IFT122-PITPNB Fusion FISH Probe
The IFT122-PITPNB Fusion FISH Probe is used to confirm a fusion of the IFT122 and PITPNB genes. The fusion of the IFT122 and PITPNB genes has been associated with Prostate Adenocarcinoma. 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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| IFT122-PITPNB-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-RERE | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-REOR | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-REGO | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-REGR | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-REAQ | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-ORRE | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-OROR | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-ORGO | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-ORAQ | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-GORE | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-GOOR | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-GOGO | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-GOGR | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-GOAQ | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-GRRE | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-GROR | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-GRGO | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-GRGR | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-GRAQ | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-AQRE | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-AQOR | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-AQGO | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-AQGR | 20 (40 μL) | 200 μL |
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| IFT122-PITPNB-20-AQAQ | 20 (40 μL) | 200 μL |
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PITPNB Gene Summary
This gene encodes a cytoplasmic protein that catalyzes the transfer of phosphatidylinositol and phosphatidylcholine between membranes. This transfer activity is required for COPI complex-mediated retrograde transport from the Golgi apparatus to the endoplasmic reticulum. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Sep 2013]
Gene Name: Phosphatidylinositol Transfer Protein Beta
Chromosome: CHR22: 28247656 -28315255
Locus: 22q12.1
IFT122 Gene Summary
This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This cytoplasmic protein contains seven WD repeats and an AF-2 domain which function by recruiting coregulatory molecules and in transcriptional activation. Mutations in this gene cause cranioectodermal dysplasia-1. A related pseudogene is located on chromosome 3. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]
Gene Name: Intraflagellar Transport 122
Chromosome: CHR3: 129158967 -129239191
Locus: 3q21.3-q22.1
Gene Diseases
The IFT122 PITPNB Fusion has been associated with the following diseases:
| Disease Name |
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| Prostate Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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