DGCR6L Break Apart FISH Probe
Empire Genomics’ DGCR6L Break Apart FISH Probe is designed to flank the DGCR6L gene and is typically used for detecting DGCR6L 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 |
|---|---|---|---|---|
| DGCR6LBA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| DGCR6LBA-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| DGCR6LBA-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| DGCR6LBA-20-GORE | 20 (40 μL) | 200 μL |
|
|
| DGCR6LBA-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| DGCR6LBA-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| DGCR6LBA-20-ORGR | 20 (40 μL) | 200 μL |
|
|
| DGCR6LBA-20-REGO | 20 (40 μL) | 200 μL |
|
|
| DGCR6LBA-20-REGR | 20 (40 μL) | 200 μL |
|
Gene Summary
DiGeorge syndrome, and more widely, the CATCH 22 syndrome, are associated with microdeletions in chromosomal region 22q11.2. The product of this gene shares homology with the Drosophila melanogaster gonadal protein, which participates in gonadal and germ cell development, and with the gamma-1 subunit of human laminin. This gene is a candidate for involvement in DiGeorge syndrome pathology and in schizophrenia. [provided by RefSeq, Nov 2008]
Gene Details
Gene Symbol: DGCR6
Gene Name: DiGeorge Syndrome Critical Region Gene 6
Chromosome: CHR22: 18893735-18899601
Locus: 22q11
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|
Customer Publications
Product Details
Product: DGCR6L FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: DGCR6-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping