SLC4A11 Break Apart FISH Probe
Empire Genomics’ SLC4A11 Break Apart FISH Probe is designed to flank the SLC4A11 gene and is typically used for detecting SLC4A11 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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| SLC4A11BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| SLC4A11BA-20-AQOR | 20 (40 μL) | 200 μL |
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| SLC4A11BA-20-GOGR | 20 (40 μL) | 200 μL |
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| SLC4A11BA-20-GORE | 20 (40 μL) | 200 μL |
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| SLC4A11BA-20-GRGO | 20 (40 μL) | 200 μL |
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| SLC4A11BA-20-GRRE | 20 (40 μL) | 200 μL |
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| SLC4A11BA-20-ORGR | 20 (40 μL) | 200 μL |
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| SLC4A11BA-20-REGO | 20 (40 μL) | 200 μL |
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| SLC4A11BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This gene encodes a voltage-regulated, electrogenic sodium-coupled borate cotransporter that is essential for borate homeostasis, cell growth and cell proliferation. Mutations in this gene have been associated with a number of endothelial corneal dystrophies including recessive corneal endothelial dystrophy 2, corneal dystrophy and perceptive deafness, and Fuchs endothelial corneal dystrophy. Multiple transcript variants encoding different isoforms have been described. [provided by RefSeq, Mar 2010]
Gene Details
Gene Symbol: SLC4A11
Gene Name: Solute Carrier Family 4 Member 11
Chromosome: CHR20: 3208062-3219887
Locus: 20p13
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SLC4A11 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SLC4A11-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping