Community Designs Prenatal Research Microarray
RUO
Agilent Community Designs offer dedicated tools for the analysis of prenatal samples developed by or in collaboration with experts. Chromosomal microarrays enable focused genomic analysis, combining Agilent oligo quality with focused targets defined by scientists working in prenatal research..
Agilent has not performed verification and validation on these panels
Agilent has not performed verification and validation on these panels
For Research Use Only. Not for use in diagnostic procedures.
- ACD Microarrays
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This product is not available for purchase by the general public.
Product Details
Features
- Content developed by experts in the industry
- Easy ordering process - no minimum order
- All the arrays are produced made-to-order
- Agilent oligo quality – same as any standard catalog design
Specifications
| Area of Research |
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| Arrays per Slide |
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| Composition Genome |
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| Slides per Kit |
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| Species |
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Literature
- Flyers
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SurePrint Community Design Prenatal CGH+SNP 8X60K Microarray Flyer
Flyer for new SurePrint Community Design Prenatal CGH+SNP 8X60K Mircroarray
- Flyers
- English
- 07 Jul 2021
- 266.08 KB
SurePrint Community Design Prenatal EasyChip 8x15K
Chromosomal microarray for prenatal research
- Flyers
- English
- 17 Jul 2020
- 305.29 KB
Support
- User Manuals
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Quick Reference Guide for 8x Arrays - Oligonucleotide Array-Based CGH for Genomic DNA
A quick reference guide for processing 8-pack aCGH microarrays using enzymatic labeling of gDNA from blood, cells, or tissues.
- User Manuals
- English
- 01 Apr 2020
- 164.20 KB
Oligonucleotide aCGH for gDNA Analysis - Enzymatic Labeling For Blood, Cells, or Tissues (with a High Throughput option)
Oligonucleotide Array-Based CGH for Genomic DNA Analysis - Enzymatic Labeling For Blood, Cells, or Tissues (with a High Throughput option) Protocol
- User Manuals
- English
- 04 Mar 2020
- 4.63 MB
Featured References
- Publications
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- Alesi V, Bernardini L, Goidin D, Canestrelli M, Dentici ML, et al. (2015) Easychip 8x15k: A New Tool for Detecting Chromosome Anomalies in Low Risk Pregnancies, Supporting and Integrating Standard Karyotype. J Genet Syndr Gene Ther 7: 277. doi:10.4172/2157-7412.1000277 Learn More
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