SLC9A6 Break Apart FISH Probe
Empire Genomics’ SLC9A6 Break Apart FISH Probe is designed to flank the SLC9A6 gene and is typically used for detecting SLC9A6 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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| SLC9A6BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SLC9A6BA-20-AQOR | 20 (40 μL) | 200 μL |
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| SLC9A6BA-20-GOGR | 20 (40 μL) | 200 μL |
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| SLC9A6BA-20-GORE | 20 (40 μL) | 200 μL |
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| SLC9A6BA-20-GRGO | 20 (40 μL) | 200 μL |
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| SLC9A6BA-20-GROR | 20 (40 μL) | 200 μL |
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| SLC9A6BA-20-GRRE | 20 (40 μL) | 200 μL |
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| SLC9A6BA-20-REGO | 20 (40 μL) | 200 μL |
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| SLC9A6BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This gene encodes a sodium-hydrogen exchanger that is amember of the solute carrier family 9. The encoded protein localizes to early and recycling endosomes and may be involved in regulating endosomal pH and volume. Defects in this gene are associated with X-linked syndromic cognitive disability, Christianson type. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Apr 2010]
Gene Details
Gene Symbol: SLC9A6
Gene Name: Solute Carrier Family 9 Member A6
Chromosome: CHRX: 135067582-135129428
Locus: Xq26.3
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SLC9A6 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SLC9A6-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping