DGS-C FISH Probe
The DGS-C FISH probe is designed to hybridize to the DGS-C 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 |
|---|---|---|---|---|
| DGCR2-20-OR (Standard Design) | 20 (40 μL) | 200 μL |  |
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| DGCR2-20-RE | 20 (40 μL) | 200 μL |  |
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| DGCR2-20-GO | 20 (40 μL) | 200 μL |  |
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| DGCR2-20-GR | 20 (40 μL) | 200 μL |  |
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| DGCR2-20-AQ | 20 (40 μL) | 200 μL |  |
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| DGCR2-20-DIG | 20 (40 μL) | 200 μL |  |
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| DGCR2-20-BIO | 20 (40 μL) | 200 μL |  |
Gene Summary
Deletions of the 22q11.2 have been associated with a wide range of developmental defects (notably DiGeorge syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome and isolated conotruncal cardiac defects) classified under the acronym CATCH 22. The DGCR2 gene encodes a novel putative adhesion receptor protein, which could play a role in neural crest cells migration, a process which has been proposed to be altered in DiGeorge syndrome. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]
Gene Details
Gene Symbol: DGCR2
Gene Name: DiGeorge Syndrome Critical Region Gene 2
Chromosome: CHR22: 19023794-19109967
Locus: 22q11.21
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|
Customer Publications
Product Details
Product: DGS-C FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: DGCR2-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping