CHD7 FISH Probe
Our CHD7 probe is designed to detect CHD7 amplifications and deletions. The probe comes labeled in orange, but can be customized to meet your needs.
** This product is for in vitro and research use only. This product is not intended for diagnostic use.
Turnaround Time: 7-10 Business Days Shipping Time: 1-2 Day Expedited Shipping
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| CHD7-20-OR (Standard Design) | 20 (40 μL) | 200 μL |
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| CHD7-20-RE | 20 (40 μL) | 200 μL |
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| CHD7-20-AQ | 20 (40 μL) | 200 μL |
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| CHD7-20-GR | 20 (40 μL) | 200 μL |
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| CHD7-20-GO | 20 (40 μL) | 200 μL |
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Gene Summary
This gene encodes a protein that contains several helicase family domains. Mutations in this gene have been found in some patients with the CHARGE syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]
Gene Details
Gene Symbol: CHD7
Gene Name: Chromodomain Helicase DNA Binding Protein 7
Chromosome: CHR8: 61591323-61780586
Locus: 8q12.2
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
There are currently no FISH related publications for this gene.