Gene-specific Copy Number Variation Probe-HLA-F
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| Catalog: |
CNVFP-HLA-F-06785 |
| Classification: |
Copy Number Variation |
| Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (HLA-F). 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: |
HLA-F Gene-specific copy number variation probes are mainly used to detect the copy number variation related to HLA-F genes. This product achieves the purpose of detection by hybridizing with the HLA-F 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 |
Major Histocompatibility Complex, Class I, F |
| Gene Summary [Provided by RefSeq] |
This gene belongs to the HLA class I heavy chain paralogues. It encodes a non-classical heavy chain that forms a heterodimer with a beta-2 microglobulin light chain, with the heavy chain anchored in the membrane. Unlike most other HLA heavy chains, this molecule is localized in the endoplasmic reticulum and Golgi apparatus, with a small amount present at the cell surface in some cell types. It contains a divergent peptide-binding groove, and is thought to bind a restricted subset of peptides for immune presentation. This gene exhibits few polymorphisms. Multiple transcript variants encoding different isoforms have been found for this gene. These variants lack a coding exon found in transcripts from other HLA paralogues due to an altered splice acceptor site, resulting in a shorter cytoplasmic domain. [provided by RefSeq, Jul 2008] |
| Gene Symbol |
HLA-F |
| Location |
6p22.1 |
| Chromosome |
Chromosome6_mcf_hap5 |
| Coordinates |
This gene maps to 991650-1359214 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-HLA-F-06785-OR |
573nm |
548nm |
|
| 2 |
RE
|
CNVFP-HLA-F-06785-RE |
599nm |
580nm |
|
| 3 |
GO
|
CNVFP-HLA-F-06785-GO |
551nm |
525nm |
|
| 4 |
GR
|
CNVFP-HLA-F-06785-GR |
515nm |
491nm |
|
| 5 |
AQ
|
CNVFP-HLA-F-06785-AQ |
467nm |
418nm |
|
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