Gene-specific Copy Number Variation Probe-TMEM2
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| Catalog: |
CNVFP-TMEM2-21036 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TMEM2). 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: |
TMEM2 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TMEM2 genes. This product achieves the purpose of detection by hybridizing with the TMEM2 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 |
Transmembrane Protein 2 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a type II transmembrane protein that belongs to the interferon-induced transmembrane (IFITM) protein superfamily. The encoded protein functions as a cell surface hyaluronidase that cleaves extracellular high molecular weight hyaluronan into intermediate size fragments before internalization and degradation in the lysosome. It also has an interferon-mediated antiviral function in humans through activation of the JAK STAT signaling pathway. The activation of this gene by transcription factor SOX4 in breast cancer cells has been shown to mediate the pathological effects of SOX4 on cancer progression. Naturally occurring mutations in this gene are associated with autosomal recessive non-syndromic hearing loss. [provided by RefSeq, Mar 2017] |
| Gene Symbol |
TMEM2 |
| Location |
9q21.13 |
| Chromosome |
Chromosome9 |
| Coordinates |
This gene maps to 74298281-74383800 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-TMEM2-21036-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TMEM2-21036-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TMEM2-21036-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TMEM2-21036-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TMEM2-21036-AQ |
467nm |
418nm |
|
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