OPN1SW Break Apart FISH Probe
Empire Genomics’ OPN1SW Break Apart FISH Probe is designed to flank the OPN1SW gene and is typically used for detecting OPN1SW 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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| OPN1SWBA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| OPN1SWBA-20-AQOR | 20 (40 μL) | 200 μL |
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| OPN1SWBA-20-GOGR | 20 (40 μL) | 200 μL |
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| OPN1SWBA-20-GORE | 20 (40 μL) | 200 μL |
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| OPN1SWBA-20-GRGO | 20 (40 μL) | 200 μL |
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| OPN1SWBA-20-GRRE | 20 (40 μL) | 200 μL |
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| OPN1SWBA-20-ORGR | 20 (40 μL) | 200 μL |
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| OPN1SWBA-20-REGO | 20 (40 μL) | 200 μL |
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| OPN1SWBA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This gene belongs to the G-protein coupled receptor 1 family, opsin subfamily. It encodes the blue cone pigment gene which is one of three types of cone photoreceptors responsible for normal color vision. Defects in this gene are the cause of tritan color blindness (tritanopia). Affected individuals lack blue and yellow sensory mechanisms while retaining those for red and green. Defective blue vision is characteristic. [provided by RefSeq, Jul 2008]
Gene Details
Gene Symbol: OPN1SW
Gene Name: Opsin 1, Short Wave Sensitive
Chromosome: CHR7: 128412542-128415844
Locus: 7q32.1
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: OPN1SW FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: OPN1SW-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping