Table 1 Description of PCR primers.

From: Analysis of the impact of DGAT1 p.M435L and p.K232A variants on pre-mRNA splicing in a full-length gene assay

Name

Sens

Sequence

Use

C1

F

TACCGAGCTCGGATCCACACAGACAAGGACGGAGAC

DGAT1 cloning

C2

R

GCCCTCTAGACTCGAGCAAAGCAGTCCAACACCCACG

DGAT1 cloning

M1

F

GGCCTTCACCGGCCTGATGGCGCAGGTGA

p.M435L mutagenesis

M2

R

TCACCTGCGCCATCAGGCGGTGAAGGCC

p.M435L mutagenesis

M3

F

GTAGCTTTGGCAGGTAAGGCGGCCAACGGGGGAGCTG

p.K232A mutagenesis

M4

R

CAGCTCCCCCGTTGGCCGCCTTACCTGCCAAAGCTAC

p.K232A mutagenesis

P1

F

ACACAGACAAGGACGGAGAC

Qualitative DGAT1 RT-PCR

P2

R

GTAGTTGCCGCGGAAGAAG

Qualitative DGAT1 RT-PCR

P3

F

TCAAGCTGTTCTCCTACCGG

Qualitative DGAT1 RT-PCR

P4

R

GGGGCGAAGAGGAAGTAGTA

Qualitative DGAT1 RT-PCR

P5

F

CAAGTGGGCAGCCAGGAC

Qualitative DGAT1 RT-PCR

P6

F

CTGGCTAGCGTTTAAACTTAAGC

Qualitative pcDNA3.1 UTR RT-PCR

P7

R

GATCAGCGGGTTTAAACGGG

Qualitative pcDNA3.1 UTR RT-PCR

Q1

F

ACACAGACAAGGACGGAGAC

Quantitative DGAT1 RT-PCR

Q2

R

GGGTCAAAGGTTAGGGGTCA

Quantitative DGAT1 RT-PCR

Q3

R

TGAAGCCACTGTCAGAACTG

Quantitative DGAT1 RT-PCR

Q4

F

AACTACCGTGGCATCCTGAA

Quantitative DGAT1 RT-PCR

Q5

R

ACCGTGCGTTGCTTAAGAT

Quantitative DGAT1 RT-PCR

Q6

R

ACAGAGCTCCATTCACCACA

Quantitative DGAT1 RT-PCR

Q7

F

TCAAGCTGTTCTCCTACCGG

Quantitative DGAT1 RT-PCR

Q8

R

CGAGGCAGCCCTCACCAG

Quantitative DGAT1 RT-PCR

Q9

R

CTTACCTGCCAAAGCAGC

Quantitative DGAT1 RT-PCR

Q10

F

ACGTGGATCCTGAGAACTTCA

Quantitative pcAT7-Glo1 RT-PCR

Q11

R

TAAACGGGCCCTCTAGAGC

Quantitative pcAT7-Glo1 RT-PCR

  1. See Figs. 1A, 2A, 5B for details about “P” and “Q” primer pairs usage.