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RBC hemolysis


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#1 ujla80

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Posted 15 December 2009 - 07:53 AM

dear friends :)

i have problem in getting clear serum from mice blood. i collect the blood from orbital sinus (eye), keep it at 37 C for 1 hr. then keep it in fridge (4 degree C) for 3-4 hrs. but when i centrifuge it, blood gets hemolysed. this prob doesn't occur with rabbit blood. whats the reason for the hemolysis, because i handle the sample very gently? please help..
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#2 aimikins

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Posted 15 December 2009 - 04:19 PM

I think this can happen during the eyebleed. you might try for a larger bore capillary tube? sometimes that can help, although you need very precise technique or this is harder on the mice.

I'd also be concerned about the time at 37C; that will only accelerate the hemolysis.

you might try bleeding via saphenous leg vein stick; there seems to be less trauma to the tissue and less hemolysis.

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#3 Doki

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Posted 15 December 2009 - 06:12 PM

why do U have to keep the sample for such a long time before U centrifuge?
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#4 ujla80

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Posted 16 December 2009 - 07:20 AM

one hr incubation at 37 C is recommended before centrifugation. there is no specific reason for  putting clotted blood samples in fridge.i do it because i dont have to collect serum immediately.  




View PostNabi, on Dec 15 2009, 06:12 PM, said:

why do U have to keep the sample for such a long time before U centrifuge?

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#5 sgt4boston

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Posted 18 December 2009 - 12:19 PM

Why can't you use a serum separation tube?

#6 Gerard

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Posted 18 December 2009 - 01:40 PM

First, did you check the hemolysis is not present in vivo?
Otherwise there is the possibility the celmembrane is very fragile by nature and then you can try to use less G's by centrifugation.
Ockham's razor
          Pluralitas non est ponenda sine necessitate
-- "You must assume no plural without necessity".

#7 ujla80

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Posted 18 December 2009 - 06:02 PM

no..how can i check it?


View PostGerard, on Dec 18 2009, 01:40 PM, said:

First, did you check the hemolysis is not present in vivo?
Otherwise there is the possibility the celmembrane is very fragile by nature and then you can try to use less G's by centrifugation.

god is great

#8 Gerard

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Posted 19 December 2009 - 04:25 AM

After clotting you should see bloodserum that is the yellow liquid apart from the clot, when there is strong hemolysis there is almost no difference in color between serum and clot.
Ockham's razor
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-- "You must assume no plural without necessity".

#9 aimikins

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Posted 20 December 2009 - 03:07 PM

sgt., the serum-separator tubes are often not very effective with really small volumes of blood, like when you want to do serial bleeds on the same mouse.
"it is a miracle that curiosity survives formal education" -A.E.

#10 bachai

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Posted 22 December 2009 - 06:47 PM

I often had hemolysis on eye bleeding. And the worst was I made a number of poor creatures blind after serial bleeds.
Then I had much less hemolysis and spent less time with tail bleeding. Prewarm mice 3-5min before bleeding. No anaesthesia required by my institution animal ethics. Use a mouse strainer to fix the animal except the tail. I got ~50uL serum per mouse this way every fortnight. Of course you could get more but the animal ethics may not allow you to. In general I believe tail bleeding is less stressful both for me and mice.

#11 ujla80

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Posted 23 December 2009 - 06:19 PM

thats right bachai, i have tried tail bleed but could not get blood..i need at least 200microL blood.





View Postbachai, on Dec 22 2009, 06:47 PM, said:

I often had hemolysis on eye bleeding. And the worst was I made a number of poor creatures blind after serial bleeds.
Then I had much less hemolysis and spent less time with tail bleeding. Prewarm mice 3-5min before bleeding. No anaesthesia required by my institution animal ethics. Use a mouse strainer to fix the animal except the tail. I got ~50uL serum per mouse this way every fortnight. Of course you could get more but the animal ethics may not allow you to. In general I believe tail bleeding is less stressful both for me and mice.

god is great




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