TSHZ1-RNASEH2B Fusion FISH Probe
The TSHZ1-RNASEH2B Fusion FISH Probe is used to confirm a fusion of the TSHZ1 and RNASEH2B genes. The fusion of the TSHZ1 and RNASEH2B genes has been associated with Sarcoma. 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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| TSHZ1-RNASEH2B-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-RERE | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-REOR | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-REGO | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-REGR | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-REAQ | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-ORRE | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-OROR | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-ORGO | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-ORAQ | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-GORE | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-GOOR | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-GOGO | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-GOGR | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-GOAQ | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-GRRE | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-GROR | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-GRGO | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-GRGR | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-GRAQ | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-AQRE | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-AQOR | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-AQGO | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-AQGR | 20 (40 μL) | 200 μL |
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| TSHZ1-RNASEH2B-20-AQAQ | 20 (40 μL) | 200 μL |
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TSHZ1 Gene Summary
This gene encodes a colon cancer antigen that was defined by serological analysis of recombinant cDNA expression libraries. The encoded protein is a member of the teashirt C2H2-type zinc-finger protein family and may be involved in transcriptional regulation of developmental processes. Mutations in this gene may be associated with congenital aural atresia syndrome. [provided by RefSeq, Jan 2012]
Gene Name: Teashirt Zinc Finger Homeobox 1
Chromosome: CHR18: 72922730 -73001901
Locus: 18q22.3
RNASEH2B Gene Summary
RNase H2 is composed of a single catalytic subunit (A) and two non-catalytic subunits (B and C) and specifically degrades the RNA of RNA:DNA hybrids. The protein encoded by this gene is the non-catalytic B subunit of RNase H2, which is thought to play a role in DNA replication. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Aicardi-Goutieres syndrome type 2 (AGS2). [provided by RefSeq, Nov 2008]
Gene Name: Ribonuclease H2 Subunit B
Chromosome: CHR13: 51483813 -51544596
Locus: 13q14.3
Gene Diseases
The TSHZ1 RNASEH2B Fusion has been associated with the following diseases:
| Disease Name |
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| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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