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Antibody ID methodology


RR1

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More laboratories are using solid phase techniques for antibody screening. When an antibody is detected by a solid phase panel- and specificity cannot be identified, would labs normally refer these to reference labs, and if so..what techniques would the reference labs use to identify the antibody?

My current practice is to perform a second panel by Gel. However the manufacturers claim we may be missing Anti-Jka, anti-Jb antibodies.

What is the 'gold standard' technique for antibody identification ?

Thanks!

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As a Reference Laboratory (actually, your Reference Laboratory, Rashmi) we use the DiaMed gel technique as our first "line of defence", but if we do not detect anything by this technique, we will go on to perform LISS tube IAT at 37oC. We consider this latter technique to be the "gold standard", and if we do not detect anything by this technique, we look no further (on the grounds that, if we don't detect an antibody by this technique, even if there is one present, it is unlkely to be clinically significant.

Just occasionally, we will perform a LISS tube direct agglutination at 15oC, if we think that the referring laboratory may have detected a "cold reacting" antibody with a true specificity, such as anti-M, but only if it's a slow day and we are bored!

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Excellent idea ! ...it would be for a very worthy cause...and help everyone develop a better understanding of the different techniques being used and their limitations/ good points.

When are going to start this?!!

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  • 2 months later...

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