WHCR FISH Probe
The WHCR FISH probe is designed to hybridize to the WHCR 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 |
|---|---|---|---|---|
| WHCR-20-OR (Standard Design) | 20 (40 μL) | 200 μL |  |
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| WHCR-20-RE | 20 (40 μL) | 200 μL |  |
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| WHCR-20-GO | 20 (40 μL) | 200 μL |  |
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| WHCR-20-GR | 20 (40 μL) | 200 μL |  |
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| WHCR-20-AQ | 20 (40 μL) | 200 μL |  |
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| WHCR-20-DIG | 20 (40 μL) | 200 μL |  |
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| WHCR-20-BIO | 20 (40 μL) | 200 μL |  |
Gene Summary
Wolf-Hirschhorn syndrome is a congenital malformation syndrome characterized by pre- and postnatal growth deficiency, developmental disability of variable degree, characteristic craniofacial features ('Greek warrior helmet' appearance of the nose, high forehead, prominent glabella, hypertelorism, high-arched eyebrows, protruding eyes, epicanthal folds, short philtrum, distinct mouth with downturned corners, and micrognathia), and a seizure disorder (Battaglia et al., 2008 [PubMed 18932224]).[supplied by OMIM, Nov 2010]
Gene Details
Gene Symbol: WHCR
Gene Name: Wolf-Hirschhorn Syndrome Chromosome Region
Locus: 4p16
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: WHCR FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: WHCR-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping