New esophagus cancer markgene RPL 14 and its use
A technology for marker genes and esophageal cancer, applied in the determination/testing of microorganisms, biochemical equipment and methods, etc., can solve problems such as unreported relationships
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0021] Example 1: Method for Detecting RPL14 Gene Deletion
[0022] 1) Extract the peripheral blood of the subject and the DNA of the tissue to be investigated by conventional methods [Molecular Cloning Experiment Guide (Second Edition), J. Sambrook, et al., Cold Spring Harbor Laboratory Press, 1989];
[0023] 2) Use primers R1 and R2 to carry out PCR amplification according to the following conditions:
[0024] R1: 5'AAG CAC CTG GTA CTA AGG GTA 3' (SEQ ID NO: 2)
[0025] R2: 5' TCG CGG CGG TGA TCT TTT TTG 3' (SEQ ID NO: 3)
[0026] PCR reaction system
[0027] Genomic DNA 1.0μl (40ng)
[0028] 10×PCR buffer [100mM Tris-HCl (pH8.3), 500mM KCl] 2.0μl
[0029] 25mM MgCl 2 1.2μl
[0030] 2.5mM dNTP 1.0μl
[0031] Upstream primer (10μM) 1.0μl
[0032] Downstream primer (10μM) 1.0μl
[0033] Deionized formamide 0.5μl
[0034] Taq enzyme (10u / μl) 0.2μl
[0035] Double distilled water 12.1μl
[0036] Total reaction volume 20.0μl
[0...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 