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 entomological origin of honey was detected in the subtropical  Apis cerana cerana  using two sets of  Major Royal Jelly Protein 2  ( mrjp2 ) primers. Due to the high genetic divergence of  A. cerana , this study aimed to confirm that the primers can be used to detect honey origin from  A c. javana  and  Apis mellifera  in Indonesia. The  mrjp2  gene was amplified using M-F M-R and C-F C-R primers at various annealing temperatures to find the optimal temperature based on the presence-absence of the amplicon. Honey was successfully differentiated from 11 colonies of  A. mellifera  and  A. c. javana  using M-F and M-R primers at annealing temperatures of 50 °C, 53 °C, 55 °C, 57 °C, and 59 °C. However, caution should be placed on using these primers when used to amplify  A. cerana  at 47 °C. This study confirmed that C-F and C-R primers are specifically applicable when amplifying  A. c. javana .

journal of apicultural research

Entomological origin detection of honey from  Apis mellifera  and  Apis cerana javana  in Indonesia based on the Major Royal Jelly Protein 2 (mrjp2) gene