Protocol 48859: Sanger sequencing Assay - Msln<em#Strom>-SEQ
Version 1.0

Notes

Mut = ---------------------- (23 bp del)

WT= cacaggcctctttcttggcctca

The genotyping protocol(s) presented here have been optimized for reagents and conditions used by The Jackson Laboratory (JAX). To genotype animals, JAX recommends researchers validate the assay independently upon receipt of animals into their facility. Reaction cycling temperature and times may require additional optimization based on the specific genotyping reagents used.

Expected Results

Sequence

SEQ (deletions in lower case):

CCCTGTCCCCAGTCTCCCcacaggcctctttcttggcctcaCATGTGAGGAGGTAT

Sequence notes have all bp changes noted within plus or minus 30 bp of mutation of interest.  Mutation of interest in bold and red. “Nucleotide changes in bold and red are mutations of interest.  Other bp changes (plus or minus X) are silent mutations.”

JAX Protocol

Protocol Primers

Primer 5' Label Sequence 5' → 3' 3' Label Primer Type Reaction Note
74253 CCC TCA GGT TGT CAC TTG TC Forward A Msln/chr17
74254 TGT ATC TCC CTC AAA CCA TCA TAG T Reverse A Msln/chr17

Reaction A

Component Final Concentration
ddH2O
Kapa 2G HS buffer 1.30 X
MgCl2 2.60 mM
dNTPS-kapa 0.26 mM
74253 0.50 uM
74254 0.50 uM
Glycerol 6.50 %
Kapa 2G HS taq polym 0.03 U/ul
DNA

Cycling

Step Temp °C Time Note
1 94.0 --
2 94.0 --
3 65.0 -- -0.5 C per cycle decrease
4 68.0 --
5 -- repeat steps 2-4 for 10 cycles (Touchdown)
6 94.0 --
7 60.0 --
8 72.0 --
9 -- repeat steps 6-8 for 28 cycles
10 72.0 --
11 10.0 -- hold
JAX uses a very high speed Taq (~1000 bp/sec), use cycling times recommended for your reagents.
JAX uses a 'touchdown' cycling protocol and therefore has not calculated the optimal annealing temperature for each set of primers.

Strains Using This Protocol

Stock Number Strain Name
039444 B6(Cg)-Tracem2(Tcrb,Tcra)Strom Mslnem2Strom/J
039279 C57BL/6J-Tracem1(Tcrb,Tcra)Strom Mslnem1Strom/J
2 strains use this protocol