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. 2009 Dec 9;15:2649–2662.

Table 1. PCR Primers.

Entrez Gene ID Gene Primers (5′-3′)
2044
Eph-A5
F: ACCGATGAACCTCCCAAAAT
R: TAGCCTGCTGCTGTACGTG
285220
Eph-A6
F: TGGGATGCCATCACTGAAAT
R: CAAGAGGAACCAGCCAATCT
2045
Eph-A7
F: GATCCCAGAGGCTCTTTGC
R: TTGATGGACAGCTCTATTTGG
2047
Eph-B1
F: AGCTGCTCCCGCTGTGAC
R: TGCTCCGATGACCTCTTCA
1942
ephrin-A1
F: TCCGGAATGAGGACTACACC
R: AGTGCCTGTCCCTCTCTTCA
1943
ephrin-A2
F: GCTGCTGCTCCTGCTGTTAC
R: CTCGCCGTTGACCATGTA
1944
ephrin-A3
F: CCTGCACTGGAAGTGTCTGA
R: ACCAGGAGTCAGGGAAAGGT
1945
ephrin-A4
F: TGGAGAGAGTGGCACATCAG
R: GGAGGGCAACAAAAAGATGA
1946
ephrin-A5
F: GATGTGTGTGTTCAGCCAGG
R: AGGGAGGCAGGAACAAGTTT
1948 ephrin-B2 F: TAACCAGGAGGGAGGGGTGT
R: GCCGAATGCTACAAGACTAGG

PCR of several A-class Ephs and ephrins as well as Eph-B1 and ephrin-B2 was run using cDNA from four fetal human retinas of 17–20 WG. The PCR products for Eph-A5, -A6, -A7, -B1 and ephrin-A1, -A4, and -B2 were then used to generate DIG-labeled riboprobes for in situ hybridization.