NSFL1C Break Apart FISH Probe
Empire Genomics’ NSFL1C Break Apart FISH Probe is designed to flank the NSFL1C gene and is typically used for detecting NSFL1C 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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| NSFL1CBA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| NSFL1CBA-20-AQOR | 20 (40 μL) | 200 μL |
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| NSFL1CBA-20-GOGR | 20 (40 μL) | 200 μL |
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| NSFL1CBA-20-GORE | 20 (40 μL) | 200 μL |
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| NSFL1CBA-20-GRGO | 20 (40 μL) | 200 μL |
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| NSFL1CBA-20-GRRE | 20 (40 μL) | 200 μL |
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| NSFL1CBA-20-ORGR | 20 (40 μL) | 200 μL |
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| NSFL1CBA-20-REGO | 20 (40 μL) | 200 μL |
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| NSFL1CBA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
N-ethylmaleimide-sensitive factor (NSF) and valosin-containing protein (p97) are two ATPases known to be involved in transport vesicle/target membrane fusion and fusions between membrane compartments. A trimer of the protein encoded by this gene binds a hexamer of cytosolic p97 and is required for p97-mediated regrowth of Golgi cisternae from mitotic Golgi fragments. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 8. [provided by RefSeq, May 2011]
Gene Details
Gene Symbol: NSFL1C
Gene Name: NSFL1 Cofactor
Chromosome: CHR20: 1422806-1448337
Locus: 20p13
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: NSFL1C FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: NSFL1C-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping