Difference between revisions of "Serine Racemase"

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(SR in situ probe)
 
Line 13: Line 13:
  
 
PCR amplification conditions (from Yoshikawa et al, PMID 15337321):  
 
PCR amplification conditions (from Yoshikawa et al, PMID 15337321):  
10-min predenaturation at 95 °C
+
*10-min predenaturation at 95 °C
15-s denaturation at 95  °C.
+
*15-s denaturation at 95  °C.
20-s at 58 °C for serine racemase
+
*20-s at 58 °C for serine racemase
followed by a 20-s extension at 72  °C.
+
*followed by a 20-s extension at 72  °C.

Revision as of 12:35, 12 December 2006

Serine Racemase Probe for in situ hybridization

Primer sequences taken from Yoshikawa et al., PMID 16973158

Rat serine racemase. Genbank Ascension # NM_198757

PCR product Length: 295 bases (+22 bases for T7 promoter] Forward Primer 664 to 683 ATT GCA AGA AAC TGG CCA TC

Reverse Primer [with T7 promoter] 958 to 939 [CTT AAT ACG ACT CAC TAT AGG G] TC AGC AGC GTA CAC CTT CAC

PCR amplification conditions (from Yoshikawa et al, PMID 15337321): *10-min predenaturation at 95 °C *15-s denaturation at 95 °C. *20-s at 58 °C for serine racemase *followed by a 20-s extension at 72 °C.