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MYH9-CACNA1C Fusion FISH Probe

The MYH9-CACNA1C Fusion FISH Probe is used to confirm a fusion of the MYH9 and CACNA1C genes. The fusion of the MYH9 and CACNA1C genes has been associated with Acute Myeloid Leukemia. 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.

Turnaround Time: 7-10 Business Days    Shipping Time: 1-2 Day Expedited Shipping

SKU Test Kits Buffer Dye Color Order Now
MYH9-CACNA1C-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
MYH9-CACNA1C-20-RERE 20 (40 μL) 200 μL
MYH9-CACNA1C-20-REOR 20 (40 μL) 200 μL
MYH9-CACNA1C-20-REGO 20 (40 μL) 200 μL
MYH9-CACNA1C-20-REGR 20 (40 μL) 200 μL
MYH9-CACNA1C-20-REAQ 20 (40 μL) 200 μL
MYH9-CACNA1C-20-ORRE 20 (40 μL) 200 μL
MYH9-CACNA1C-20-OROR 20 (40 μL) 200 μL
MYH9-CACNA1C-20-ORGO 20 (40 μL) 200 μL
MYH9-CACNA1C-20-ORAQ 20 (40 μL) 200 μL
MYH9-CACNA1C-20-GORE 20 (40 μL) 200 μL
MYH9-CACNA1C-20-GOOR 20 (40 μL) 200 μL
MYH9-CACNA1C-20-GOGO 20 (40 μL) 200 μL
MYH9-CACNA1C-20-GOGR 20 (40 μL) 200 μL
MYH9-CACNA1C-20-GOAQ 20 (40 μL) 200 μL
MYH9-CACNA1C-20-GRRE 20 (40 μL) 200 μL
MYH9-CACNA1C-20-GROR 20 (40 μL) 200 μL
MYH9-CACNA1C-20-GRGO 20 (40 μL) 200 μL
MYH9-CACNA1C-20-GRGR 20 (40 μL) 200 μL
MYH9-CACNA1C-20-GRAQ 20 (40 μL) 200 μL
MYH9-CACNA1C-20-AQRE 20 (40 μL) 200 μL
MYH9-CACNA1C-20-AQOR 20 (40 μL) 200 μL
MYH9-CACNA1C-20-AQGO 20 (40 μL) 200 μL
MYH9-CACNA1C-20-AQGR 20 (40 μL) 200 μL
MYH9-CACNA1C-20-AQAQ 20 (40 μL) 200 μL

CACNA1C Gene Summary

This gene encodes an alpha-1 subunit of a voltage-dependent calcium channel. Calcium channels mediate the influx of calcium ions into the cell upon membrane polarization. The alpha-1 subunit consists of 24 transmembrane segments and forms the pore through which ions pass into the cell. The calcium channel consists of a complex of alpha-1, alpha-2/delta, beta, and gamma subunits in a 1:1:1:1 ratio. There are multiple isoforms of each of these proteins, either encoded by different genes or the result of alternative splicing of transcripts. The protein encoded by this gene binds to and is inhibited by dihydropyridine. Alternative splicing results in many transcript variants encoding different proteins. Some of the predicted proteins may not produce functional ion channel subunits. [provided by RefSeq, Oct 2012]

Gene Name: Calcium Voltage-gated Channel Subunit Alpha1 C

Chromosome: CHR12: 2162415 -2807115

Locus: 12p13.33

MYH9 Gene Summary

This gene encodes a conventional non-muscle myosin; this protein should not be confused with the unconventional myosin-9a or 9b (MYO9A or MYO9B). The encoded protein is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain which is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in this gene have been associated with non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness. [provided by RefSeq, Dec 2011]

Gene Name: Myosin Heavy Chain 9

Chromosome: CHR22: 36677322 -36784063

Locus: 22q12.3

Gene Diseases

The MYH9 CACNA1C Fusion has been associated with the following diseases:

Disease Name
Acute Myeloid Leukemia

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.