CSNB1D FISH Probe
The CSNB1D FISH probe is designed to hybridize to the CSNB1D 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 |
|---|---|---|---|---|
| SLC24A1-20-OR (Standard Design) | 20 (40 μL) | 200 μL |  |
|
| SLC24A1-20-RE | 20 (40 μL) | 200 μL |  |
|
| SLC24A1-20-GO | 20 (40 μL) | 200 μL |  |
|
| SLC24A1-20-GR | 20 (40 μL) | 200 μL |  |
|
| SLC24A1-20-AQ | 20 (40 μL) | 200 μL |  |
|
| SLC24A1-20-DIG | 20 (40 μL) | 200 μL |  |
|
| SLC24A1-20-BIO | 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: CSNB1D 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