HNF1A Break Apart FISH Probe
Empire Genomics’ HNF1A Break Apart FISH Probe is designed to flank the HNF1A gene and is typically used for detecting HNF1A 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 |
|---|---|---|---|---|
| HNF1ABA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| HNF1ABA-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| HNF1ABA-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| HNF1ABA-20-GORE | 20 (40 μL) | 200 μL |
|
|
| HNF1ABA-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| HNF1ABA-20-GROR | 20 (40 μL) | 200 μL |
|
|
| HNF1ABA-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| HNF1ABA-20-REGO | 20 (40 μL) | 200 μL |
|
|
| HNF1ABA-20-REGR | 20 (40 μL) | 200 μL |
|
Gene Summary
The protein encoded by this gene is a transcription factor required for the expression of several liver-specific genes. The encoded protein functions as a homodimer and binds to the inverted palindrome 5'-GTTAATNATTAAC-3'. Defects in this gene are a cause of maturity onset diabetes of the young type 3 (MODY3) and also can result in the appearance of hepatic adenomas. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2015]
Gene Details
Gene Symbol: HNF1A
Gene Name: HNF1 Homeobox A
Chromosome: CHR12: 121416548-121440314
Locus: 12q24.31
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|
Customer Publications
Product Details
Product: HNF1A FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: HNF1A-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping