Methods

Ⅰ  DNA Microarray preparation

A DNA preparation for spotting — Oligo (70 mer, 25 mer miRNA)
cDNA
ORF
B Poly-L-lysine coated slides preparation
C Array design,printing and quality control

Ⅱ  Sample preparation

A RNA isolation and purification
B RNA quality control

Ⅲ  Target Labeling

A Direct incorporation
1. Total RNA direct labeling [Complement] [Short]
2. Total RNA RT labeling check [Complement] [Short]
3. gDNA labeling [Complement] [Short]
4. small RNA labeling [Short]
B Amino allyl-dUTP incorporation
1. Total RNA indirect-labeling [Complement] [Short]
2. mRNA indirect-labeling [Complement] [Short]
3. E.coli RNA indirect-labeling [Complement] [Short]
C Secondary strand cDNA incorporation
2nd cDNA labeling [Complement] [Short]
D Agilent low input amp and labeling [one color]
E 3D labeling ( Genisphere )
3DNA array detection
F Chemical labeling (KREATCH)
1. ULS small RNA labeling
2. ULS aRNA fluorescent labeling

Ⅳ  Hybridization and wash

A Oligonucleotide Arrays on codelink activated slides [MAUI FL ] [MAUI DC]
B cDNA Arrays on Corning GAPSII Slides [GAPSII]
C Agilent [Gene Expression ] [aCGH ] [MAUI A4] [Agilent hybridizer-cRNA] [Agilent hybridizer-cDNA]
D NimbleGen [Gene expression ] [CHIP ] [Methylation ]
E Phalanx [MAUI FL]

Ⅴ  Scanning

A Agilent
B Axon
C TECAN

Ⅵ  Data Analysis

A GeneSpring (GX)
B SAM
C SMD