PRSS12 Break Apart FISH Probe
Empire Genomics’ PRSS12 Break Apart FISH Probe is designed to flank the PRSS12 gene and is typically used for detecting PRSS12 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 |
---|---|---|---|---|
PRSS12BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL | ||
PRSS12BA-20-AQOR | 20 (40 μL) | 200 μL | ||
PRSS12BA-20-GOGR | 20 (40 μL) | 200 μL | ||
PRSS12BA-20-GORE | 20 (40 μL) | 200 μL | ||
PRSS12BA-20-GRGO | 20 (40 μL) | 200 μL | ||
PRSS12BA-20-GRRE | 20 (40 μL) | 200 μL | ||
PRSS12BA-20-ORGR | 20 (40 μL) | 200 μL | ||
PRSS12BA-20-REGO | 20 (40 μL) | 200 μL | ||
PRSS12BA-20-REGR | 20 (40 μL) | 200 μL |
Gene Summary
This gene encodes a member of the trypsin family of serine proteases and contains a signal peptide, a proline-rich region, a Kringle domain, four scavenger receptor cysteine-rich domains, and a trypsin-like serine protease domain. The protein, sometimes referred to as neurotrypsin or motopsin, is secreted from neuronal cells and localizes to the synaptic cleft. Studies in mice show that this protein cleaves a protein, agrin, that is important for the formation and maintenance of exitatory synapses. Defects in this gene cause a form of autosomal recessive cognitive impairment (MRT1). [provided by RefSeq, Jul 2017]
Gene Details
Gene Symbol: PRSS12
Gene Name: Protease, Serine 12
Chromosome: CHR4: 119201192-119273922
Locus: 4q26
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: PRSS12 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: PRSS12-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping