Gene-specific Copy Number Variation Probe-HNF1B
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| Catalog: |
CNVFP-HNF1B-06716 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (HNF1B). 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: |
HNF1B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to HNF1B genes. This product achieves the purpose of detection by hybridizing with the HNF1B 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 |
HNF1 Homeobox B |
| Gene Summary [Provided by RefSeq] |
This gene encodes a member of the homeodomain-containing superfamily of transcription factors. The protein binds to DNA as either a homodimer, or a heterodimer with the related protein hepatocyte nuclear factor 1-alpha. The gene has been shown to function in nephron development, and regulates development of the embryonic pancreas. Mutations in this gene result in renal cysts and diabetes syndrome and noninsulin-dependent diabetes mellitus, and expression of this gene is altered in some types of cancer. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009] |
| Gene Symbol |
HNF1B |
| Location |
17q12 |
| Chromosome |
Chromosome17 |
| Coordinates |
This gene maps to 36046433-36105096 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-HNF1B-06716-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-HNF1B-06716-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-HNF1B-06716-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-HNF1B-06716-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-HNF1B-06716-AQ |
467nm |
418nm |
|
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