1% BSA for blocking. I get signals with the troponin compared to the negative control, but it doesen't correlate with the...
04 April 2015 4,539 7 View
I'm using 19C7 2ug/mL as capture, and M18 1 ug/mL as detection for Troponin I in ELISA, with SA-HRP. somedays, I get reliable results, and many others, it's all over the place :(( when...
04 April 2015 676 4 View
I work on Troponin I, I use 19C7 as a capture, and M18 for detection both at 1ug/mL, I need the assay to detect down to 0.1 ng/mL, and I'm just getting signal at 50 ng/mL. I use 2% BSA for block....
04 April 2015 9,533 3 View
I need help with making precoated ELISA plates, especially preserving. I never did this before, but it will save me a lot of time. What I found with google search is: incubate with capture...
04 April 2015 5,592 6 View
I cleave my protein from its vector using Ni sulfate under high temperature and PH, after lyophilizing. My protein came out yellowish, and it should be white, so I assumed that there are some...
12 December 2014 4,305 5 View
I have a problem with my protein purification, I'm using the Ni column chromatography, running my cTnI protein after cleavage from the His tag to get the protein without the His tag, but it's...
11 November 2014 8,342 7 View