MYH8 FISH Probe
The MYH8 FISH probe is designed to hybridize to the MYH8 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 |
|---|---|---|---|---|
| MYH8-20-OR (Standard Design) | 20 (40 μL) | 200 μL |  |
|
| MYH8-20-RE | 20 (40 μL) | 200 μL |  |
|
| MYH8-20-GO | 20 (40 μL) | 200 μL |  |
|
| MYH8-20-GR | 20 (40 μL) | 200 μL |  |
|
| MYH8-20-AQ | 20 (40 μL) | 200 μL |  |
|
| MYH8-20-DIG | 20 (40 μL) | 200 μL |  |
|
| MYH8-20-BIO | 20 (40 μL) | 200 μL |  |
Gene Summary
Myosins are actin-based motor proteins that function in the generation of mechanical force in eukaryotic cells. Muscle myosins are heterohexamers composed of 2 myosin heavy chains and 2 pairs of nonidentical myosin light chains. This gene encodes a member of the class II or conventional myosin heavy chains, and functions in skeletal muscle contraction. This gene is predominantly expressed in fetal skeletal muscle. This gene is found in a cluster of myosin heavy chain genes on chromosome 17. A mutation in this gene results in trismus-pseudocamptodactyly syndrome. [provided by RefSeq, Sep 2009]
Gene Details
Gene Symbol: MYH8
Gene Name: Myosin Heavy Chain 8
Chromosome: CHR17: 10293641-10325267
Locus: 17p13.1
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|
Customer Publications
Product Details
Product: MYH8 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: MYH8-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping