MSX2 Break Apart FISH Probe
Empire Genomics’ MSX2 Break Apart FISH Probe is designed to flank the MSX2 gene and is typically used for detecting MSX2 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 |
|---|---|---|---|---|
| MSX2BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| MSX2BA-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| MSX2BA-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| MSX2BA-20-GORE | 20 (40 μL) | 200 μL |
|
|
| MSX2BA-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| MSX2BA-20-GROR | 20 (40 μL) | 200 μL |
|
|
| MSX2BA-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| MSX2BA-20-REGO | 20 (40 μL) | 200 μL |
|
|
| MSX2BA-20-REGR | 20 (40 μL) | 200 μL |
|
Gene Summary
This gene encodes a member of the muscle segment homeobox gene family. The encoded protein is a transcriptional repressor whose normal activity may establish a balance between survival and apoptosis of neural crest-derived cells required for proper craniofacial morphogenesis. The encoded protein may also have a role in promoting cell growth under certain conditions and may be an important target for the RAS signaling pathways. Mutations in this gene are associated with parietal foramina 1 and craniosynostosis type 2. [provided by RefSeq, Jul 2008]
Gene Details
Gene Symbol: MSX2
Gene Name: Msh Homeobox 2
Chromosome: CHR5: 174151574-174157902
Locus: 5q35.2
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|
Customer Publications
Product Details
Product: MSX2 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: MSX2-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping