SEARCH OUR PRODUCT CATALOG

C11ORF48-BSCL2 Fusion FISH Probe

The C11ORF48-BSCL2 Fusion FISH Probe is used to confirm a fusion of the C11ORF48 and BSCL2 genes. The fusion of the C11ORF48 and BSCL2 genes has been associated with Brain Lower Grade Glioma. 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.

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

SKU Test Kits Buffer Dye Color Order Now
C11ORF48-BSCL2-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-RERE 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-REOR 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-REGO 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-REGR 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-REAQ 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-ORRE 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-OROR 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-ORGO 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-ORAQ 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-GORE 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-GOOR 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-GOGO 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-GOGR 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-GOAQ 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-GRRE 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-GROR 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-GRGO 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-GRGR 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-GRAQ 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-AQRE 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-AQOR 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-AQGO 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-AQGR 20 (40 μL) 200 μL
C11ORF48-BSCL2-20-AQAQ 20 (40 μL) 200 μL

BSCL2 Gene Summary

This gene encodes the multi-pass transmembrane protein protein seipin. This protein localizes to the endoplasmic reticulum and may be important for lipid droplet morphology. Mutations in this gene have been associated with congenital generalized lipodystrophy type 2 or Berardinelli-Seip syndrome, a rare autosomal recessive disease characterized by a near absence of adipose tissue and severe insulin resistance. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. Naturally occurring read-through transcription occurs between this locus and the neighboring locus HNRNPUL2 (heterogeneous nuclear ribonucleoprotein U-like 2).[provided by RefSeq, Mar 2011]

Gene Name: BSCL2, Seipin Lipid Droplet Biogenesis Associated

Chromosome: CHR11: 62457733 -62477091

Locus: 11q12.3

Gene Diseases

The C11ORF48 BSCL2 Fusion has been associated with the following diseases:

Disease Name
Brain Lower Grade Glioma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.