Gene-specific Copy Number Variation Probe-FAM111B
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| Catalog: |
CNVFP-FAM111B-04894 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FAM111B). The product usually consists of a combination of reagents, which consists of a probe with a selected dye color and a hybridization reagent. We provide CNV FISH Probes with a variety of dye color combinations to meet various challenges. Probe products not only provide some classic color combinations but also provide customized probe services. |
| Application: |
FAM111B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FAM111B genes. This product achieves the purpose of detection by hybridizing with the FAM111B gene. Due to this design method, our probe products can detect the amplification and deletion of target genes on chromosomes through FISH. |
| Category: |
Copy Number Variation |
| Probe Kits Volume (µL): |
40 μL |
| Quantity: |
20 Tests |
| Hybridization Solution (µL): |
200 μL |
| Turnaround Time: |
7-10 Business Days |
| Shipping Time: |
1-2 Day Expedited Shipping |
| Storage Conditions: |
Store at -20℃ and avoid light; |
| Shipping Conditions: |
-20℃ |
Gene Details
| Gene Name |
Family With Sequence Similarity 111 Member B |
| Gene Summary [Provided by RefSeq] |
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 Symbol |
FAM111B |
| Location |
11q12.1 |
| Chromosome |
Chromosome11 |
| Coordinates |
This gene maps to 58874657-58894888 in GRCh37 coordinates. |
| Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
| Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
Add to Cart |
| 1 |
OR
|
CNVFP-FAM111B-04894-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FAM111B-04894-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FAM111B-04894-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FAM111B-04894-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FAM111B-04894-AQ |
467nm |
418nm |
|
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