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MEIS2-BBS2 Fusion FISH Probe

The MEIS2-BBS2 Fusion FISH Probe is used to confirm a fusion of the MEIS2 and BBS2 genes. The fusion of the MEIS2 and BBS2 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
MEIS2-BBS2-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
MEIS2-BBS2-20-RERE 20 (40 μL) 200 μL
MEIS2-BBS2-20-REOR 20 (40 μL) 200 μL
MEIS2-BBS2-20-REGO 20 (40 μL) 200 μL
MEIS2-BBS2-20-REGR 20 (40 μL) 200 μL
MEIS2-BBS2-20-REAQ 20 (40 μL) 200 μL
MEIS2-BBS2-20-ORRE 20 (40 μL) 200 μL
MEIS2-BBS2-20-OROR 20 (40 μL) 200 μL
MEIS2-BBS2-20-ORGO 20 (40 μL) 200 μL
MEIS2-BBS2-20-ORAQ 20 (40 μL) 200 μL
MEIS2-BBS2-20-GORE 20 (40 μL) 200 μL
MEIS2-BBS2-20-GOOR 20 (40 μL) 200 μL
MEIS2-BBS2-20-GOGO 20 (40 μL) 200 μL
MEIS2-BBS2-20-GOGR 20 (40 μL) 200 μL
MEIS2-BBS2-20-GOAQ 20 (40 μL) 200 μL
MEIS2-BBS2-20-GRRE 20 (40 μL) 200 μL
MEIS2-BBS2-20-GROR 20 (40 μL) 200 μL
MEIS2-BBS2-20-GRGO 20 (40 μL) 200 μL
MEIS2-BBS2-20-GRGR 20 (40 μL) 200 μL
MEIS2-BBS2-20-GRAQ 20 (40 μL) 200 μL
MEIS2-BBS2-20-AQRE 20 (40 μL) 200 μL
MEIS2-BBS2-20-AQOR 20 (40 μL) 200 μL
MEIS2-BBS2-20-AQGO 20 (40 μL) 200 μL
MEIS2-BBS2-20-AQGR 20 (40 μL) 200 μL
MEIS2-BBS2-20-AQAQ 20 (40 μL) 200 μL

BBS2 Gene Summary

This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by severe pigmentary retinopathy, obesity, polydactyly, renal malformation and cognitive disability. The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies, ciliary axonemes, and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene forms a multiprotein BBSome complex with seven other BBS proteins.[provided by RefSeq, Oct 2014]

Gene Name: Bardet-Biedl Syndrome 2

Chromosome: CHR16: 56518258 -56554008

Locus: 16q13

MEIS2 Gene Summary

This gene encodes a homeobox protein belonging to the TALE ('three amino acid loop extension') family of homeodomain-containing proteins. TALE homeobox proteins are highly conserved transcription regulators, and several members have been shown to be essential contributors to developmental programs. Multiple transcript variants encoding distinct isoforms have been described for this gene. [provided by RefSeq, Jul 2008]

Gene Name: Meis Homeobox 2

Chromosome: CHR15: 37183221 -37393500

Locus: 15q14

Gene Diseases

The MEIS2 BBS2 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.