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The scaffolds were observed under a fluorescence
stereomicroscope (Leica MZ FL b, Leica Microsystems,
Glattbrugg, Switzerland) to assess the regional distribution
of the living cells in green (calcein staining) (¼¤·¢²¨³¤480/40
nm, ·¢É䲨³¤ 510 nm) and dead cells in red (PI staining)
(¼¤·¢²¨³¤ 546/10 nm, ·¢É䲨³¤590 nm).


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shileinjut(½ð±Ò+1): лл²ÎÓ룡 2011-02-05 17:26:14
ÒýÓûØÌû:
Originally posted by dj04164 at 2011-02-01 10:11:49:
480nmÊÇÓ«¹âÏÔ΢¾µÅäµÄÂ˲¨Æ¬µÄ¼¤·¢²¨³¤£¬ºóÃæµÄ40ÊÇ-/+ 20nm¡£ºóÃæµÄ546/10Ò»Ñù

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americanyk(½ð±Ò+3): ÐÂÄê¿ìÀÖ 2011-02-02 16:49:36
Calcein AM reacts with intracellular esterase to produce green fluorescence at 490nm while PI enters only dead cells with damaged membranes which produce red fluorescence at 545nm upon binding to nucleic acids
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2Â¥2011-02-01 09:45:48
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dj04164

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americanyk(½ð±Ò+2): ÐÂÄê¿ìÀÖ 2011-02-02 16:49:51
480nmÊÇÓ«¹âÏÔ΢¾µÅäµÄÂ˲¨Æ¬µÄ¼¤·¢²¨³¤£¬ºóÃæµÄ40ÊÇ-/+ 20nm¡£ºóÃæµÄ546/10Ò»Ñù
3Â¥2011-02-01 10:11:49
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joymyself2006

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ÒýÓûØÌû:
Originally posted by dj04164 at 2011-02-01 10:11:49:
480nmÊÇÓ«¹âÏÔ΢¾µÅäµÄÂ˲¨Æ¬µÄ¼¤·¢²¨³¤£¬ºóÃæµÄ40ÊÇ-/+ 20nm¡£ºóÃæµÄ546/10Ò»Ñù

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