Gene-specific Copy Number Variation Probe-TSHB
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| Catalog: |
CNVFP-TSHB-22296 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (TSHB). 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: |
TSHB Gene-specific copy number variation probes are mainly used to detect the copy number variation related to TSHB genes. This product achieves the purpose of detection by hybridizing with the TSHB 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 |
Thyroid Stimulating Hormone Beta |
| Gene Summary [Provided by RefSeq] |
The four human glycoprotein hormones chorionic gonadotropin (CG), luteinizing hormone (LH), follicle stimulating hormone (FSH), and thyroid stimulating hormone (TSH) are dimers consisting of alpha and beta subunits that are associated noncovalently. The alpha subunits of these hormones are identical, however, their beta chains are unique and confer biological specificity. Thyroid stimulating hormone functions in the control of thyroid structure and metabolism. The protein encoded by this gene is the beta subunit of thyroid stimulating hormone. Mutations in this gene are associated with congenital central and secondary hypothyroidism and Hashimoto's thyroiditis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2013] |
| Gene Symbol |
TSHB |
| Location |
1p13.2 |
| Chromosome |
Chromosome1 |
| Coordinates |
This gene maps to 115572414-115576941 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-TSHB-22296-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-TSHB-22296-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-TSHB-22296-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-TSHB-22296-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-TSHB-22296-AQ |
467nm |
418nm |
|
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