SLC24A1 Break Apart FISH Probe
Empire Genomics’ SLC24A1 Break Apart FISH Probe is designed to flank the SLC24A1 gene and is typically used for detecting SLC24A1 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 |
---|---|---|---|---|
SLC24A1BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
SLC24A1BA-20-AQOR | 20 (40 μL) | 200 μL | ||
SLC24A1BA-20-GOGR | 20 (40 μL) | 200 μL | ||
SLC24A1BA-20-GORE | 20 (40 μL) | 200 μL | ||
SLC24A1BA-20-GRGO | 20 (40 μL) | 200 μL | ||
SLC24A1BA-20-GROR | 20 (40 μL) | 200 μL | ||
SLC24A1BA-20-GRRE | 20 (40 μL) | 200 μL | ||
SLC24A1BA-20-REGO | 20 (40 μL) | 200 μL | ||
SLC24A1BA-20-REGR | 20 (40 μL) | 200 μL |
Gene Summary
This gene encodes a member of the potassium-dependent sodium/calcium exchanger protein family. The encoded protein plays an important role in sodium/calcium exchange in retinal rod and cone photoreceptors by mediating the extrusion of one calcium ion and one potassium ion in exchange for four sodium ions. Mutations in this gene may play a role in congenital stationary night blindness. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]
Gene Details
Gene Symbol: SLC24A1
Gene Name: Solute Carrier Family 24 Member 1
Chromosome: CHR15: 65914269-65948598
Locus: 15q22.31
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
---|
Customer Publications
Product Details
Product: SLC24A1 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SLC24A1-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping