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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.

Turnaround Time: 7-10 Business Days    Shipping Time: 1-2 Day Expedited Shipping

SKU Test Kits Buffer Dye Color Order Now
C16DELQ22-20-OR  (Standard Design) 20 (40 μL) 200 μL
C16DELQ22-20-RE 20 (40 μL) 200 μL
C16DELQ22-20-GO 20 (40 μL) 200 μL
C16DELQ22-20-GR 20 (40 μL) 200 μL
C16DELQ22-20-AQ 20 (40 μL) 200 μL
C16DELQ22-20-DIG 20 (40 μL) 200 μL
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

There are currently no FISH related publications for this gene.

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