SMCR8 FISH Probe
The SMCR8 FISH probe is designed to hybridize to the SMCR8 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 |
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SMCR8-20-OR (Standard Design) | 20 (40 μL) | 200 μL | ||
SMCR8-20-RE | 20 (40 μL) | 200 μL | ||
SMCR8-20-GO | 20 (40 μL) | 200 μL | ||
SMCR8-20-GR | 20 (40 μL) | 200 μL | ||
SMCR8-20-AQ | 20 (40 μL) | 200 μL | ||
SMCR8-20-DIG | 20 (40 μL) | 200 μL | ||
SMCR8-20-BIO | 20 (40 μL) | 200 μL |
Gene Summary
The Smith-Magenis Syndrome Chromosome Region, Candidate 8 (SMCR8) gene is located on chr17:18218593 -18231370 at 17p11.2.
Gene Details
Gene Symbol: SMCR8
Gene Name: Smith-Magenis Syndrome Chromosome Region, Candidate 8
Chromosome: CHR17: 18218593-18231370
Locus: 17p11.2
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SMCR8 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SMCR8-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping