• Keine Ergebnisse gefunden

Table S1. PCR primers, target loci, and thermal cycles used in this study.

N/A
N/A
Protected

Academic year: 2022

Aktie "Table S1. PCR primers, target loci, and thermal cycles used in this study."

Copied!
2
0
0

Wird geladen.... (Jetzt Volltext ansehen)

Volltext

(1)

Table S1. PCR primers, target loci, and thermal cycles used in this study.

Primer Locu s

PCR cycle References

LCO-1490 COI 3 min 95°, 35 cycles of (1 min 95°, 1 min 40°, 1.5 min 72°), 7 min 72° C

Folmer et al. 1994 16Sar-b 16S 3 min 95°, 35 cycles of (30 sec 94°, 30 sec

49°, 1 min 72°), 5 min 72° C Palumbi 1994 Brandner et al. 2017 16Sbr-H 16S 3 min 95°, 35 cycles of (30 sec 94°, 30 sec

49°, 1 min 72°), 5 min 72° C Palumbi 1994 Brandner et al. 2017 ECOIC COI 3 min 95°, 35 cycles of (30 sec 94°, 30 sec

49°, 1 min 72°), 5 min 72° C

Hrincevich and Foltz 1996 Foltz et al. 2007

18S-R 18S 3 min 95°, 35 cycles of (30 sec 94°, 30 sec 49°, 1 min 72°), 5 min 72° C

Hrincevich and Foltz 1996 Foltz et al. 2007

18S-1F 18S 3 min 95°, 35 cycles of (30 sec 94°, 30 sec 49°, 1 min 72°), 5 min 72° C

Fuchs et al. 2009

Table S2. Number of specimens sequenced per morphotype.

Larval morphotype Primer used No. PCRs No. sequences No. matches

Golfingia elongata LCO-1490 2 1 1

16Sar-b 2 1 0

16Sbr-H 2 2 0

Embryo LCO-1490 2 1 0

16Sar-b 1 1 1

16Sbr-H 1 0 0

Nipponemertes pulchra LCO-1490 1 1 0

16Sar-b 1 0 0

16Sbr-H 2 2 0

Bivalve veliger 16Sar-b 2 1 0

16Sbr-H 5 4 0

Nudibranch veliger LCO-1490 1 1 0

16Sbr-H 2 2 0

Alcyonidium sp. LCO-1490 3 1 1

18S-1F 3 3 0

Cerianthus lloydi LCO-1490 1 1 0

ECOIC 1 1 0

18S-R 1 1 0

Asteroid LCO-1490 1 1 0

ECOIC 2 2 0

18S-R 2 2 0

Parenchymella LCO-1490 1 1 0

16Sbr-H 1 1 0

Polychaete1 LCO-1490 3 0 0

Unknown LCO-1490 1 0 0

Total 44 31 3

(2)

References

Brandner MM, Stübner E, Reed AJ, et al. (2017) Seasonality of bivalve larvae within a high Arctic fjord. Polar Biol 40:263–276. https://doi.org/10.1007/s00300-016-1950-x

Folmer O, Black M, Hoeh W, et al. (1994) DNA primers for amplification of mitochondrial cytochrome c oxidase subunit I from diverse metazoan invertebrates. Mol Mar Biol Biotechnol 3:294–299

Foltz DW, Bolton MT, Kelley SP, et al (2007) Combined mitochondrial and nuclear sequences support the monophyly of forcipulatacean sea stars. Mol Phylog 43:627–634.

https://doi.org/10.1016/j.ympev.2006.10.012

Fuchs J, Obst M, Sundberg P (2009) The first comprehensive molecular phylogeny of Bryozoa (Ectoprocta) based on combined analyses of nuclear and mitochondrial genes. Mol

Phylogenet Evol 52:225–233. https://doi.org/10.1016/j.ympev.2009.01.021

Hrincevich AW, Foltz DW (1996) Mitochondrial DNA sequence variation in a sea star (Leptasterias spp.) species complex. Mol Phylogenet Evol 6:408–415

Palumbi SR (1994) Genetic divergence, reproductive isolation, and marine speciation. Annu Rev Ecol Syst 25:547–572

Referenzen

ÄHNLICHE DOKUMENTE

ΔamyR-down-F AACGGTATTGACTAAAAGGGGAAGGCAACTACGACGATGACG ΔamyR-down-R TCGGTACCCGGGGATCCGATATTCATGTCTCCTGCGGAAATGG ΔcpcA-up-F ATCTACTAGTCATATGGATTGGGCCCGGTGATTGGCGGCGAGATCCG

AGGGCACGCACGTTGAG SNP, single-nucleotide polymorphism; PCRP, primer for polymerase chain reaction; UEP_SEQ, primer for single

The two sets of clusters were used to predict binding behaviour of LacI at different pH values (Fig. S34 LacI-DNA binding results of the HADDOCK webserver for pH 7..

aci01347_down_fwd GCATGGATCCGTGACGGCTTTACCATTCATCGTG aci01347_down_rev ATTACTGCAGAAAGTTCATGGCCTCGGTGCGGACATAC aci01347_ctr_fwd ATCCATACGACCCGTAGGCGTACTGAG.

AQP2 Forward GAGATCACGCCAGCAGACAT 59°C Reverse GAAGAGCTCCACAGTCACCG. AQP3 Forward TGCTACCTACCCCTCTGGAC 56°C

Primers designed for usage with a seamless cloning kit (SCK). MssI sites, introduced by respective 5’ FW and 3’ rev primers, were chosen the way that no scar occurs after

[r]

a Primer and probe modifications: Bio Biotin, DIG Digoxin, FITC Fluorescein isothiocyanate isomer, THF Tetrahydrofuran, C3-spacer 3’