C16DELQ22 FISH Probe
The C16DELQ22 FISH probe is designed to hybridize to the C16DELQ22 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 |
|---|---|---|---|---|
| C16DELQ22-20-OR (Standard Design) | 20 (40 μL) | 200 μL |  |
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| C16DELQ22-20-RE | 20 (40 μL) | 200 μL |  |
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| C16DELQ22-20-GO | 20 (40 μL) | 200 μL |  |
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| C16DELQ22-20-GR | 20 (40 μL) | 200 μL |  |
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| C16DELQ22-20-AQ | 20 (40 μL) | 200 μL |  |
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| C16DELQ22-20-DIG | 20 (40 μL) | 200 μL |  |
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| C16DELQ22-20-BIO | 20 (40 μL) | 200 μL |  |
Gene Details
Gene Symbol: C16DELQ22
Gene Name: Chromosome 16q22 Deletion Syndrome
Locus: 16q22
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|
Customer Publications
Product Details
Product: C16DELQ22 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: C16DELQ22-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping