BHLHA9 Break Apart FISH Probe
Empire Genomics’ BHLHA9 Break Apart FISH Probe is designed to flank the BHLHA9 gene and is typically used for detecting BHLHA9 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in orange and green 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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| BHLHA9BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| BHLHA9BA-20-AQOR | 20 (40 μL) | 200 μL |
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| BHLHA9BA-20-GOGR | 20 (40 μL) | 200 μL |
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| BHLHA9BA-20-GORE | 20 (40 μL) | 200 μL |
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| BHLHA9BA-20-GRGO | 20 (40 μL) | 200 μL |
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| BHLHA9BA-20-GROR | 20 (40 μL) | 200 μL |
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| BHLHA9BA-20-GRRE | 20 (40 μL) | 200 μL |
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| BHLHA9BA-20-REGO | 20 (40 μL) | 200 μL |
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| BHLHA9BA-20-REGR | 20 (40 μL) | 200 μL |
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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