SH3PXD2B Break Apart FISH Probe
Empire Genomics’ SH3PXD2B Break Apart FISH Probe is designed to flank the SH3PXD2B gene and is typically used for detecting SH3PXD2B rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in green and orange by default, but may be customized to meet your needs.
** 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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| SH3PXD2BBA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| SH3PXD2BBA-20-AQOR | 20 (40 μL) | 200 μL |
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| SH3PXD2BBA-20-GOGR | 20 (40 μL) | 200 μL |
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| SH3PXD2BBA-20-GORE | 20 (40 μL) | 200 μL |
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| SH3PXD2BBA-20-GRGO | 20 (40 μL) | 200 μL |
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| SH3PXD2BBA-20-GRRE | 20 (40 μL) | 200 μL |
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| SH3PXD2BBA-20-ORGR | 20 (40 μL) | 200 μL |
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| SH3PXD2BBA-20-REGO | 20 (40 μL) | 200 μL |
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| SH3PXD2BBA-20-REGR | 20 (40 μL) | 200 μL |
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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: SH3PXD2B 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