Gene-specific Copy Number Variation Probe-RRBP1
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| Catalog: |
CNVFP-RRBP1-17774 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (RRBP1). 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: |
RRBP1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to RRBP1 genes. This product achieves the purpose of detection by hybridizing with the RRBP1 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 |
Ribosome Binding Protein 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a ribosome-binding protein of the endoplasmic reticulum (ER) membrane. Studies suggest that this gene plays a role in ER proliferation, secretory pathways and secretory cell differentiation, and mediation of ER-microtubule interactions. Alternative splicing has been observed and protein isoforms are characterized by regions of N-terminal decapeptide and C-terminal heptad repeats. Splicing of the tandem repeats results in variations in ribosome-binding affinity and secretory function. The full-length nature of variants which differ in repeat length has not been determined. Pseudogenes of this gene have been identified on chromosomes 3 and 7, and RRBP1 has been excluded as a candidate gene in the cause of Alagille syndrome, the result of a mutation in a nearby gene on chromosome 20p12. [provided by RefSeq, Apr 2012] |
| Gene Symbol |
RRBP1 |
| Location |
20p12.1 |
| Chromosome |
Chromosome20 |
| Coordinates |
This gene maps to 17594322-17662928 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-RRBP1-17774-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-RRBP1-17774-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-RRBP1-17774-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-RRBP1-17774-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-RRBP1-17774-AQ |
467nm |
418nm |
|
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