NHSL1-LAMA2 Fusion FISH Probe
The NHSL1-LAMA2 Fusion FISH Probe is used to confirm a fusion of the NHSL1 and LAMA2 genes. The fusion of the NHSL1 and LAMA2 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. 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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NHSL1-LAMA2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-RERE | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-REOR | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-REGO | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-REGR | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-REAQ | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-ORRE | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-OROR | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-ORGO | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-ORAQ | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-GORE | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-GOOR | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-GOGO | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-GOGR | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-GOAQ | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-GRRE | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-GROR | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-GRGO | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-GRGR | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-GRAQ | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-AQRE | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-AQOR | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-AQGO | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-AQGR | 20 (40 μL) | 200 μL | ||
NHSL1-LAMA2-20-AQAQ | 20 (40 μL) | 200 μL |
LAMA2 Gene Summary
Laminin, an extracellular protein, is a major component of the basement membrane. It is thought to mediate the attachment, migration, and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components. It is composed of three subunits, alpha, beta, and gamma, which are bound to each other by disulfide bonds into a cross-shaped molecule. This gene encodes the alpha 2 chain, which constitutes one of the subunits of laminin 2 (merosin) and laminin 4 (s-merosin). Mutations in this gene have been identified as the cause of congenital merosin-deficient muscular dystrophy. Two transcript variants encoding different proteins have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Name: Laminin Subunit Alpha 2
Chromosome: CHR6: 129204285 -129837710
Locus: 6q22.33
NHSL1 Gene Summary
The NHS Like 1 (NHSL1) gene is located on chr6 :138743180-138893668 at 6q24.1.
Gene Name: NHS Like 1
Chromosome: CHR6: 138743180 -138893668
Locus: 6q24.1
Gene Diseases
The NHSL1 LAMA2 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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