Skip to main content
. 2018 May 16;293(25):9555–9569. doi: 10.1074/jbc.RA118.002836

Table 1.

Primers used in the study

Shown are sequences of primers used to generate CRT-null lines (KO CRT), the CRT-FS mutants with the KDEL sequence, and the CRT-WT lacking the KDEL sequence (cloning) and used in qPCR analysis.

Primer no. Primer name Sequence (5′ to 3′) Purpose
1 CRTgRNA-1f GCCTGCCGTCTACTTCA KO CRT
2 CRTgRNA-2r TTTGGATTCGATCCAGC KO CRT
3 CRT-Fwd CTAGCTAGTTAATTAAGGATCCATGCTGCTATCCGTGCCGC Cloning
4 CRT-FS + KDELr CTCGAGGCCTGCAGGAATTCCTACAGCTCGTCCTTGGCCTCAGTCCAGCCC Cloning
5 CRT-WT-KDELr CTCGAGGCCTGCAGGAATTCCTAGGCCTGGCCGGGGAC Cloning
6 CRT-RTf GAATACAACATCTGGTTTGGTCCCGAC qPCR
7 CRT-RTr CAATCAGTGTGTACAGGTGTGTAAAC qPCR
8 LMP1-RTf ACAAAACTGGTGGACTC qPCR
9 LMP1-RTr GTCTGCCCTCGTTGGA qPCR
10 β-Actin-RTf GGCATCGTGATGGACTCCG qPCR
11 β-Actin-RTr GCTGGAAGGTGGACAGCGA qPCR