Gene-specific Copy Number Variation Probe-SSB
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| Catalog: |
CNVFP-SSB-19885 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SSB). 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: |
SSB Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SSB genes. This product achieves the purpose of detection by hybridizing with the SSB 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 |
Sjogren Syndrome Antigen B |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is involved in diverse aspects of RNA metabolism, including binding and protecting poly(U) termini of nascent RNA polymerase III transcripts from exonuclease digestion, processing 5' and 3' ends of pre-tRNA precursors, acting as an RNA chaperone, and binding viral RNAs associated with hepatitis C virus. Autoantibodies reacting with this protein are found in the sera of patients with Sjogren syndrome and systemic lupus erythematosus. Alternative promoter usage results in two different transcript variants which encode the same protein. [provided by RefSeq, Jun 2014] |
| Gene Symbol |
SSB |
| Location |
2q31.1 |
| Chromosome |
Chromosome2 |
| Coordinates |
This gene maps to 170655388-170668575 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-SSB-19885-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-SSB-19885-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-SSB-19885-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-SSB-19885-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-SSB-19885-AQ |
467nm |
418nm |
|
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