Gene-specific Copy Number Variation Probe-CFC1
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| Catalog: |
CNVFP-CFC1-02660 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CFC1). 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: |
CFC1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CFC1 genes. This product achieves the purpose of detection by hybridizing with the CFC1 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 |
Cripto, FRL-1, Cryptic Family 1 |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the epidermal growth factor (EGF)- Cripto, Frl-1, and Cryptic (CFC) family, which are involved in signalling during embryonic development. Proteins in this family share a variant EGF-like motif, a conserved cysteine-rich domain, and a C-terminal hydrophobic region. The protein encoded by this gene is necessary for patterning the left-right embryonic axis. Mutations in this gene are associated with defects in organ development, including autosomal visceral heterotaxy and congenital heart disease. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012] |
| Gene Symbol |
CFC1 |
| Location |
2q21.1 |
| Chromosome |
Chromosome2 |
| Coordinates |
This gene maps to 131350334-131357082 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-CFC1-02660-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CFC1-02660-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CFC1-02660-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CFC1-02660-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CFC1-02660-AQ |
467nm |
418nm |
|
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