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ClearSeq Inherited Disease, XT
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Regulatory Status:
RUO
The ClearSeq Inherited Disease enables analysis of 2,742 genes known to cause inherited disorders.
Ultimate Union kits, part of Agilent's capillary flow technology family, provide extremely low dead volume column connections.
ClearSeq Inherited Disease Data Sheet
- Publication Part Number: 5991-4962EN
- Created: 16 July 2014
- 427 KB
| Chinese (Simplified) (China) | Complete (PDF) |
|---|
Protocol for SureSelect XT HS2 RNA Library Preparation and Target Enrichment for the Illumina platform.
- Publication Part Number: G9989-90000
- Created: 16 May 2023
- 2 MB
SureSelect Target Enrichment System for Sequencing on Ion Proton Protocol
- Publication Part Number: G7530-90005
- Created: 23 Aug 2021
- 633 KB
SureSelect QXT Target Enrichment for Illumina Multiplexed Sequencing Protocol
- Publication Part Number: G9681-90000
- Created: 29 July 2021
- 800 KB
SureSelect XT Target Enrichment System for the Illumina Platform Protocol
- Publication Part Number: G7530-90000
- Created: 29 July 2021
- 1 MB
- Released: 05 Apr 2022
- 267 KB
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