FTHS FISH Probe
The FTHS FISH probe is designed to hybridize to the FTHS 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 |
|---|---|---|---|---|
| SH3PXD2B-20-OR (Standard Design) | 20 (40 μL) | 200 μL |  |
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| SH3PXD2B-20-RE | 20 (40 μL) | 200 μL |  |
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| SH3PXD2B-20-GO | 20 (40 μL) | 200 μL |  |
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| SH3PXD2B-20-GR | 20 (40 μL) | 200 μL |  |
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| SH3PXD2B-20-AQ | 20 (40 μL) | 200 μL |  |
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| SH3PXD2B-20-DIG | 20 (40 μL) | 200 μL |  |
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| SH3PXD2B-20-BIO | 20 (40 μL) | 200 μL |  |
Gene Summary
This gene encodes an adapter protein that is characterized by a PX domain and four Src homology 3 domains. The encoded protein is required for podosome formation and is involved in cell adhesion and migration of numerous cell types. Mutations in this gene are the cause of Frank-ter Haar syndrome (FTHS), and also Borrone Dermato-Cardio-Skeletal (BDCS) syndrome. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2015]
Gene Details
Gene Symbol: SH3PXD2B
Gene Name: SH3 And PX Domains 2B
Chromosome: CHR5: 171760502-171881527
Locus: 5q35.1
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: FTHS FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SH3PXD2B-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping