FOXD4L1 Break Apart FISH Probe
Empire Genomics’ FOXD4L1 Break Apart FISH Probe is designed to flank the FOXD4L1 gene and is typically used for detecting FOXD4L1 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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FOXD4L1BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
FOXD4L1BA-20-AQOR | 20 (40 μL) | 200 μL | ||
FOXD4L1BA-20-GOGR | 20 (40 μL) | 200 μL | ||
FOXD4L1BA-20-GORE | 20 (40 μL) | 200 μL | ||
FOXD4L1BA-20-GRGO | 20 (40 μL) | 200 μL | ||
FOXD4L1BA-20-GROR | 20 (40 μL) | 200 μL | ||
FOXD4L1BA-20-GRRE | 20 (40 μL) | 200 μL | ||
FOXD4L1BA-20-REGO | 20 (40 μL) | 200 μL | ||
FOXD4L1BA-20-REGR | 20 (40 μL) | 200 μL |
Gene Summary
This gene is a member of the forkhead/winged-helix (FOX) family of transcription factors with highly conserved FOX DNA-binding domains. Members of the FOX family of transcription factors are regulators of embryogenesis and may play a role in human cancer. This gene lies in a region of chromosome 2 that surrounds the site where two ancestral chromosomes fused to form human chromosome 2. This region is duplicated elsewhere in the human genome, primarily in subtelomeric and pericentromeric locations, thus mutiple copies of this gene have been found. [provided by RefSeq, Jul 2008]
Gene Details
Gene Symbol: FOXD4L1
Gene Name: Forkhead Box D4 Like 1
Chromosome: CHR2: 114256660-114258727
Locus: 2q14.1
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: FOXD4L1 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: FOXD4L1-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping