SLC26A4 FISH Probe
The SLC26A4 FISH probe is designed to hybridize to the SLC26A4 gene and is primarily used for detecting amplifications and deletions associated with the gene. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe can be labeled in one of five colors. Each probe is sold in a 20 test kit (approximately 20 slides - 22x22 mm area) and includes hybridization buffer. Please note that due to design optimizations, prices are subject to change.
** 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 |
|---|---|---|---|---|
| SLC26A4-20-OR (Standard Design) | 20 (40 μL) | 200 μL |  |
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| SLC26A4-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC26A4-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC26A4-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC26A4-20-AQ | 20 (40 μL) | 200 μL |  |
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| SLC26A4-20-DIG | 20 (40 μL) | 200 μL |  |
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| SLC26A4-20-BIO | 20 (40 μL) | 200 μL |  |
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