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LY/T 2756-2016 English PDF

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LY/T 2756-2016: Molecular identification method for fraxinus varieties with SRAP(sequence-related amplified polymorphism) molecular markers
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LY/T 2756-2016English329 Add to Cart 3 days [Need to translate] Molecular identification method for fraxinus varieties with SRAP(sequence-related amplified polymorphism) molecular markers Valid LY/T 2756-2016

PDF similar to LY/T 2756-2016


Standard similar to LY/T 2756-2016

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Basic data

Standard ID LY/T 2756-2016 (LY/T2756-2016)
Description (Translated English) Molecular identification method for fraxinus varieties with SRAP(sequence-related amplified polymorphism) molecular markers
Sector / Industry Forestry Industry Standard (Recommended)
Classification of Chinese Standard B61
Classification of International Standard 65.020
Word Count Estimation 14,169
Date of Issue 2016-10-19
Date of Implementation 2017-01-01
Regulation (derived from) State Forestry Administration Announcement No 2016 No.19
Issuing agency(ies) State Forestry Administration

LY/T 2756-2016: Molecular identification method for fraxinus varieties with SRAP(sequence-related amplified polymorphism) molecular markers


---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order.
(Molecular identification of waxy varieties) ICS 65.020 B61 People's Republic of China Forestry Industry Standard Molecular identification method for white wax varieties - SRAP molecular marker Released on October 18,.2016 2017-01-01 implementation State Forestry Administration released

Foreword

This standard was drafted in accordance with the rules given in GB/T 1.1-2009. This standard was proposed by the Forestry Department of Liaoning Province. This standard is under the jurisdiction of the State Forestry Administration. This standard was drafted. Liaoning Academy of Forestry, Shenyang Agricultural University, Jinzhou Forestry Research Institute. The main drafters of this standard. Chen Yu, Fan Jungang, Wei Zhongping, Ye Jingfeng, Ma Dongjing, Guo Zhifu, Liu Ping, Liu Yifei, Meng Fanjin, Pan Wenli, Yan Li, Feng Jian, Liu Hongmin, Wang Yuchun, Gao Yingxu, Yang He, Tian Yongxia, Wang Qin, Liu Wei, Yi Hongfeng, Jin Shan, Zhao Lihui. Molecular identification method for white wax varieties - SRAP molecular marker

1 Scope

This standard specifies the operating procedures and analytical methods for the molecular identification method of white wax varieties - SRAP molecular marker method. This standard is applicable to the experimental process of identification of white wax varieties (species) by using the related sequence amplification polymorphism (SRAP) method.

2 Principle

The ash genomic DNA was amplified by designing a pair of primers. The forward primer (F-primer) contains 17 bases, exon Specific amplification was carried out; the reverse primer (R-primer) contained 18 bases, and the intron region and the promoter region were amplified. Due to individual differences And the introns of the species, the promoter and the length of the spacer are different to produce polymorphism. Ultimately by non-denaturing polyacrylamide gel electrophoresis These specific polymorphic fragments were isolated and compared by comparing the differences in the DNA fingerprint bands of the test sample and the control variety. Whether the test sample and the control variety are the same variety.

3 Terms and definitions

The following terms and definitions apply to this document. 3.1 Related sequence polymorphism-relatedamplifiedpolymorphism; SRAP A pair of primers are used to amplify ORFs (openreading frames), a pair of primers including a forward primer and a counter Polymorphisms are generated for primers that differ in their individual size and the length of the intron, promoter and spacer sequences of the species.

4 Instruments and equipment

4.1 PCR instrument. 4.2 Agarose gel electrophoresis system. 4.3 Non-denaturing polyacrylamide gel electrophoresis system. 4.4 Gel imaging system and camera system. 4.5 Ultrapure water system. 4.6 Low temperature high speed refrigerated centrifuge. 4.7 Ultra-micro UV/visible spectrophotometer. 4.8 Autoclave. 4.9 Liquid nitrogen tank. 4.10 Ultra-low temperature refrigerator. 4.11 High-voltage electrophoresis instrument (3000V voltage regulator) and supporting electrophoresis tank. 4.12 Pipette (gun).

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