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Gene-specific Copy Number Variation Probe-SPAG11B

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Catalog: CNVFP-SPAG11B-19805
Classification: Copy Number Variation
Description: Our Gene-specific Copy Number Variation Probes usually target the flanks of the target gene (SPAG11B). 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: SPAG11B Gene-specific copy number variation probes are mainly used to detect the copy number variation related to SPAG11B genes. This product achieves the purpose of detection by hybridizing with the SPAG11B 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 Sperm Associated Antigen 11B
Gene Summary [Provided by RefSeq] This gene encodes several androgen-dependent, epididymis-specific secretory proteins. The specific functions of these proteins have not been determined, but they are thought to be involved in sperm maturation. Some of the isoforms contain regions of similarity to beta-defensins, a family of antimicrobial peptides. The gene is located on chromosome 8p23 near the defensin gene cluster. Alternative splicing of this gene results in seven transcript variants encoding different isoforms. Two different N-terminal and five different C-terminal protein sequences are encoded by the splice variants. Two additional variants have been described, but their full length sequences have not been determined. [provided by RefSeq, Jul 2008]
Gene Symbol SPAG11B
Location 8p23.1
Chromosome Chromosome8
Coordinates This gene maps to 7305275-7321192 in GRCh37 coordinates.
Species Human

Order Sheet

Number Dye Color Order Name Absorbance Maximum Emission Maximum Add to Cart
1 OR CNVFP-SPAG11B-19805-OR 573nm 548nm
2 RE CNVFP-SPAG11B-19805-RE 599nm 580nm
3 GO CNVFP-SPAG11B-19805-GO 551nm 525nm
4 GR CNVFP-SPAG11B-19805-GR 515nm 491nm
5 AQ CNVFP-SPAG11B-19805-AQ 467nm 418nm

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