Gene-specific Copy Number Variation Probe-MFSD2B
Add to Cart
Catalog: |
CNVFP-MFSD2B-11195 |
Classification: |
Copy Number Variation |
Description: |
Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (MFSD2B). 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: |
MFSD2B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to MFSD2B genes. This product achieves the purpose of detection by hybridizing with the MFSD2B 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 Facilitator Superfamily Domain Containing 2B |
Gene Summary [Provided by RefSeq] |
The Major Facilitator Superfamily Domain Containing 2B (MFSD2B) gene is located on chr2:24232952 -24247145 at 2p23.3. |
Gene Symbol |
MFSD2B |
Location |
2p23.3 |
Chromosome |
Chromosome2 |
Coordinates |
This gene maps to 24232952-24247145 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-MFSD2B-11195-OR |
573nm |
548nm |
|
2 |
RE
|
CNVFP-MFSD2B-11195-RE |
599nm |
580nm |
|
3 |
GO
|
CNVFP-MFSD2B-11195-GO |
551nm |
525nm |
|
4 |
GR
|
CNVFP-MFSD2B-11195-GR |
515nm |
491nm |
|
5 |
AQ
|
CNVFP-MFSD2B-11195-AQ |
467nm |
418nm |
|
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