Gene-specific Copy Number Variation Probe-DMTN
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| Catalog: |
CNVFP-DMTN-03899 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (DMTN). 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: |
DMTN Gene-specific copy number variation probes are mainly used to detect the copy number variation related to DMTN genes. This product achieves the purpose of detection by hybridizing with the DMTN 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 |
Dematin Actin Binding Protein |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is an actin binding and bundling protein that plays a structural role in erythrocytes, by stabilizing and attaching the spectrin/actin cytoskeleton to the erythrocyte membrane in a phosphorylation-dependent manner. This protein contains a core domain in the N-terminus, and a headpiece domain in the C-terminus that binds F-actin. When purified from erythrocytes, this protein exists as a trimer composed of two 48 kDa polypeptides and a 52 kDa polypeptide. The different subunits arise from alternative splicing in the 3' coding region, where the headpiece domain is located. Disruption of this gene has been correlated with the autosomal dominant Marie Unna hereditary hypotrichosis disease, while loss of heterozygosity of this gene is thought to play a role in prostate cancer progression. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Nov 2014] |
| Gene Symbol |
DMTN |
| Location |
8p21.3 |
| Chromosome |
Chromosome8 |
| Coordinates |
This gene maps to 22048954-22082526 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-DMTN-03899-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-DMTN-03899-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-DMTN-03899-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-DMTN-03899-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-DMTN-03899-AQ |
467nm |
418nm |
|
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