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SEMA3D-RBM28 Fusion FISH Probe

The SEMA3D-RBM28 Fusion FISH Probe is used to confirm a fusion of the SEMA3D and RBM28 genes. The fusion of the SEMA3D and RBM28 genes has been associated with Prostate Adenocarcinoma. 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
SEMA3D-RBM28-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
SEMA3D-RBM28-20-RERE 20 (40 μL) 200 μL
SEMA3D-RBM28-20-REOR 20 (40 μL) 200 μL
SEMA3D-RBM28-20-REGO 20 (40 μL) 200 μL
SEMA3D-RBM28-20-REGR 20 (40 μL) 200 μL
SEMA3D-RBM28-20-REAQ 20 (40 μL) 200 μL
SEMA3D-RBM28-20-ORRE 20 (40 μL) 200 μL
SEMA3D-RBM28-20-OROR 20 (40 μL) 200 μL
SEMA3D-RBM28-20-ORGO 20 (40 μL) 200 μL
SEMA3D-RBM28-20-ORAQ 20 (40 μL) 200 μL
SEMA3D-RBM28-20-GORE 20 (40 μL) 200 μL
SEMA3D-RBM28-20-GOOR 20 (40 μL) 200 μL
SEMA3D-RBM28-20-GOGO 20 (40 μL) 200 μL
SEMA3D-RBM28-20-GOGR 20 (40 μL) 200 μL
SEMA3D-RBM28-20-GOAQ 20 (40 μL) 200 μL
SEMA3D-RBM28-20-GRRE 20 (40 μL) 200 μL
SEMA3D-RBM28-20-GROR 20 (40 μL) 200 μL
SEMA3D-RBM28-20-GRGO 20 (40 μL) 200 μL
SEMA3D-RBM28-20-GRGR 20 (40 μL) 200 μL
SEMA3D-RBM28-20-GRAQ 20 (40 μL) 200 μL
SEMA3D-RBM28-20-AQRE 20 (40 μL) 200 μL
SEMA3D-RBM28-20-AQOR 20 (40 μL) 200 μL
SEMA3D-RBM28-20-AQGO 20 (40 μL) 200 μL
SEMA3D-RBM28-20-AQGR 20 (40 μL) 200 μL
SEMA3D-RBM28-20-AQAQ 20 (40 μL) 200 μL

RBM28 Gene Summary

The protein encoded by this gene is a specific nucleolar component of the spliceosomal small nuclear ribonucleoprotein (snRNP)complexes . It specifically associates with U1, U2, U4, U5, and U6 small nuclear RNAs (snRNAs), possibly coordinating their transition through the nucleolus. Mutation in this gene causes alopecia, progressive neurological defects, and endocrinopathy (ANE syndrome), a pleiotropic and clinically heterogeneous disorder. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]

Gene Name: RNA Binding Motif Protein 28

Chromosome: CHR7: 127950435 -127983962

Locus: 7q32.1

SEMA3D Gene Summary

This gene encodes a member of the semaphorin III family of secreted signaling proteins that are involved in axon guidance during neuronal development. The encoded protein contains an N-terminal Sema domain, an immunoglobulin like domain and a C-terminal basic domain. The protein encoded by this gene binds neuropilin and plays an important role in cardiovascular development. [provided by RefSeq, Aug 2016]

Gene Name: Semaphorin 3D

Chromosome: CHR7: 84624871 -84751247

Locus: 7q21.11

Gene Diseases

The SEMA3D RBM28 Fusion has been associated with the following diseases:

Disease Name
Prostate Adenocarcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.