Gene-specific Copy Number Variation Probe-LITAF
Add to Cart
| Catalog: |
CNVFP-LITAF-10422 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (LITAF). 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: |
LITAF Gene-specific copy number variation probes are mainly used to detect the copy number variation related to LITAF genes. This product achieves the purpose of detection by hybridizing with the LITAF 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 |
Lipopolysaccharide Induced TNF Factor |
| Gene Summary [Provided by RefSeq] |
Lipopolysaccharide is a potent stimulator of monocytes and macrophages, causing secretion of tumor necrosis factor-alpha (TNF-alpha) and other inflammatory mediators. This gene encodes lipopolysaccharide-induced TNF-alpha factor, which is a DNA-binding protein and can mediate the TNF-alpha expression by direct binding to the promoter region of the TNF-alpha gene. The transcription of this gene is induced by tumor suppressor p53 and has been implicated in the p53-induced apoptotic pathway. Mutations in this gene cause Charcot-Marie-Tooth disease type 1C (CMT1C) and may be involved in the carcinogenesis of extramammary Paget's disease (EMPD). Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2014] |
| Gene Symbol |
LITAF |
| Location |
16p13.13 |
| Chromosome |
Chromosome16 |
| Coordinates |
This gene maps to 11641577-11681322 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-LITAF-10422-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-LITAF-10422-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-LITAF-10422-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-LITAF-10422-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-LITAF-10422-AQ |
467nm |
418nm |
|
Other Products
