SNX14-SYNCRIP Fusion FISH Probe
The SNX14-SYNCRIP Fusion FISH Probe is used to confirm a fusion of the SNX14 and SYNCRIP genes. The fusion of the SNX14 and SYNCRIP genes has been associated with Head And Neck Squamous Cell Carcinoma . These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.
** This product is for in vitro and research use only. This product is not intended for diagnostic use. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| SNX14-SYNCRIP-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-RERE | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-REOR | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-REGO | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-REGR | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-REAQ | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-ORRE | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-OROR | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-ORGO | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-ORAQ | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-GORE | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-GOOR | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-GOGO | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-GOGR | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-GOAQ | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-GRRE | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-GROR | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-GRGO | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-GRGR | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-GRAQ | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-AQRE | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-AQOR | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-AQGO | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-AQGR | 20 (40 μL) | 200 μL |
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| SNX14-SYNCRIP-20-AQAQ | 20 (40 μL) | 200 μL |
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SYNCRIP Gene Summary
This gene encodes a member of the cellular heterogeneous nuclear ribonucleoprotein (hnRNP) family. hnRNPs are RNA binding proteins that complex with heterogeneous nuclear RNA (hnRNA) and regulate alternative splicing, polyadenylation, and other aspects of mRNA metabolism and transport. The encoded protein plays a role in multiple aspects of mRNA maturation and is associated with several multiprotein complexes including the apoB RNA editing-complex and survival of motor neurons (SMN) complex. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the short arm of chromosome 20. [provided by RefSeq, Dec 2011]
Gene Name: Synaptotagmin Binding Cytoplasmic RNA Interacting Protein
Chromosome: CHR6: 86317501 -86353043
Locus: 6q14.3
SNX14 Gene Summary
This gene encodes a member of the sorting nexin family. Members of this family have a phox (PX) phosphoinositide binding domain and are involved in intracellular trafficking. The encoded protein also contains a regulator of G protein signaling (RGS) domain. Regulator of G protein signaling family members are regulatory molecules that act as GTPase activating proteins for G alpha subunits of heterotrimeric G proteins. Alternate splicing results in transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2014]
Gene Name: Sorting Nexin 14
Chromosome: CHR6: 86215214 -86303629
Locus: 6q14.3
Gene Diseases
The SNX14 SYNCRIP Fusion has been associated with the following diseases:
| Disease Name |
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| Head And Neck Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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