SurePrint G3 Human Genome Catalog CNV Microarray Kits

SurePrint G3 Human Genome Catalog CNV Microarray Kits

Available in 1M and 400K formats.

Microarray-based Comparative Genomic Hybridization (aCGH) is a powerful technique used to identify and characterize DNA copy number variations across the genome. Using array-based comparative genomic hybridization (aCGH) techniques, copy number variants (CNVs) at multiple loci can be assessed simultaneously, allowing for their identification and characterization. Agilent’s SurePrint G3 CNV microarrays provide high-resolution and optimized probe design for maximal sensitivity and specificity. Simplified protocols further streamline processing of complex analysis, while maintaining the quality and reliability that your research demands.

Features

Product NameSurePrint G3 Human Genome Catalog CNV Microarray
Agilent Part Number1M: G4506A
400K: G4507A
Design ID1M: 023642
400K: 021365
Format1M: 1x1M
200K: 2x400K
Arrays/Slide1M: 1
400K: 2
Slide/Kit1M: 5
400K: 5
Sequences1M: 963,000+ human sequences
400K: 412,000+ human sequences
Probes1M: 2.6 KB overall median probe spacing, 3 KB average probe spacing
400K: 1 KB overall median probe spacing (1 KB in CNVs)
CompositionInput amount varies by format (minimum 0.5 μg total genomic DNA input requirement)
Probes annotated against NCBI Build 36 (UCSC hg18, March 2006)
Permitted UseResearch Use Only
Product LiteratureaCGH Protocol with Enzymatic Labeling for Blood, Cells, or Tissues

aCGH Protocol with ULS Labeling for Blood, Cells, Tissues, or FFPE

Agilent’s Copy Number Variation (CNV) Portfolio

CGH Application Brochure

A Robust Whole Genome Amplification Method for Agilent Array-based Comparative Genome Hybridization Analysis

Bravo Automated Liquid Handling Platform Protocol with Enzymatic and ULS Labeling

Automating the CGH/CNV Workflow with the Bravo Automated Liquid Handling Platform