EVC2 Break Apart FISH Probe
Empire Genomics’ EVC2 Break Apart FISH Probe is designed to flank the EVC2 gene and is typically used for detecting EVC2 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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| EVC2BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| EVC2BA-20-AQOR | 20 (40 μL) | 200 μL |
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| EVC2BA-20-GOGR | 20 (40 μL) | 200 μL |
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| EVC2BA-20-GORE | 20 (40 μL) | 200 μL |
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| EVC2BA-20-GRGO | 20 (40 μL) | 200 μL |
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| EVC2BA-20-GRRE | 20 (40 μL) | 200 μL |
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| EVC2BA-20-ORGR | 20 (40 μL) | 200 μL |
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| EVC2BA-20-REGO | 20 (40 μL) | 200 μL |
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| EVC2BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This gene encodes a protein that functions in bone formation and skeletal development. Mutations in this gene, as well as in a neighboring gene that lies in a head-to-head configuration, cause Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia that is also known as chondroectodermal dysplasia. Mutations in this gene also cause acrofacial dysostosis Weyers type, also referred to as Curry-Hall syndrome, a disease that combines limb and facial abnormalities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
Gene Details
Gene Symbol: EVC2
Gene Name: EvC Ciliary Complex Subunit 2
Chromosome: CHR4: 5564145-5711275
Locus: 4p16.2
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: EVC2 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: EVC2-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping