Gene-specific Copy Number Variation Probe-TNFRSF1A
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Catalog: |
CNVFP-TNFRSF1A-21217 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TNFRSF1A). 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: |
TNFRSF1A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TNFRSF1A genes. This product achieves the purpose of detection by hybridizing with the TNFRSF1A 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 |
TNF Receptor Superfamily Member 1A |
Gene Summary [Provided by RefSeq] |
This gene encodes a member of the TNF receptor superfamily of proteins. The encoded receptor is found in membrane-bound and soluble forms that interact with membrane-bound and soluble forms, respectively, of its ligand, tumor necrosis factor alpha. Binding of membrane-bound tumor necrosis factor alpha to the membrane-bound receptor induces receptor trimerization and activation, which plays a role in cell survival, apoptosis, and inflammation. Proteolytic processing of the encoded receptor results in release of the soluble form of the receptor, which can interact with free tumor necrosis factor alpha to inhibit inflammation. Mutations in this gene underlie tumor necrosis factor receptor-associated periodic syndrome (TRAPS), characterized by fever, abdominal pain and other features. Mutations in this gene may also be associated with multiple sclerosis in human patients. [provided by RefSeq, Sep 2016] |
Gene Symbol |
TNFRSF1A |
Location |
12p13.31 |
Chromosome |
Chromosome12 |
Coordinates |
This gene maps to 6437922-6451283 in GRCh37 coordinates. |
Species |
Human |
Dye Colors:
OR
RE
GO
GR
AQ
Order Sheet
Number |
Dye Color |
Order Name |
Absorbance Maximum |
Emission Maximum |
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1 |
OR
|
CNVFP-TNFRSF1A-21217-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-TNFRSF1A-21217-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-TNFRSF1A-21217-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-TNFRSF1A-21217-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-TNFRSF1A-21217-AQ |
467nm |
418nm |
|
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