FRA16A Break Apart FISH Probe
Empire Genomics’ FRA16A Break Apart FISH Probe is designed to flank the FRA16A gene and is typically used for detecting FRA16A 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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FRA16ABA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL | ||
FRA16ABA-20-AQOR | 20 (40 μL) | 200 μL | ||
FRA16ABA-20-GOGR | 20 (40 μL) | 200 μL | ||
FRA16ABA-20-GORE | 20 (40 μL) | 200 μL | ||
FRA16ABA-20-GRGO | 20 (40 μL) | 200 μL | ||
FRA16ABA-20-GRRE | 20 (40 μL) | 200 μL | ||
FRA16ABA-20-ORGR | 20 (40 μL) | 200 μL | ||
FRA16ABA-20-REGO | 20 (40 μL) | 200 μL | ||
FRA16ABA-20-REGR | 20 (40 μL) | 200 μL |
Gene Summary
There are several phenotypes associated with variation in pericentric region of chromosome 16: see the 16p12.2-p11.2 deletion syndrome (MIM 613604); see MIM 611913 for a deletion or duplication at 16p11.2 associated with autism (AUTS14); and see MIM 613444 for a 220-kb deletion at 16p11.2 associated with isolated severe early-onset obesity and obesity with developmental delay.[supplied by OMIM, Nov 2010]
Gene Details
Gene Symbol: FRA16A
Gene Name: Fragile Site, Folic Acid Type, Rare, Fra(16)(p13.11)
Locus: 16p13.11
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: FRA16A FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: FRA16A-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping