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GB/T 29582-2013 English PDF

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GB/T 29582-2013English150 Add to Cart 0--9 seconds. Auto-delivery Detection and identification of peanut stunt virus Valid GB/T 29582-2013

PDF similar to GB/T 29582-2013


Standard similar to GB/T 29582-2013

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Basic data

Standard ID GB/T 29582-2013 (GB/T29582-2013)
Description (Translated English) Detection and identification of peanut stunt virus
Sector / Industry National Standard (Recommended)
Classification of Chinese Standard B16
Classification of International Standard 65.020.01
Word Count Estimation 13,153
Quoted Standard SN/T 1840; SN/T 2122
Regulation (derived from) National Standards Bulletin 2013 No. 10
Issuing agency(ies) General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China, Standardization Administration of the People's Republic of China
Summary This standard specifies: peanut stunt virus quarantine and identification methods. This standard applies to live plant material, including vegetative propagation material, tissue culture, seeds and seedlings of peanut stunt virus detection.

GB/T 29582-2013: Detection and identification of peanut stunt virus

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Detection and identification of peanut stunt virus ICS 65.020.01 B16 National Standards of People's Republic of China Identification method of peanut dwarf virus 2013-07-19 release 2013-12-06 implementation General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China China National Standardization Management Committee released

Foreword

This standard is drafted in accordance with the rules given in GB/T 1.1-2009. This standard is proposed by the National Commission for Standardization of Plant Quarantine Standardization (SAC/TC271). The drafting unit of this standard. Shanghai Entry-Exit Inspection and Quarantine Bureau of the People's Republic of China, Shenzhen Entry-Exit Inspection and Quarantine of the People's Republic of China Bureau of the People's Republic of China Xiamen Entry - Exit Inspection and Quarantine Bureau. The main drafters of this standard. Yu Cui, Yang Cuiyun, India Liping, Zheng Yun, Liao Furong, Zheng Jianzhong, Yi Jianping. Identification method of peanut dwarf virus

1 Scope

This standard specifies the method of identification of peanut dwarf virus. This standard applies to the detection of peanut dwarf virus in living plant materials, including asexual propagation material, tissue culture seedlings, seeds and seedlings.

2 normative reference documents

The following documents are indispensable for the application of this document. For dated references, only the dated edition applies to this article Pieces. For undated references, the latest edition (including all modifications) applies to this document. SN/T 1840 Plant virus immunoelectron microscopy SN/T 2122 Quarantine sampling of inbound and outbound plants and plant products

3 peanut dwarf virus basic information

Chinese name. peanut dwarf virus. English name. Peanutstuntvirus. Synonyms. groundnutstuntvirus; peanutstuntcucumovirus; robinia mosaicvirus; cloverblotch virus; peanutcommonmosaicvirus Abbreviations. PSV. Bromoviridae, Cucumber mosaic virus is Cucumovirus. See Appendix A for additional information on peanut dwarf virus.

4 Principle of the method

Using double antibody sandwich enzyme-linked immunosorbent assay based on antigen-antibody response (doubleantibodys and wichenzyme-linked immunosorbentassay, DAS-ELISA), reverse transcription and in vitro DNA synthesis techniques in reverse transcription polymerase chain reaction (reverse transcriptase polymerase chain reaction, RT-PCR). 5 Instruments, facilities, utensils and reagents 5.1 Instruments PCR instrument, clean bench, electronic balance (0.001g), electrophoresis, electrophoresis tank, gel imaging system, electron transmission microscope, water bath Pot, high-speed refrigerated centrifuge, -80 ℃ ultra-low temperature refrigerator, autoclave, ice maker, microwave oven, scroll oscillator. 5.2 facilities Isolated greenhouse (10 ℃ ~ 30 ℃). 5.3 appliances (2 μL, 10 μL, 100 μL,.200 μL, 1000 μL, 5000 μL) and the corresponding RNase-free tip, no RNase centrifuge tube, PCR tube and mortar.