Gene-specific Copy Number Variation Probe-FHOD1
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| Catalog: |
CNVFP-FHOD1-05449 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (FHOD1). 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: |
FHOD1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to FHOD1 genes. This product achieves the purpose of detection by hybridizing with the FHOD1 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 |
Formin Homology 2 Domain Containing 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a protein which is a member of the formin/diaphanous family of proteins. The gene is ubiquitously expressed but is found in abundance in the spleen. The encoded protein has sequence homology to diaphanous and formin proteins within the Formin Homology (FH)1 and FH2 domains. It also contains a coiled-coil domain, a collagen-like domain, two nuclear localization signals, and several potential PKC and PKA phosphorylation sites. It is a predominantly cytoplasmic protein and is expressed in a variety of human cell lines. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015] |
| Gene Symbol |
FHOD1 |
| Location |
16q22.1 |
| Chromosome |
Chromosome16 |
| Coordinates |
This gene maps to 67263291-67281425 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-FHOD1-05449-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-FHOD1-05449-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-FHOD1-05449-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-FHOD1-05449-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-FHOD1-05449-AQ |
467nm |
418nm |
|
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