RAP1GAP-NSDHL Fusion FISH Probe
The RAP1GAP-NSDHL Fusion FISH Probe is used to confirm a fusion of the RAP1GAP and NSDHL genes. The fusion of the RAP1GAP and NSDHL 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| RAP1GAP-NSDHL-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-RERE | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-REOR | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-REGO | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-REGR | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-REAQ | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-ORRE | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-OROR | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-ORGO | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-ORAQ | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-GORE | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-GOOR | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-GOGO | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-GOGR | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-GOAQ | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-GRRE | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-GROR | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-GRGO | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-GRGR | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-GRAQ | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-AQRE | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-AQOR | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-AQGO | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-AQGR | 20 (40 μL) | 200 μL |
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| RAP1GAP-NSDHL-20-AQAQ | 20 (40 μL) | 200 μL |
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RAP1GAP Gene Summary
This gene encodes a type of GTPase-activating-protein (GAP) that down-regulates the activity of the ras-related RAP1 protein. RAP1 acts as a molecular switch by cycling between an inactive GDP-bound form and an active GTP-bound form. The product of this gene, RAP1GAP, promotes the hydrolysis of bound GTP and hence returns RAP1 to the inactive state whereas other proteins, guanine nucleotide exchange factors (GEFs), act as RAP1 activators by facilitating the conversion of RAP1 from the GDP- to the GTP-bound form. In general, ras subfamily proteins, such as RAP1, play key roles in receptor-linked signaling pathways that control cell growth and differentiation. RAP1 plays a role in diverse processes such as cell proliferation, adhesion, differentiation, and embryogenesis. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Aug 2011]
Gene Name: RAP1 GTPase Activating Protein
Chromosome: CHR1: 21922707 -21995856
Locus: 1p36.12
NSDHL Gene Summary
The protein encoded by this gene is localized in the endoplasmic reticulum and is involved in cholesterol biosynthesis. Mutations in this gene are associated with CHILD syndrome, which is a X-linked dominant disorder of lipid metabolism with disturbed cholesterol biosynthesis, and typically lethal in males. Alternatively spliced transcript variants with differing 5' UTR have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Name: NAD(P) Dependent Steroid Dehydrogenase-like
Chromosome: CHRX: 151999510 -152037907
Locus: Xq28
Gene Diseases
The RAP1GAP NSDHL 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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