Gene-specific Copy Number Variation Probe-HNF4A
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| Catalog: |
CNVFP-HNF4A-06714 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (HNF4A). 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: |
HNF4A Gene-specific copy number variation probes are mainly used to detect the copy number variation related to HNF4A genes. This product achieves the purpose of detection by hybridizing with the HNF4A 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 |
Hepatocyte Nuclear Factor 4 Alpha |
| Gene Summary [Provided by RefSeq] |
The protein encoded by this gene is a nuclear transcription factor which binds DNA as a homodimer. The encoded protein controls the expression of several genes, including hepatocyte nuclear factor 1 alpha, a transcription factor which regulates the expression of several hepatic genes. This gene may play a role in development of the liver, kidney, and intestines. Mutations in this gene have been associated with monogenic autosomal dominant non-insulin-dependent diabetes mellitus type I. Alternative splicing of this gene results in multiple transcript variants encoding several different isoforms. [provided by RefSeq, Apr 2012] |
| Gene Symbol |
HNF4A |
| Location |
20q13.12 |
| Chromosome |
Chromosome20 |
| Coordinates |
This gene maps to 42984440-43058311 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-HNF4A-06714-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-HNF4A-06714-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-HNF4A-06714-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-HNF4A-06714-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-HNF4A-06714-AQ |
467nm |
418nm |
|
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