Gene-specific Copy Number Variation Probe-POF1B
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| Catalog: |
CNVFP-POF1B-15891 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (POF1B). 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: |
POF1B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to POF1B genes. This product achieves the purpose of detection by hybridizing with the POF1B 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 |
POF1B, Actin Binding Protein |
| Gene Summary [Provided by RefSeq] |
Premature ovarian failure (POF) is characterized by primary or secondary amenorrhea in women less than 40 years old. Two POF susceptibility regions called "POF1" and "POF2" have been identified by breakpoint mapping of X-autosome translocations. POF1 extends from Xq21-qter while POF2 extends from Xq13.3 to Xq21.1. This gene, POF1B, resides in the POF2 region. This gene is expressed at trace levels in mouse prenatal ovary and is barely detectable or absent from adult ovary, in human and in the mouse respectively. This gene's expression is restricted to epithelia with its highest expression in the epidermis, and oro-pharyngeal and gastro-intestinal tracts. The protein encoded by this gene binds non-muscle actin filaments. The role this gene may play in the etiology of premature ovarian failure remains to be determined. [provided by RefSeq, Jan 2010] |
| Gene Symbol |
POF1B |
| Location |
Xq21.1 |
| Chromosome |
ChromosomeX |
| Coordinates |
This gene maps to 84532394-84634748 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-POF1B-15891-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-POF1B-15891-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-POF1B-15891-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-POF1B-15891-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-POF1B-15891-AQ |
467nm |
418nm |
|
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