|
|
Overview
| Library Name | Developing fruit albedo at 80 DAFB in pTriplEx2 vector |
|---|
| Unique Name | Developing fruit albedo at 80 DAFB in pTriplEx2 vector |
|---|
| Organism | Citrus sinensis (Sweet orange) |
|---|
| Type | cdna_library |
|---|
Organ: Fruit; Vector: pTriplEx2; Site_1: SfiIA; Site_2: SfiIB; Developing citrus fruits were harvested from trees growing in the Citrus variety collection in the Wolfskill experimental orchard located in Winters, California (USA). Fruit was collected on July 29, 2003, between 8 to 9 am and stored at 4C. The albedo tissue was dissected out of developing fruit (80 DAFB) and used to isolate RNA using Trizol reagent from Invitrogen. The cDNA Library was constructed using the SMART cDNA library Kit (Clontech). The primary library was en masse evicted and plasmid DNA containing the cDNA library was isolated from the resultant bacterial population. Plasmid DNA was then transformed into ultra competent E coli cells (XL10 Gold; Stratagene). Transformants were plated out on Q-trays (2000 cfu/tray), picked using a Qbot and archived in 384 well dishes.
SNP Chip Base
| Array Name | Developing fruit albedo at 80 DAFB in pTriplEx2 vector |
|---|
| Organism | Citrus sinensis (Sweet orange) |
|---|
| Type | cdna_library |
|---|
Features
The following browser provides a quick view for new visitors. Use the searching mechanism to find specific features.
Pages
Properties
| Property Name | Value |
|---|
| Genbank library cultivar | Washington navel orange |
| Genbank library dev stage | Developing fruit albedo-collected July 29, 2003 |
| Genbank library note | Organ: Fruit; Vector: pTriplEx2; Site_1: SfiIA; Site_2: SfiIB; Developing citrus fruits were harvested from trees growing in the Citrus variety collection in the Wolfskill experimental orchard located in Winters, California (USA). Fruit was collected on July 29, 2003, between 8 to 9 am and stored at 4C. The albedo tissue was dissected out of developing fruit (80 DAFB) and used to isolate RNA using Trizol reagent from Invitrogen. The cDNA Library was constructed using the SMART cDNA library Kit (Clontech). The primary library was en masse evicted and plasmid DNA containing the cDNA library was isolated from the resultant bacterial population. Plasmid DNA was then transformed into ultra competent E coli cells (XL10 Gold; Stratagene). Transformants were plated out on Q-trays (2000 cfu/tray), picked using a Qbot and archived in 384 well dishes. |
| Fruit | tissue type |
|
