KIF5B-HPS4 Fusion FISH Probe
The KIF5B-HPS4 Fusion FISH Probe is used to confirm a fusion of the KIF5B and HPS4 genes. The fusion of the KIF5B and HPS4 genes has been associated with Breast Invasive Carcinoma. 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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KIF5B-HPS4-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-RERE | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-REOR | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-REGO | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-REGR | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-REAQ | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-ORRE | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-OROR | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-ORGO | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-ORAQ | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-GORE | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-GOOR | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-GOGO | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-GOGR | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-GOAQ | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-GRRE | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-GROR | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-GRGO | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-GRGR | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-GRAQ | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-AQRE | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-AQOR | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-AQGO | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-AQGR | 20 (40 μL) | 200 μL | ||
KIF5B-HPS4-20-AQAQ | 20 (40 μL) | 200 μL |
KIF5B Gene Summary
The Kinesin Family Member 5B (KIF5B) gene is located on chr10 :32297937-32345371 at 10p11.22.
Gene Name: Kinesin Family Member 5B
Chromosome: CHR10: 32297937 -32345371
Locus: 10p11.22
HPS4 Gene Summary
This gene encodes a protein component of biogenesis of lysosome-related organelles complexes (BLOC). BLOC complexes are important for the formation of endosomal-lysosomal organelles such as melanosomes and platelet dense granules. Mutations in this gene result in subtype 4 of Hermansky-Pudlak syndrome, a form of albinism. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]
Gene Name: HPS4, Biogenesis Of Lysosomal Organelles Complex 3 Subunit 2
Chromosome: CHR22: 26847445 -26879820
Locus: 22q12.1
Gene Diseases
The KIF5B HPS4 Fusion has been associated with the following diseases:
Disease Name |
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Breast Invasive Carcinoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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