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SNTB2-CHST4 Fusion FISH Probe

The SNTB2-CHST4 Fusion FISH Probe is used to confirm a fusion of the SNTB2 and CHST4 genes. The fusion of the SNTB2 and CHST4 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.

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

SKU Test Kits Buffer Dye Color Order Now
SNTB2-CHST4-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
SNTB2-CHST4-20-RERE 20 (40 μL) 200 μL
SNTB2-CHST4-20-REOR 20 (40 μL) 200 μL
SNTB2-CHST4-20-REGO 20 (40 μL) 200 μL
SNTB2-CHST4-20-REGR 20 (40 μL) 200 μL
SNTB2-CHST4-20-REAQ 20 (40 μL) 200 μL
SNTB2-CHST4-20-ORRE 20 (40 μL) 200 μL
SNTB2-CHST4-20-OROR 20 (40 μL) 200 μL
SNTB2-CHST4-20-ORGO 20 (40 μL) 200 μL
SNTB2-CHST4-20-ORAQ 20 (40 μL) 200 μL
SNTB2-CHST4-20-GORE 20 (40 μL) 200 μL
SNTB2-CHST4-20-GOOR 20 (40 μL) 200 μL
SNTB2-CHST4-20-GOGO 20 (40 μL) 200 μL
SNTB2-CHST4-20-GOGR 20 (40 μL) 200 μL
SNTB2-CHST4-20-GOAQ 20 (40 μL) 200 μL
SNTB2-CHST4-20-GRRE 20 (40 μL) 200 μL
SNTB2-CHST4-20-GROR 20 (40 μL) 200 μL
SNTB2-CHST4-20-GRGO 20 (40 μL) 200 μL
SNTB2-CHST4-20-GRGR 20 (40 μL) 200 μL
SNTB2-CHST4-20-GRAQ 20 (40 μL) 200 μL
SNTB2-CHST4-20-AQRE 20 (40 μL) 200 μL
SNTB2-CHST4-20-AQOR 20 (40 μL) 200 μL
SNTB2-CHST4-20-AQGO 20 (40 μL) 200 μL
SNTB2-CHST4-20-AQGR 20 (40 μL) 200 μL
SNTB2-CHST4-20-AQAQ 20 (40 μL) 200 μL

SNTB2 Gene Summary

Dystrophin is a large, rod-like cytoskeletal protein found at the inner surface of muscle fibers. Dystrophin is missing in Duchenne Muscular Dystrophy patients and is present in reduced amounts in Becker Muscular Dystrophy patients. The protein encoded by this gene is a peripheral membrane protein found associated with dystrophin and dystrophin-related proteins. This gene is a member of the syntrophin gene family, which contains at least two other structurally-related genes. [provided by RefSeq, Jul 2008]

Gene Name: Syntrophin Beta 2

Chromosome: CHR16: 69221049 -69342955

Locus: 16q22.1

CHST4 Gene Summary

This gene encodes an N-acetylglucosamine 6-O sulfotransferase. The encoded enzyme transfers sulfate from 3'phosphoadenosine 5'phospho-sulfate to the 6-hydroxyl group of N-acetylglucosamine on glycoproteins. This protein is localized to the Golgi and is involved in the modification of glycan structures on ligands of the lymphocyte homing receptor L-selectin. Alternate splicing in the 5' UTR results in multiple transcript variants that encode the same protein. [provided by RefSeq, Oct 2009]

Gene Name: Carbohydrate Sulfotransferase 4

Chromosome: CHR16: 71560022 -71572493

Locus: 16q22.2

Gene Diseases

The SNTB2 CHST4 Fusion has been associated with the following diseases:

Disease Name
Breast Invasive Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.