Gene-specific Copy Number Variation Probe-MAL
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| Catalog: |
CNVFP-MAL-10898 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (MAL). 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: |
MAL Gene-specific copy number variation probes are mainly used to detect the copy number variation related to MAL genes. This product achieves the purpose of detection by hybridizing with the MAL 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 |
Mal, T-cell Differentiation Protein |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a highly hydrophobic integral membrane protein belonging to the MAL family of proteolipids. The protein has been localized to the endoplasmic reticulum of T-cells and is a candidate linker protein in T-cell signal transduction. In addition, this proteolipid is localized in compact myelin of cells in the nervous system and has been implicated in myelin biogenesis and/or function. The protein plays a role in the formation, stabilization and maintenance of glycosphingolipid-enriched membrane microdomains. Down-regulation of this gene has been associated with a variety of human epithelial malignancies. Alternative splicing produces four transcript variants which vary from each other by the presence or absence of alternatively spliced exons 2 and 3. [provided by RefSeq, May 2012] |
| Gene Symbol |
MAL |
| Location |
2q11.1 |
| Chromosome |
Chromosome2 |
| Coordinates |
This gene maps to 95691478-95719735 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-MAL-10898-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-MAL-10898-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-MAL-10898-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-MAL-10898-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-MAL-10898-AQ |
467nm |
418nm |
|
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