NPHP4 Break Apart FISH Probe
Empire Genomics’ NPHP4 Break Apart FISH Probe is designed to flank the NPHP4 gene and is typically used for detecting NPHP4 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in green and orange 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 |
|---|---|---|---|---|
| NPHP4BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| NPHP4BA-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| NPHP4BA-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| NPHP4BA-20-GORE | 20 (40 μL) | 200 μL |
|
|
| NPHP4BA-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| NPHP4BA-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| NPHP4BA-20-ORGR | 20 (40 μL) | 200 μL |
|
|
| NPHP4BA-20-REGO | 20 (40 μL) | 200 μL |
|
|
| NPHP4BA-20-REGR | 20 (40 μL) | 200 μL |
|
Gene Summary
This gene encodes a protein involved in renal tubular development and function. This protein interacts with nephrocystin, and belongs to a multifunctional complex that is localized to actin- and microtubule-based structures. Mutations in this gene are associated with nephronophthisis type 4, a renal disease, and with Senior-Loken syndrome type 4, a combination of nephronophthisis and retinitis pigmentosa. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]
Gene Details
Gene Symbol: NPHP4
Gene Name: Nephrocystin 4
Chromosome: CHR1: 5922869-6052533
Locus: 1p36.31
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|
Customer Publications
Product Details
Product: NPHP4 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: NPHP4-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping