CNE4 Break Apart FISH Probe
Empire Genomics’ CNE4 Break Apart FISH Probe is designed to flank the CNE4 gene and is typically used for detecting CNE4 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in green and orange by default, but may be customized to meet your needs.
** This product is for in vitro and research use only. This product is not intended for diagnostic use.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| CNE4BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| CNE4BA-20-AQOR | 20 (40 μL) | 200 μL |
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| CNE4BA-20-GOGR | 20 (40 μL) | 200 μL |
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| CNE4BA-20-GORE | 20 (40 μL) | 200 μL |
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| CNE4BA-20-GRGO | 20 (40 μL) | 200 μL |
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| CNE4BA-20-GRRE | 20 (40 μL) | 200 μL |
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| CNE4BA-20-ORGR | 20 (40 μL) | 200 μL |
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| CNE4BA-20-REGO | 20 (40 μL) | 200 μL |
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| CNE4BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This genomic element is found within the pseudoautosomal region 1 (PAR1) of chromosomes X and Y, where each chromosome contains the same DNA region. It is located approximately 94 kb downstream of the SHOX (short stature homeobox) gene, and is one of several conserved elements that surround that gene. It can function as an enhancer of SHOX gene expression. Mutations that include this element, including deletions and microduplications, are associated with Leri-Weill dyschondrosteosis (LWD) and idiopathic short stature (ISS), and they have also been implicated in autism spectrum disorders (ASDs) and related neurodevelopmental conditions. [provided by RefSeq, Jul 2016]
Gene Details
Gene Symbol: CNE4
Gene Name: CNE4 Enhancer Downstream Of SHOX
Locus: Xp22.33; Yp11.3
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: CNE4 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: CNE4-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping