The pruning period of grapes in winter is 2 to 3 weeks after the plants are naturally deciduous and before the bleeding, usually in December. In general, the germination rate and seed setting rate at the base of the parent branch of grapes are lower, while the middle and upper bud eyes are higher. For varieties with vigorous growth and low fruiting female shoots, medium and long shoots are mainly pruned; the flower buds at the lower part of weak branches are better differentiated, and short shoots are the main pruning method. For the pruning of Kyoho, Hongdi, and Qiuli grapes, the pruning method is mainly mid-top pruning, with a mixture of long and short shoots. For the pruning of the fruiting mother branches, 4 to 8 buds are generally left when using mid-shoot pruning; when using short-shoot pruning, 2 to 3 buds are left, and when long-shoot pruning, 8-12 buds are left. For specific pruning, leave branches with full buds and tight scales, dense tissues, short internodes, large internodes protruding, deep purple in color and fully mature branches without pests and diseases. As for the number of pruning parent branches, it can be judged according to the comprehensive factors such as variety characteristics, shelf characteristics, tree age, and yield. Generally, 8 to 10 fruiting parent branches are reserved per square meter on the shelf surface of the fence, and 6 to 8 fruiting parent branches per square meter on the shelf surface.
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Nucleic Acid Extraction Reagent Kit 96T(auto)
[Intended Use]
Extraction, enrichment, purification of nucleic acid. The processed products can be applied in clinical in vitro detection.
[Testing Principle]
During the nucleic acid extraction process, the magnetic bead adsorption principle is used to adsorb, transfer, and purify nucleic acids through special magnetic beads to automatically complete the nucleic acid extraction.
[Storage and Expiry date]
It could be stored at room temperature.
Expiry date is 12 months.
[Product Features]
1. Efficient extraction of high quality RNA.
2. Rapid purification to obtain high-quality, ready-to-use RNA.
3. Good repeatability and high output.
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