SLC26A4 Break Apart FISH Probe
Empire Genomics’ SLC26A4 Break Apart FISH Probe is designed to flank the SLC26A4 gene and is typically used for detecting SLC26A4 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in orange and green 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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| SLC26A4BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SLC26A4BA-20-AQOR | 20 (40 μL) | 200 μL |
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| SLC26A4BA-20-GOGR | 20 (40 μL) | 200 μL |
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| SLC26A4BA-20-GORE | 20 (40 μL) | 200 μL |
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| SLC26A4BA-20-GRGO | 20 (40 μL) | 200 μL |
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| SLC26A4BA-20-GROR | 20 (40 μL) | 200 μL |
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| SLC26A4BA-20-GRRE | 20 (40 μL) | 200 μL |
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| SLC26A4BA-20-REGO | 20 (40 μL) | 200 μL |
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| SLC26A4BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters. [provided by RefSeq, Jul 2008]
Gene Details
Gene Symbol: SLC26A4
Gene Name: Solute Carrier Family 26 Member 4
Chromosome: CHR7: 107301079-107358252
Locus: 7q22.3
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SLC26A4 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SLC26A4-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping