SCNN1B Break Apart FISH Probe
Empire Genomics’ SCNN1B Break Apart FISH Probe is designed to flank the SCNN1B gene and is typically used for detecting SCNN1B 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 |
|---|---|---|---|---|
| SCNN1BBA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| SCNN1BBA-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| SCNN1BBA-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| SCNN1BBA-20-GORE | 20 (40 μL) | 200 μL |
|
|
| SCNN1BBA-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| SCNN1BBA-20-GROR | 20 (40 μL) | 200 μL |
|
|
| SCNN1BBA-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| SCNN1BBA-20-REGO | 20 (40 μL) | 200 μL |
|
|
| SCNN1BBA-20-REGR | 20 (40 μL) | 200 μL |
|
Gene Summary
Nonvoltage-gated, amiloride-sensitive, sodium channels control fluid and electrolyte transport across epithelia in many organs. These channels are heteromeric complexes consisting of 3 subunits: alpha, beta, and gamma. This gene encodes the beta subunit, and mutations in this gene have been associated with pseudohypoaldosteronism type 1 (PHA1), and Liddle syndrome. [provided by RefSeq, Apr 2009]
Gene Details
Gene Symbol: SCNN1B
Gene Name: Sodium Channel Epithelial 1 Beta Subunit
Chromosome: CHR16: 23313590-23392620
Locus: 16p12.2
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|
Customer Publications
Product Details
Product: SCNN1B FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SCNN1B-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping