FAM129B-SNRNP25 Fusion FISH Probe
The FAM129B-SNRNP25 Fusion FISH Probe is used to confirm a fusion of the FAM129B and SNRNP25 genes. The fusion of the FAM129B and SNRNP25 genes has been associated with Skin Cutaneous Melanoma. 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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FAM129B-SNRNP25-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-RERE | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-REOR | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-REGO | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-REGR | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-REAQ | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-ORRE | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-OROR | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-ORGO | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-ORAQ | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-GORE | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-GOOR | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-GOGO | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-GOGR | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-GOAQ | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-GRRE | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-GROR | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-GRGO | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-GRGR | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-GRAQ | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-AQRE | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-AQOR | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-AQGO | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-AQGR | 20 (40 μL) | 200 μL | ||
FAM129B-SNRNP25-20-AQAQ | 20 (40 μL) | 200 μL |
FAM129B Gene Summary
The Family With Sequence Similarity 129 Member B (FAM129B) gene is located on chr9 :130267617-130341268 at 9q34.11.
Gene Name: Family With Sequence Similarity 129 Member B
Chromosome: CHR9: 130267617 -130341268
Locus: 9q34.11
SNRNP25 Gene Summary
Two types of spliceosomes catalyze splicing of pre-mRNAs. The major U2-type spliceosome is found in all eukaryotes and removes U2-type introns, which represent more than 99% of pre-mRNA introns. The minor U12-type spliceosome is found in some eukaryotes and removes U12-type introns, which are rare and have distinct splice consensus signals. The U12-type spliceosome consists of several small nuclear RNAs and associated proteins. This gene encodes a 25K protein that is a component of the U12-type spliceosome. [provided by RefSeq, Apr 2010]
Gene Name: Small Nuclear Ribonucleoprotein U11/U12 Subunit 25
Chromosome: CHR16: 103828 -107669
Locus: 16p13.3
Gene Diseases
The FAM129B SNRNP25 Fusion has been associated with the following diseases:
Disease Name |
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Skin Cutaneous Melanoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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