" and few books seem to provide that information"

Probably because it is so disgusting!

We used to SPIT on the sections to cover, incubate at room temp for 10 min and 
rinse well in water.
If we had too many slides to do (I could probably SPIT on 3 slides before I 
dried up) I would spit into a 50ml specimen container and add PBS buffer, equal 
volumes, mix and pipette on to the slides and incubate for 10-15 min at room 
temp.

Regards 
Tony Henwood JP, MSc, BAppSc, GradDipSysAnalys, CT(ASC), FFSc(RCPA) 
Laboratory Manager & Senior Scientist 
Tel: 612 9845 3306 
Fax: 612 9845 3318 
the children's hospital at westmead
Cnr Hawkesbury Road and Hainsworth Street, Westmead
Locked Bag 4001, Westmead NSW 2145, AUSTRALIA 

-----Original Message-----
From: [email protected] 
[mailto:[email protected]] On Behalf Of Monfils, Paul
Sent: Saturday, 12 February 2011 9:42 AM
To: [email protected]
Subject: [Histonet] saliva for glycogen hydrolysis

Those who use human saliva rather than diastase - for how long do you apply the 
saliva?  At what temperature?  Do you cover the saliva and section with a 
coverslip during treatment?  I used to do this many years ago, but have been 
using diastase for so long now that I don't remember the particulars of the 
saliva method, and few books seem to provide that information.  Thanks.

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