Related Experiment Video
Updated: Aug 6, 2026

07:40
A Noninvasive Hair Sampling Technique to Obtain High Quality DNA from Elusive Small Mammals
Published on: March 13, 2011
DNA profiling of shahtoosh
James Chun-I Lee1, Li-Chin Tsai, Chung-Yu Yang
1Department of Forensic Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan, ROC.
Electrophoresis
|August 5, 2006
Summary
DNA profiling of shahtoosh shawls can identify Tibetan Antelope (Pantholops hodgsonii) wool. This method aids in detecting illegal wildlife trade and protecting endangered species like the Tibetan Antelope.
Area of Science:
- Conservation genetics
- Wildlife forensics
Background:
- Tibetan Antelope (Pantholops hodgsonii) populations are declining due to illegal poaching for shahtoosh wool.
- Shahtoosh, made from fine Tibetan Antelope wool, is highly valued, leading to endangerment and CITES Appendix I listing.
Purpose of the Study:
- To develop a DNA profiling method for identifying Tibetan Antelope wool in shahtoosh products.
- To establish a reliable test for detecting P. hodgsonii in confiscated items.
Main Methods:
- DNA was extracted from two shahtoosh samples and ten comparative wool samples (sheep, cashmere, pashmina).
- A 271 bp fragment of the cytochrome b (cyt b) gene was amplified using specific primers.
- Amplified DNA fragments were sequenced and compared to GenBank and EMBL databases.
Main Results:
- DNA typing successfully identified the species of origin for all wool samples.
- Sequencing confirmed high homology with known cyt b genes of P. hodgsonii, Capra hircus, and Ovis aries.
- Sufficient DNA was present in finished shahtoosh wool for successful typing.
Conclusions:
- A DNA profiling method using the cyt b gene can unambiguously identify Tibetan Antelope wool in shahtoosh.
- This technique is a plausible tool for identifying CITES-protected species and combating illegal wildlife trade.
Related Concept Videos
Pedigree Analysis
Overview
Pedigree Analysis
Overview
Modern Molecular Taxonomy
Advancements in molecular biology have revolutionized the identification and characterization of bacteria, with multiple methods leveraging DNA sequencing for enhanced precision. As sequencing technologies improve and costs decline, these approaches are increasingly used in clinical, environmental, and evolutionary studies.Multilocus Sequence Typing (MLST) examines several housekeeping genes, essential chromosomal genes encoding cellular functions, to distinguish strains. Approximately...
DNA Microarrays
Microarrays are high-throughput and relatively inexpensive assays that can be automated to analyze large quantities of data at a time. They are used in genome-wide studies to compare gene or protein expression under two varied conditions, such as healthy and diseased states. Microarrays consist of glass or silica slides on which probe molecules are covalently attached through surface functionalization. Most commonly, the slides are prepared through the chemisorption of silanes to silica...
Southern Blot
Agarose gel electrophoresis is very useful in separating DNA fragments by size. Running a DNA ladder containing fragments of the known length alongside the sample helps determine the approximate length of the sample DNA fragments. However, additional steps are needed to verify the sequence identity of the sample DNA fragments.
Denatured DNA fragments must be transferred onto a carrier membrane from the gel to make it accessible to a probe - a small ssDNA fragment complementary to the target DNA...
Denatured DNA fragments must be transferred onto a carrier membrane from the gel to make it accessible to a probe - a small ssDNA fragment complementary to the target DNA...
DNA Isolation
DNA isolation protocols can be fast and straightforward or complex and time-consuming depending on the type and quality of DNA required for further processing. For example, plasmid DNA extraction is a bit more complicated than genomic DNA extraction because of the need for an appropriate lysis method to separate plasmid DNA from gDNA during isolation. However, for specific applications, such as long-range DNA sequencing that require a good yield of high- quality DNA samples, we need to follow...
