Related Experiment Video

Updated: May 13, 2026

Novel Sequence Discovery by Subtractive Genomics
09:40

Novel Sequence Discovery by Subtractive Genomics

Published on: January 25, 2019

[Full-length cDNA clone and sequence analysis of Cu/Zn-SOD gene from Evodia rutaecarpa]

Bo Wu1, Guang-ming Luo, Dan Gao

  • 1Chinese Medicine Germplasm Resource Engineering Technology Research Center,Jiangxi University of Traditional Chinese Medicine, Nanchang 330004, China. wubojxtcmi@sina.com

Zhong Yao Cai = Zhongyaocai = Journal of Chinese Medicinal Materials
|March 5, 2013
PubMed
Abstract

More Related Videos

Small-Scale Extraction of Caenorhabditis elegans Genomic DNA06:40

Small-Scale Extraction of Caenorhabditis elegans Genomic DNA

Published on: June 7, 2022

An Array-based Comparative Genomic Hybridization Platform for Efficient Detection of Copy Number Variations in Fast Neutron-induced Medicago truncatula Mutants09:32

An Array-based Comparative Genomic Hybridization Platform for Efficient Detection of Copy Number Variations in Fast Neutron-induced Medicago truncatula Mutants

Published on: November 8, 2017

Related Concept Videos

Cis-regulatory Sequences02:02

Cis-regulatory Sequences

Cis-regulatory sequences are short fragments of non-coding DNA that are present on the same chromosomes as the genes that they regulate. These fragments serve as binding sites for transcriptional regulators, proteins that are responsible for controlling gene transcription and differential gene expression across cell types in eukaryotes. Cis-regulatory sequences can be close to the gene of interest or thousands of bases away in the DNA sequence; however, those sequences that are further away are...
RACE - Rapid Amplification of cDNA Ends02:35

RACE - Rapid Amplification of cDNA Ends

Rapid Amplification of cDNA Ends, or RACE, is one of the most effective methods to obtain a full-length cDNA from an mRNA sequence between a known internal region to the unknown sequence at the 5’ or 3’ end. The unknown region is cloned in the cDNA by a gene-specific primer that binds the known end, and a hybrid primer that attaches a predefined anchor sequence to the unknown end of the cDNA. The sequence in between is amplified by PCR with an anchor primer and a gene-specific primer.
Since the...