BHLHA9 FISH Probe
The BHLHA9 FISH probe is designed to hybridize to the BHLHA9 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 |
|---|---|---|---|---|
| BHLHA9-20-OR (Standard Design) | 20 (40 μL) | 200 μL |  |
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| BHLHA9-20-RE | 20 (40 μL) | 200 μL |  |
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| BHLHA9-20-GO | 20 (40 μL) | 200 μL |  |
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| BHLHA9-20-GR | 20 (40 μL) | 200 μL |  |
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| BHLHA9-20-AQ | 20 (40 μL) | 200 μL |  |
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| BHLHA9-20-DIG | 20 (40 μL) | 200 μL |  |
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| BHLHA9-20-BIO | 20 (40 μL) | 200 μL |  |
Gene Summary
This gene is a member of the basic helix-loop-helix family. The encoded protein is a transcription factor involved in limb development. Mutations in this gene have been associated with mesoaxial synostotic syndactyly Malik-Percin type (MSSD). Copy number variation of a locus containing this gene has been linked to a form of split-hand/foot malformation with long bone deficiency (SHFLD3). [provided by RefSeq, Mar 2015]
Gene Details
Gene Symbol: BHLHA9
Gene Name: Basic Helix-loop-helix Family Member A9
Chromosome: CHR17: 1173857-1174565
Locus: 17p13.3
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: BHLHA9 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: BHLHA9-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping