NFASC-PPP1R12B Fusion FISH Probe
The NFASC-PPP1R12B Fusion FISH Probe is used to confirm a fusion of the NFASC and PPP1R12B genes. The fusion of the NFASC and PPP1R12B genes has been associated with Brain Lower Grade Glioma. 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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| NFASC-PPP1R12B-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-RERE | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-REOR | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-REGO | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-REGR | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-REAQ | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-ORRE | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-OROR | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-ORGO | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-ORAQ | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-GORE | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-GOOR | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-GOGO | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-GOGR | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-GOAQ | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-GRRE | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-GROR | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-GRGO | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-GRGR | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-GRAQ | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-AQRE | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-AQOR | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-AQGO | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-AQGR | 20 (40 μL) | 200 μL |
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| NFASC-PPP1R12B-20-AQAQ | 20 (40 μL) | 200 μL |
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PPP1R12B Gene Summary
Myosin phosphatase is a protein complex comprised of three subunits: a catalytic subunit (PP1c-delta, protein phosphatase 1, catalytic subunit delta), a large regulatory subunit (MYPT, myosin phosphatase target) and small regulatory subunit (sm-M20). Two isoforms of MYPT have been isolated--MYPT1 and MYPT2, the first of which is widely expressed, and the second of which may be specific to heart, skeletal muscle, and brain. Each of the MYPT isoforms functions to bind PP1c-delta and increase phosphatase activity. This locus encodes both MYTP2 and M20. Alternatively spliced transcript variants encoding different isoforms have been identified. Related pseudogenes have been defined on the Y chromosome. [provided by RefSeq, Oct 2011]
Gene Name: Protein Phosphatase 1 Regulatory Subunit 12B
Chromosome: CHR1: 202317829 -202557697
Locus: 1q32.1
NFASC Gene Summary
This gene encodes an L1 family immunoglobulin cell adhesion molecule with multiple IGcam and fibronectin domains. The protein functions in neurite outgrowth, neurite fasciculation, and organization of the axon initial segment (AIS) and nodes of Ranvier on axons during early development. Both the AIS and nodes of Ranvier contain high densities of voltage-gated Na+ (Nav) channels which are clustered by interactions with cytoskeletal and scaffolding proteins including this protein, gliomedin, ankyrin 3 (ankyrin-G), and betaIV spectrin. This protein links the AIS extracellular matrix to the intracellular cytoskeleton. This gene undergoes extensive alternative splicing, and the full-length nature of some variants has not been determined.[provided by RefSeq, May 2009]
Gene Name: Neurofascin
Chromosome: CHR1: 204797781 -204991950
Locus: 1q32.1
Gene Diseases
The NFASC PPP1R12B Fusion has been associated with the following diseases:
| Disease Name |
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| Brain Lower Grade Glioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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