Pollen dynamics: Difference between revisions

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[[Image:Fruiting.png|thumb|200px|right| Fruiting Status - Mulugu - Dec2008]]
[[Category:Projects]]
* Resources:
[[Category:Pollen_dynamics]]
:[http://www.download.rajkumar.in/itc/readings/pollen/Pollen_flow_grandis_peternity.pdf Pollen flow in Eucalyptus grandis determined by paternity analysis using microsatellite markers]
: Tree Genetics & Genomes (2008) 4:37–47
* [[Vishwanath]]
** Title: Pollen flow in Eucalyptus seed orchards as determined by paternity analysis
* [[Gene_Flow_Progress]]
----
* Work plan: [[Pollen_Dynamics]]
* Logistics
** 15 Maternal/Paternal* 25 progenies = 375 plants to be analyzed
** DNA Isolation: 375 samples
** PCR reaction : 375 * 20 = 7500
** Gel Run: 7500/60 = 125 runs in acrylamide (30+30 samples)
----
* Requirements
** Trays
** Qiagen DNA isolation kit: 2 (each can handle 250 samples)
** Ampli Taq 2 vials
** High resolution Agarose: 100g
----
* Strategy
** Seeds sowing
** Leaf sample collection from parental trees (15) and seedlings after one and half month
** DNA isolation from 375 samples
** Take representative sample and screen the primers to select 20 good
** PCR with 375 x 20 SSR primers
** Score them and make an automated DB for analysis
** Make meaningful predictions for the Mulugu SSO
----
[[Category:Readings]] [[Category:Rajkumar]] [[Category:Silvi]]

Latest revision as of 17:24, 14 February 2017

Fruiting Status - Mulugu - Dec2008
  • Resources:
Pollen flow in Eucalyptus grandis determined by paternity analysis using microsatellite markers
Tree Genetics & Genomes (2008) 4:37–47

  • Work plan: Pollen_Dynamics
  • Logistics
    • 15 Maternal/Paternal* 25 progenies = 375 plants to be analyzed
    • DNA Isolation: 375 samples
    • PCR reaction : 375 * 20 = 7500
    • Gel Run: 7500/60 = 125 runs in acrylamide (30+30 samples)

  • Requirements
    • Trays
    • Qiagen DNA isolation kit: 2 (each can handle 250 samples)
    • Ampli Taq 2 vials
    • High resolution Agarose: 100g

  • Strategy
    • Seeds sowing
    • Leaf sample collection from parental trees (15) and seedlings after one and half month
    • DNA isolation from 375 samples
    • Take representative sample and screen the primers to select 20 good
    • PCR with 375 x 20 SSR primers
    • Score them and make an automated DB for analysis
    • Make meaningful predictions for the Mulugu SSO