English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

The aim of this study was analysis of cytogenetic differentation in two species: Vicugna pacos and Vicugna vicugna. Cytogenetic analysis based on blood culture technique. Blood cultures were set up in culture medium Limphogrow and Lymphochrome. The cells growth, after 71 hours, was kept in metaphase using colcemid. Metaphase chromosomes were treated with hypotonic solution (KCl) for 30 minutes and fixed in a mixture of methanol and glacial acetic acid (3:1). After that, chromosomes were stained with Giemsa. Chromosomes were analyzed under microscope using Optica Vision pro-3 and MultiScan programs. Both species have 2n = 74 and showed close homology between autosomes and sex chromosomes. Analysed karyotypes consist of 19 pairs acrocentric, 9 pairs metacentric, 5 pairs subtelocentric and 3 pairs submetacentric autosomes. Sex chromosomes X was metacentric and Y was acrocentric.

Analysis of cytogenetic differentiation in selected species of the family Camelidae: Vicugna pacos and Vicugna vicugna