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Table 3 Primer sequences and reaction conditions used in nested PCR amplifications

From: Molecular characterization and distribution of Cryptosporidium spp., Giardia duodenalis, and Enterocytozoon bieneusi from yaks in Tibet, China

Locus

Primer sequences (5′-3′)

Nucleotide fragment (bp)

Annealing temperature (°C)

Reference

Cryptosporidium SSU rRNA

SSU-F2: TTCTAGAGCTAATACATGCG

840

55

[57]

SSU-R2:CCCATTTCCTTCGAAACAGGA

SSU-F3:GGAAGGGTTGTATTTATTAGATAAAG

55

SSU-R4:CTCATAAGG TGCTGAAGGAGTA

G. duodenali SSU rRNA

Gia2029: AAGTGTGGTGCAGACGGACTC

292

55

[58]

Gia2150c: CTGCTGCCGTCCTTGGATGT

RH11: CATCCGGTCGATCCTGCC

59

RH4: AGTCGAACCCTGATTCTCCGCCCAGG

G. duodenalis tpi

AL3543: AAATIATGCCTGCTCGTCG

530

50

[59]

AL3546: CAAACCTTITCCGCAAACC

AL3544: CCCTTCATCGGIGGTAACTT

50

AL3545: GTGGCCACCACICCCGTGCC

E. bieneusi ITS

EBITS3: GGTCATAGGGATGAAGAG

389

57

[60]

EBITS4: TTCGAGTTCTTTCGCGCTC

EBITS1: GCTCTGAATATCTATGGCT

55

EBITS2.4: ATCGCCGACGGATCCAAGTG