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SLC35A1-LRRFIP1 Fusion FISH Probe

The SLC35A1-LRRFIP1 Fusion FISH Probe is used to confirm a fusion of the SLC35A1 and LRRFIP1 genes. The fusion of the SLC35A1 and LRRFIP1 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
SLC35A1-LRRFIP1-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-RERE 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-REOR 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-REGO 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-REGR 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-REAQ 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-ORRE 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-OROR 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-ORGO 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-ORAQ 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-GORE 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-GOOR 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-GOGO 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-GOGR 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-GOAQ 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-GRRE 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-GROR 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-GRGO 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-GRGR 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-GRAQ 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-AQRE 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-AQOR 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-AQGO 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-AQGR 20 (40 μL) 200 μL
SLC35A1-LRRFIP1-20-AQAQ 20 (40 μL) 200 μL

LRRFIP1 Gene Summary

The LRR Binding FLII Interacting Protein 1 (LRRFIP1) gene is located on chr2 :238536223-238690290 at 2q37.3.

Gene Name: LRR Binding FLII Interacting Protein 1

Chromosome: CHR2: 238536223 -238690290

Locus: 2q37.3

SLC35A1 Gene Summary

The protein encoded by this gene is found in the membrane of the Golgi apparatus, where it transports nucleotide sugars into the Golgi. One such nucleotide sugar is CMP-sialic acid, which is imported into the Golgi by the encoded protein and subsequently glycosylated. Defects in this gene are a cause of congenital disorder of glycosylation type 2F (CDG2F). Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Dec 2009]

Gene Name: Solute Carrier Family 35 Member A1

Chromosome: CHR6: 88182642 -88222057

Locus: 6q15

Gene Diseases

The SLC35A1 LRRFIP1 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.