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DNA probes are fragments of DNA labeled with a reporter tag to enable their detection or purification. The resulting labeled DNA probes can then hybridize to target nucleic acid sequences through complementary base-pairing, and may be used to recover or identify these regions.
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Related Experiment Video

Updated: Oct 20, 2025

Extraction of Venom and Venom Gland Microdissections from Spiders for Proteomic and Transcriptomic Analyses
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Snake Venom Identification via Fluorescent Discrimination.

Fei Chen1, Meng Qin2, Wei Liu3

  • 1College of Chemistry and Materials Science, Guangdong Provincial Key Laboratory of Functional Supramolecular Coordination Materials and Applications, Guangdong Engineering & Technology Research Centre of Graphene-like Materials and Products, Jinan University, Guangzhou 510632, China.

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A novel fluorescent sensor array effectively identifies and differentiates snake venoms, aiding rapid clinical diagnosis. This technology accurately analyzes complex venom components and mixtures, improving patient treatment outcomes.

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Area of Science:

  • Biochemistry
  • Analytical Chemistry
  • Toxicology

Background:

  • Accurate snake venom identification is crucial for effective clinical treatment.
  • The complex composition of snake venom presents significant challenges for rapid and precise analysis.
  • Existing methods may lack the speed or accuracy required for timely diagnosis.

Purpose of the Study:

  • To develop a novel fluorescent sensor array for the rapid and accurate identification and discrimination of snake venoms.
  • To mimic the principles of biological taste sensing for enhanced venom detection.
  • To assess the sensor array's performance in complex biological matrices and with potential interferents.

Main Methods:

  • Fabrication of a multi-fluorescent dye sensor array.
  • Utilizing the differential interaction of snake venom components with fluorescent dyes to generate a unique response signature.
  • Testing the sensor array's ability to identify specific venom proteins, differentiate various snake venoms, and analyze samples in buffer and human plasma.

Main Results:

  • The sensor array achieved 100% accuracy in identifying six main snake venom proteins at various concentrations and in mixtures.
  • Seven distinct snake venoms from different families were successfully discriminated in both PBS buffer and human plasma.
  • The sensor array demonstrated practicality by distinguishing venoms in the presence of common biological interferents like bovine serum albumin (BSA), thrombin, and transferrin (TRF).

Conclusions:

  • The developed fluorescent sensor array offers an effective strategy for rapid and accurate snake venom toxicology analysis.
  • This multi-response sensor array technology has significant potential to benefit early and timely clinical diagnosis and treatment of snakebites.
  • The findings highlight the promise of bio-inspired sensor systems for complex analytical challenges in clinical toxicology.