STXBP5L Break Apart FISH Probe
Empire Genomics’ STXBP5L Break Apart FISH Probe is designed to flank the STXBP5L gene and is typically used for detecting STXBP5L 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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STXBP5LBA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
STXBP5LBA-20-AQOR | 20 (40 μL) | 200 μL | ||
STXBP5LBA-20-GOGR | 20 (40 μL) | 200 μL | ||
STXBP5LBA-20-GORE | 20 (40 μL) | 200 μL | ||
STXBP5LBA-20-GRGO | 20 (40 μL) | 200 μL | ||
STXBP5LBA-20-GROR | 20 (40 μL) | 200 μL | ||
STXBP5LBA-20-GRRE | 20 (40 μL) | 200 μL | ||
STXBP5LBA-20-REGO | 20 (40 μL) | 200 μL | ||
STXBP5LBA-20-REGR | 20 (40 μL) | 200 μL |
Gene Summary
The protein encoded by this gene is similar to syntaxin-binding protein 5 and contains ten N-terminal WD40 repeats, four variable region WD40 repeats, and a C-terminal R-SNARE domain. Studies of the orthologous proteins in mouse and rat have shown that the encoded protein may inhibit exocytosis in neurosecretory cells, and may negatively regulate the secretion of insulin. A missense variant in this gene is likely the cause of an infantile-onset neurodegenerative disorder diagnosed in two siblings of consanguineous parents. [provided by RefSeq, Jan 2017]
Gene Details
Gene Symbol: STXBP5L
Gene Name: Syntaxin Binding Protein 5 Like
Chromosome: CHR3: 120627049-121143608
Locus: 3q13.33
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: STXBP5L FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: STXBP5L-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping