FAM111B-MS4A5 Fusion FISH Probe
The FAM111B-MS4A5 Fusion FISH Probe is used to confirm a fusion of the FAM111B and MS4A5 genes. The fusion of the FAM111B and MS4A5 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| FAM111B-MS4A5-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-RERE | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-REOR | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-REGO | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-REGR | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-REAQ | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-ORRE | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-OROR | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-ORGO | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-ORAQ | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-GORE | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-GOOR | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-GOGO | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-GOGR | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-GOAQ | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-GRRE | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-GROR | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-GRGO | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-GRGR | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-GRAQ | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-AQRE | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-AQOR | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-AQGO | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-AQGR | 20 (40 μL) | 200 μL |
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| FAM111B-MS4A5-20-AQAQ | 20 (40 μL) | 200 μL |
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MS4A5 Gene Summary
This gene encodes a member of the membrane-spanning 4A gene family. Members of this nascent protein family are characterized by common structural features and similar intron/exon splice boundaries and display unique expression patterns among hematopoietic cells and nonlymphoid tissues. Though this member is not expressed in hematopoietic cells specifically, it may be involved in signal transduction like many of its related family members. The gene encoding this protein is localized to 11q12, among a cluster of family members. [provided by RefSeq, Jul 2008]
Gene Name: Membrane Spanning 4-domains A5
Chromosome: CHR11: 60197061 -60215265
Locus: 11q12.2
FAM111B Gene Summary
This gene encodes a protein with a trypsin-like cysteine/serine peptidase domain in the C-terminus. Mutations in this gene are associated with an autosomal dominant form of hereditary fibrosing poikiloderma (HFP). Affected individuals display mottled pigmentation, telangiectasia, epidermal atrophy, tendon contractures, and progressive pulmonary fibrosis. Alternative splicing results in multiple transcript variants encoding distinct isoforms. A paralog of this gene which also has a trypsin‐like peptidase domain, FAM111A, is located only 16 kb from this gene on human chromosome 11q12.1. [provided by RefSeq, Apr 2014]
Gene Name: Family With Sequence Similarity 111 Member B
Chromosome: CHR11: 58874657 -58894888
Locus: 11q12.1
Gene Diseases
The FAM111B MS4A5 Fusion has been associated with the following diseases:
| Disease Name |
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| Breast Invasive Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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