HOXB13 Break Apart FISH Probe
Empire Genomics’ HOXB13 Break Apart FISH Probe is designed to flank the HOXB13 gene and is typically used for detecting HOXB13 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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| HOXB13BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| HOXB13BA-20-AQOR | 20 (40 μL) | 200 μL |
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| HOXB13BA-20-GOGR | 20 (40 μL) | 200 μL |
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| HOXB13BA-20-GORE | 20 (40 μL) | 200 μL |
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| HOXB13BA-20-GRGO | 20 (40 μL) | 200 μL |
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| HOXB13BA-20-GRRE | 20 (40 μL) | 200 μL |
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| HOXB13BA-20-ORGR | 20 (40 μL) | 200 μL |
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| HOXB13BA-20-REGO | 20 (40 μL) | 200 μL |
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| HOXB13BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This gene encodes a transcription factor that belongs to the homeobox gene family. Genes of this family are highly conserved among vertebrates and essential for vertebrate embryonic development. This gene has been implicated to play a role in fetal skin development and cutaneous regeneration. In mice, a similar gene was shown to exhibit temporal and spatial colinearity in the main body axis of the embryo, but was not expressed in the secondary axes, which suggests functions in body patterning along the axis. This gene and other HOXB genes form a gene cluster at chromosome the 17q21-22 region. [provided by RefSeq, Jul 2008]
Gene Details
Gene Symbol: HOXB13
Gene Name: Homeobox B13
Chromosome: CHR17: 46802126-46806111
Locus: 17q21.32
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: HOXB13 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: HOXB13-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping