Gene-specific Copy Number Variation Probe-TNXB
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| Catalog: |
CNVFP-TNXB-21149 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TNXB). 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: |
TNXB Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TNXB genes. This product achieves the purpose of detection by hybridizing with the TNXB 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 |
Tenascin XB |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the tenascin family of extracellular matrix glycoproteins. The tenascins have anti-adhesive effects, as opposed to fibronectin which is adhesive. This protein is thought to function in matrix maturation during wound healing, and its deficiency has been associated with the connective tissue disorder Ehlers-Danlos syndrome. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. It is one of four genes in this cluster which have been duplicated. The duplicated copy of this gene is incomplete and is a pseudogene which is transcribed but does not encode a protein. The structure of this gene is unusual in that it overlaps the CREBL1 and CYP21A2 genes at its 5' and 3' ends, respectively. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
TNXB |
| Location |
6p21.33-p21.32 |
| Chromosome |
Chromosome6_cox_hap2 |
| Coordinates |
This gene maps to 3479582-3547813 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-TNXB-21149-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TNXB-21149-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TNXB-21149-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TNXB-21149-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TNXB-21149-AQ |
467nm |
418nm |
|
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