The largest database of trusted experimental protocols

Agilent human whole genome cgh 8 60 k microarray

Manufactured by Agilent Technologies
Sourced in United States

The Agilent Human Whole Genome CGH 8 × 60 K microarray is a microarray platform designed for comparative genomic hybridization (CGH) analysis of the human genome. It contains approximately 60,000 DNA probes that cover the entire human genome, enabling the detection of copy number variations across the genome.

Automatically generated - may contain errors

3 protocols using agilent human whole genome cgh 8 60 k microarray

1

aCGH Genetic Variation Detection

Check if the same lab product or an alternative is used in the 5 most similar protocols
The aCGH was detected genetic variations, including deletions and duplications using the Agilent Human Whole Genome CGH 8 × 60 K microarray (Agilent Technologies, Santa Clara, CA). Test and reference DNA samples were labeled by random priming with either Cy3-dUTP or Cy5-dUTP using the Agilent Genomic DNA Labeling Kit PLUS (Agilent Technologies). All slides were scanned on an Agilent DNA microarray scanner. Data were obtained using the Agilent Feature Extraction Software 9 (Agilent Technologies) and analyzed the ADM-2 statistical algorithms with 6.0 sensitivity thresholds as described previously [15 (link)].
+ Open protocol
+ Expand
2

Genome-wide Copy Number Variation Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Array-based CGH was performed using an Agilent Human Whole Genome CGH 8 × 60 K microarray (Agilent Technologies). Labeling and hybridization were performed using protocols provided by the manufacturer (Cancer Sci. 2013; 104; 631-638). Briefly, 0.5 μg of test or reference DNA was digested with Alu I and Rsa I (Promega, Madison, WI) and purified with the QIAprep Spin Miniprep kit (QIAGEN). Test and reference DNA samples were labeled by random priming with either Cy3-dUTP or Cy5-dUTP using the Agilent Genomic DNA Labeling Kit PLUS (Agilent Technologies). Following the labeling reaction, individually labeled test and reference samples were combined and concentrated using Amicon Ultra-0.5 centrifugal filters (Millipore, Billerica, MA). After denaturing the probe and preannealing it to human Cot-1 DNA, samples were hybridized at 65°C and 20 rpm rotation for 24 hours in a DNA Microarray Hybridization Oven (Agilent Technologies). Samples were washed in wash buffer 1 at room temperature for 5 minutes and wash buffer 2 at 37°C for 1 minute using Agilent Oligo CGH washes. All slides were scanned on an Agilent DNA microarray scanner. Data were obtained using Agilent Feature Extraction Software 9 and analyzed with Agilent CGH Analytics Version 6.5 software using the ADM-2 statistical algorithms with 6.0 sensitivity thresholds.
+ Open protocol
+ Expand
3

Genome-wide Copy Number Variation Detection

Check if the same lab product or an alternative is used in the 5 most similar protocols
The aCGH detected genetic variations, including deletions and duplications, using the Agilent Human Whole Genome CGH 8 × 60 K microarray (Agilent Technologies, Santa Clara, CA, USA). Test and reference DNA samples were labeled by random priming with either Cyanine 3 labeled analog of deoxyuridine triphosphate (dUTP) or Cy5-dUTP using the Agilent Genomic DNA Labeling Kit PLUS (Agilent Technologies). All slides were scanned on an Agilent DNA microarray scanner. Data were obtained using Agilent Feature Extraction Software 9 (Agilent Technologies), which was used to analyze the ADM-2 statistical algorithms with 6.0 sensitivity thresholds, as described previously.19 (link)
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!