SCMH1-PPT1 Fusion FISH Probe
The SCMH1-PPT1 Fusion FISH Probe is used to confirm a fusion of the SCMH1 and PPT1 genes. The fusion of the SCMH1 and PPT1 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. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.
SKU | Test Kits | Buffer | Dye Color | Order Now |
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SCMH1-PPT1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-RERE | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-REOR | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-REGO | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-REGR | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-REAQ | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-ORRE | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-OROR | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-ORGO | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-ORAQ | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-GORE | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-GOOR | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-GOGO | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-GOGR | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-GOAQ | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-GRRE | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-GROR | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-GRGO | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-GRGR | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-GRAQ | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-AQRE | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-AQOR | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-AQGO | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-AQGR | 20 (40 μL) | 200 μL | ||
SCMH1-PPT1-20-AQAQ | 20 (40 μL) | 200 μL |
PPT1 Gene Summary
The protein encoded by this gene is a small glycoprotein involved in the catabolism of lipid-modified proteins during lysosomal degradation. The encoded enzyme removes thioester-linked fatty acyl groups such as palmitate from cysteine residues. Defects in this gene are a cause of infantile neuronal ceroid lipofuscinosis 1 (CLN1, or INCL) and neuronal ceroid lipofuscinosis 4 (CLN4). Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Dec 2008]
Gene Name: Palmitoyl-protein Thioesterase 1
Chromosome: CHR1: 40538381 -40563142
Locus: 1p34.2
SCMH1 Gene Summary
The Scm Polycomb Group Protein Homolog 1 (SCMH1) gene is located on chr1 :41492870-41707815 at 1p34.2.
Gene Name: Scm Polycomb Group Protein Homolog 1
Chromosome: CHR1: 41492870 -41707815
Locus: 1p34.2
Gene Diseases
The SCMH1 PPT1 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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