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LAMA2-SLC11A2 Fusion FISH Probe

The LAMA2-SLC11A2 Fusion FISH Probe is used to confirm a fusion of the LAMA2 and SLC11A2 genes. The fusion of the LAMA2 and SLC11A2 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.

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

SKU Test Kits Buffer Dye Color Order Now
LAMA2-SLC11A2-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-RERE 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-REOR 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-REGO 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-REGR 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-REAQ 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-ORRE 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-OROR 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-ORGO 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-ORAQ 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-GORE 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-GOOR 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-GOGO 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-GOGR 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-GOAQ 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-GRRE 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-GROR 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-GRGO 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-GRGR 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-GRAQ 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-AQRE 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-AQOR 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-AQGO 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-AQGR 20 (40 μL) 200 μL
LAMA2-SLC11A2-20-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

SLC11A2 Gene Summary

This gene encodes a member of the solute carrier family 11 protein family. The product of this gene transports divalent metals and is involved in iron absorption. Mutations in this gene are associated with hypochromic microcytic anemia with iron overload. A related solute carrier family 11 protein gene is located on chromosome 2. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Apr 2010]

Gene Name: Solute Carrier Family 11 Member 2

Chromosome: CHR12: 51373565 -51420199

Locus: 12q13.12

Gene Diseases

The LAMA2 SLC11A2 Fusion has been associated with the following diseases:

Disease Name
Sarcoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.