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Gene-specific Copy Number Variation Probe-BCL2L11

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Catalog: CNVFP-BCL2L11-01440
Classification: Copy Number Variation
Description: Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (BCL2L11). 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: BCL2L11 Gene-specific copy number variation probes are mainly used to detect the copy number variation related to BCL2L11 genes. This product achieves the purpose of detection by hybridizing with the BCL2L11 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 BCL2 Like 11
Gene Summary [Provided by RefSeq] The protein encoded by this gene belongs to the BCL-2 protein family. BCL-2 family members form hetero- or homodimers and act as anti- or pro-apoptotic regulators that are involved in a wide variety of cellular activities. The protein encoded by this gene contains a Bcl-2 homology domain 3 (BH3). It has been shown to interact with other members of the BCL-2 protein family and to act as an apoptotic activator. The expression of this gene can be induced by nerve growth factor (NGF), as well as by the forkhead transcription factor FKHR-L1, which suggests a role of this gene in neuronal and lymphocyte apoptosis. Transgenic studies of the mouse counterpart suggested that this gene functions as an essential initiator of apoptosis in thymocyte-negative selection. Several alternatively spliced transcript variants of this gene have been identified. [provided by RefSeq, Jun 2013]
Gene Symbol BCL2L11
Location 2q13
Chromosome Chromosome2
Coordinates This gene maps to 111878490-111926022 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR CNVFP-BCL2L11-01440-OR 573nm 548nm
2 RE CNVFP-BCL2L11-01440-RE 599nm 580nm
3 GO CNVFP-BCL2L11-01440-GO 551nm 525nm
4 GR CNVFP-BCL2L11-01440-GR 515nm 491nm
5 AQ CNVFP-BCL2L11-01440-AQ 467nm 418nm

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