Gene-specific Copy Number Variation Probe-CLCF1
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| Catalog: |
CNVFP-CLCF1-02775 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (CLCF1). 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: |
CLCF1 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to CLCF1 genes. This product achieves the purpose of detection by hybridizing with the CLCF1 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 |
Cardiotrophin Like Cytokine Factor 1 |
| Gene Summary [Provided by RefSeq] |
This gene is a member of the glycoprotein (gp)130 cytokine family and encodes cardiotrophin-like cytokine factor 1 (CLCF1). CLCF1 forms a heterodimer complex with cytokine receptor-like factor 1 (CRLF1). This dimer competes with ciliary neurotrophic factor (CNTF) for binding to the ciliary neurotrophic factor receptor (CNTFR) complex, and activates the Jak-STAT signaling cascade. CLCF1 can be actively secreted from cells by forming a complex with soluble type I CRLF1 or soluble CNTFR. CLCF1 is a potent neurotrophic factor, B-cell stimulatory agent and neuroendocrine modulator of pituitary corticotroph function. Defects in CLCF1 cause cold-induced sweating syndrome 2 (CISS2). This syndrome is characterized by a profuse sweating after exposure to cold as well as congenital physical abnormalities of the head and spine. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Oct 2009] |
| Gene Symbol |
CLCF1 |
| Location |
11q13.2 |
| Chromosome |
Chromosome11 |
| Coordinates |
This gene maps to 67131638-67141648 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-CLCF1-02775-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-CLCF1-02775-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-CLCF1-02775-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-CLCF1-02775-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-CLCF1-02775-AQ |
467nm |
418nm |
|
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